| Year |
Citation |
Score |
| 2020 |
Ohkubo Y, Akasaka K, Masuda Y, Konishi S, Yang CY, Takikawa H, Mori K. Pheromone synthesis. Part 265: Synthesis and stereochemical composition of two pheromonal compounds of the female Korean apricot wasp, Eurytoma maslovskii Tetrahedron. 76: 131410. DOI: 10.1016/J.Tet.2020.131410 |
0.395 |
|
| 2017 |
Mori K, Tabata J. Pheromone synthesis. Part 262: Determination of the absolute configuration of the female sex pheromone [(1 S ,2 S )-(−)-(1,2-dimethyl-3-methylenecyclopentyl) acetaldehyde] of the pineapple mealybug ( Dysmicoccus brevipes ) by synthesis coupled with X-ray analysis Tetrahedron. 73: 6530-6541. DOI: 10.1016/J.Tet.2017.09.046 |
0.401 |
|
| 2016 |
Szczerbowski D, Torrens GG, Rodrigues MACM, Trevisan O, Gomes SMS, Tröger A, Mori K, Francke W, Zarbin PHG. (1R,6R)-2,2,6-Trimethyl-3-oxabicyclo[4.2.0]octan-4-one, a new monoterpene lactone produced by males of the cocoa borer Conotrachelus humeropictus (Col.: Curculionidae) Tetrahedron Letters. 57: 2842-2844. DOI: 10.1016/J.Tetlet.2016.05.036 |
0.351 |
|
| 2015 |
Sakai T, Matsushita S, Arakawa S, Mori K, Tanimoto M, Tokumasu A, Yoshida T, Mori Y. Total Synthesis of Gymnocin-A. Journal of the American Chemical Society. PMID 26521846 DOI: 10.1021/jacs.5b10082 |
0.31 |
|
| 2015 |
Mori N, Kitahara T, Mori K, Watanabe H. Asymmetric Formal Synthesis of Azadirachtin. Angewandte Chemie (International Ed. in English). PMID 26474211 DOI: 10.1002/Anie.201507935 |
0.764 |
|
| 2015 |
Mori K, Miyake A, Akiyama T. Enantioselective synthesis of fused heterocycles with contiguous stereogenic centers by chiral phosphoric acid catalyzed symmetry breaking. Chemical Communications (Cambridge, England). PMID 26392151 DOI: 10.1039/c5cc05508c |
0.339 |
|
| 2015 |
Mori K, Akasaka K. Pheromone synthesis. Part 258. Synthesis of the enantiomers of the beetle pheromones ethyl 4-methylheptanoate, 4-methyloctanoic acid and 4-methyl-1-nonanol, and HPLC analysis of their derivatives to determine their enantiomeric purities Tetrahedron Asymmetry. DOI: 10.1016/J.Tetasy.2016.01.014 |
0.416 |
|
| 2015 |
Mori K, Osada K, Amaike M. Mammalian blood odorant and chirality: synthesis and sensory evaluation by humans and mice of the racemate and enantiomers of trans-4,5-epoxy-(E)-2-decenal Tetrahedron Asymmetry. 26: 861-867. DOI: 10.1016/J.Tetasy.2015.06.011 |
0.354 |
|
| 2015 |
Mori K, Akasaka K. Pheromone synthesis. Part 256: Synthesis of the four stereoisomers of 5,11-dimethylpentacosane, a new sex pheromone component of the male Galleria mellonella (L.), with high stereochemical purities as determined by the derivatization-HPLC analysis of the eight stereoisomers of 5,11-dimethyl-8-pentacosanol Tetrahedron. 71: 4102-4115. DOI: 10.1016/J.Tet.2015.04.107 |
0.423 |
|
| 2015 |
Vuts J, Francke W, Mori K, Zarbin PHG, Hooper AM, Millar JG, Pickett JA, Tõth M, Chamberlain K, Caulfield JC, Woodcock CM, Tröger AG, Csonka ÉB, Birkett MA. Pheromone Bouquet of the Dried Bean Beetle, Acanthoscelides obtectus (Col.: Chrysomelidae), Now Complete European Journal of Organic Chemistry. 2015: 4843-4846. DOI: 10.1002/Ejoc.201500196 |
0.332 |
|
| 2014 |
Mori K. Stereochemical aspects of pheromonal communications: diversity is the key word. Journal of Chemical Ecology. 40: 214. PMID 24619726 DOI: 10.1007/S10886-014-0396-2 |
0.46 |
|
| 2014 |
Mori K, Akasaka K, Matsunaga S. Chemoenzymatic synthesis and HPLC analysis of the stereoisomers of miyakosyne A [(4E,24E)-14-methyloctacosa-4,24-diene-1,27-diyne-3,26-diol], a cytotoxic metabolite of a marine sponge Petrosia sp., to determine the absolute configuration of its major component as 3R,14R,26R Tetrahedron. 70: 392-401. DOI: 10.1016/J.Tet.2013.11.045 |
0.333 |
|
| 2013 |
Dunkelblum E, Gries R, Gries G, Mori K, Mendel Z. Chirality of israeli pine bast scale,Matsucoccus josephi (homoptera: Matsucoccidae) sex pheromone. Journal of Chemical Ecology. 21: 849-58. PMID 24234322 DOI: 10.1007/Bf02033465 |
0.34 |
|
| 2013 |
James DG, Mori K. Spined citrus bugs,Biprorulus bibax breddin (Hemiptera: Pentatomidae), do not discriminate between enantiomers in their aggregation pheromone. Journal of Chemical Ecology. 21: 403-6. PMID 24234171 DOI: 10.1007/Bf02036737 |
0.365 |
|
| 2013 |
Shikichi Y, Shankar S, Yew JY, Mori K. Synthesis and bioassay of the eight analogues of the CH503 male pheromone (3-acetoxy-11,19-octacosadien-1-ol) of the Drosophila melanogaster fruit fly. Bioscience, Biotechnology, and Biochemistry. 77: 1931-8. PMID 24018690 DOI: 10.1271/Bbb.130383 |
0.331 |
|
| 2013 |
Tashiro T, Nakagawa R, Shigeura T, Watarai H, Taniguchi M, Mori K. RCAI-61 and related 6'-modified analogs of KRN7000: their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo. Bioorganic & Medicinal Chemistry. 21: 3066-79. PMID 23602521 DOI: 10.1016/J.Bmc.2013.03.028 |
0.323 |
|
| 2013 |
Tashiro T, Shigeura T, Shiozaki M, Watarai H, Taniguchi M, Mori K. RCAI-133, an N-methylated analogue of KRN7000, activates mouse natural killer T cells to produce Th2-biased cytokines Medchemcomm. 4: 949. DOI: 10.1039/C3Md00073G |
0.319 |
|
| 2012 |
Shikichi Y, Mori K. Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, sex pheromone components of the Lyclene dharma dharma moth, from the enantiomers of citronellal. Bioscience, Biotechnology, and Biochemistry. 76: 1943-51. PMID 23047114 DOI: 10.1271/Bbb.120436 |
0.379 |
|
| 2012 |
Tashiro T, Mori K. Synthesis of sphingolipids with an ω-esterified long acyl chain, ceramide components of the human epidermis. Bioscience, Biotechnology, and Biochemistry. 76: 1715-20. PMID 22972337 DOI: 10.1271/Bbb.120333 |
0.39 |
|
| 2012 |
Shikichi Y, Mori K. Synthesis of (1R,7Z)-1-methyl-7-hexadecenyl acetate, the female sex pheromone of the honey locust gall midge. Bioscience, Biotechnology, and Biochemistry. 76: 1419-21. PMID 22785491 DOI: DN/JST.JSTAGE/bbb/120265 |
0.339 |
|
| 2012 |
Tashiro T, Shigeura T, Watarai H, Taniguchi M, Mori K. RCAI-84, 91, and 105-108, ureido and thioureido analogs of KRN7000: their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines. Bioorganic & Medicinal Chemistry. 20: 4540-8. PMID 22739091 DOI: 10.1016/J.Bmc.2012.05.073 |
0.3 |
|
| 2012 |
Shikichi Y, Mori K. Metathesis-mediated synthesis of (R)-10-methyl-2-tridecanone, the southern corn rootworm pheromone. Bioscience, Biotechnology, and Biochemistry. 76: 407-9. PMID 22313781 DOI: 10.1271/Bbb.110738 |
0.444 |
|
| 2012 |
Kuhar TP, Hitchner EM, Youngman RR, Mori K, Dickens JC. Field response of Colorado potato beetle to enantiomeric blends of CPB I aggregation pheromone Agricultural Sciences. 3: 896-899. DOI: 10.4236/As.2012.37108 |
0.37 |
|
| 2012 |
Shikichi Y, Akasaka K, Tamogami S, Shankar S, Yew JY, Mori K. Pheromone synthesis. Part 250: Determination of the stereostructure of CH503, a sex pheromone of male Drosophila melanogaster, as (3R,11Z,19Z)-3- acetoxy-11,19-octacosadien-1-ol by synthesis and chromatographic analysis of its eight isomers Tetrahedron. 68: 3750-3760. DOI: 10.1016/J.Tet.2012.03.002 |
0.372 |
|
| 2011 |
Lu Y, Beeman RW, Campbell JF, Park Y, Aikins MJ, Mori K, Akasaka K, Tamogami S, Phillips TW. Anatomical localization and stereoisomeric composition of Tribolium castaneum aggregation pheromones. Die Naturwissenschaften. 98: 755-61. PMID 21814811 DOI: 10.1007/S00114-011-0824-X |
0.361 |
|
| 2011 |
Mori K, Tashiro T. Sphingolipids and glycosphingolipids: their syntheses and bioactivities Heterocycles. 83: 951-1003. DOI: 10.3987/Rev-10-689 |
0.373 |
|
| 2011 |
Marques FA, Zaleski SRM, Lazzari SMN, Frensch G, Senhorini GA, Maia BHLNS, Tröger A, Francke W, Iede ET, Mori K. Identification of (1R, 2S)-grandisal and (1R, 2S)-grandisol in Pissodes castaneus male-produced volatiles: evidence of a sex pheromone Journal of the Brazilian Chemical Society. 22: 1050-1055. DOI: 10.1590/S0103-50532011000600007 |
0.329 |
|
| 2011 |
Akasaka K, Tamogami S, Beeman RW, Mori K. Pheromone synthesis. Part 245: Synthesis and chromatographic analysis of the four stereoisomers of 4,8-dimethyldecanal, the male aggregation pheromone of the red flour beetle, Tribolium castaneum Tetrahedron. 67: 201-209. DOI: 10.1016/J.Tet.2010.10.086 |
0.394 |
|
| 2010 |
Shiozaki M, Tashiro T, Koshino H, Nakagawa R, Inoue S, Shigeura T, Watarai H, Taniguchi M, Mori K. Synthesis and biological activity of ester and ether analogues of alpha-galactosylceramide (KRN7000). Carbohydrate Research. 345: 1663-84. PMID 20591421 DOI: 10.1016/J.Carres.2010.05.003 |
0.306 |
|
| 2010 |
Zarbin PH, Moreira MA, Haftmann J, Tröger A, Franke S, Kopf J, Mori K, Francke W. (1R,2S,6R)-2-Hydroxymethyl-2,6-dimethyl-3-oxabicyclo[4.2.0]octane, a new volatile released by males of the papaya borer Pseudopiazurus obesus (Col.: Curculionidae). Organic Letters. 12: 2447-9. PMID 20465270 DOI: 10.1021/Ol100074Q |
0.35 |
|
| 2010 |
Mori K, Tashiro T, Zhao B, Suckling DM, El-Sayed AM. Pheromone synthesis. Part 243: Synthesis and biological evaluation of (3R,13R,1′S)-1′-ethyl-2′-methylpropyl 3,13-dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegata, and its stereoisomers Tetrahedron. 66: 2642-2653. DOI: 10.1016/J.Tet.2010.02.028 |
0.461 |
|
| 2010 |
Kurosawa S, Bando M, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 212. Synthesis of (1R,4R,5S)-(+)-Acoradiene, the Structure Proposed for the Aggregation Pheromone of the Broad-Horned Flour Beetle. Cheminform. 33: no-no. DOI: 10.1002/chin.200218218 |
0.317 |
|
| 2010 |
Okochi T, Mori K. ChemInform Abstract: Synthesis of Compounds with Juvenile Hormone Activity. Part 32. New Enantioselective Synthesis of (10R,11S)-(+)-Juvenile Hormones I (Va) and II (Vb). Cheminform. 33: no-no. DOI: 10.1002/chin.200211199 |
0.316 |
|
| 2010 |
Fujita K, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 206. Synthesis of (2R,4R)-Supellapyrone, the Sex Pheromone of the Brownbanded Cockroach, Supella longipalpa, and Its Three Stereoisomers. Cheminform. 33: no-no. DOI: 10.1002/chin.200209249 |
0.319 |
|
| 2010 |
Tanada Y, Mori K. ChemInform Abstract: Synthetic Microbial Chemistry. Part 36. Synthesis and Absolute Configuration of (-)-Neuchromenin (I), a Neurotrophic Metabolite of Eupenicillium javanicum var. meloforme, and Its Enantiomer. Cheminform. 33: no-no. DOI: 10.1002/chin.200209236 |
0.332 |
|
| 2010 |
Kurosawa S, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 200. Synthesis of (S)-9-Methylgermacrene-B, the Male-Produced Sex Pheromone of the Sandfly Lutzomyia longipalpis from Lapinha, Brazil, and Its (R)-Isomer. Cheminform. 31: no-no. DOI: 10.1002/chin.200020212 |
0.346 |
|
| 2010 |
Tashiro T, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 197. Synthesis of the Enantiomers of 2-sec-Butyl-4,5-dihydrothiazole and (1R,5S,7R)-3,4-Dehydro-exo-brevicomin, Pheromone Components of the Male Mouse, Mus musculus. Cheminform. 30: no-no. DOI: 10.1002/chin.199950229 |
0.336 |
|
| 2010 |
Sano S, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 195. Synthesis of (1R*,3R*,7R*)-3-Methyl-α-himachalene, the Racemate of the Male-Produced Sex Pheromone of the Sandfly Lutzomyia longipalpis from Jacobina, Brazil. Cheminform. 30: no-no. DOI: 10.1002/chin.199941262 |
0.31 |
|
| 2010 |
Domon K, Takikawa H, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 194. Synthesis of the Enantiomers of (Z)-21-Methyl-8-pentatriacontene, the Major Component of the Female-Produced Contact Sex Pheromone of the Yellow-Spotted Longicorn Beetle, Psacothea hilaris. Cheminform. 30: no-no. DOI: 10.1002/chin.199930246 |
0.303 |
|
| 2010 |
Domon K, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 193. Simple Synthesis of (.+-.)-Stigmolone (8-Hydroxy-2,5,8-trimethyl-4-nonanone), the Pheromone of Stigmatella aurantiaca. Cheminform. 30: no-no. DOI: 10.1002/chin.199930245 |
0.367 |
|
| 2010 |
Tamagawa H, Takikawa H, Mori K. ChemInform Abstract: Pheromone Synthesis. Part 192. Synthesis of All the Stereoisomers of 10,14-Dimethyloctadec-1-ene, 5,9-Dimethyloctadecane and 5,9-Dimethylheptadecane, the Sex Pheromone Components of the Apple Leafminer, Lyonetia prunifoliella. Cheminform. 30: no-no. DOI: 10.1002/chin.199930244 |
0.327 |
|
| 2010 |
Horiuchi S, Takikawa H, Mori K. ChemInform Abstract: Synthesis of Mono- and Sesquiterpenoids. Part 27. Synthesis of (6S,7S)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one (IV), the Opposite Enantiomer of the Antibacterial Sesquiterpene from Premna oligotricha, and the (R) Enantiomer (IX) of Cheminform. 30: no-no. DOI: 10.1002/chin.199916193 |
0.381 |
|
| 2010 |
TAKIKAWA H, TAMAGAWA H, MORI K. ChemInform Abstract: Pheromone Synthesis. Part 189. Synthesis of the Enantiomers of 6-Methyl-3-nonanone, the Female-Produced Sex Pheromone of Caddisfly, Hesperophylax occidentalis. Cheminform. 30: no-no. DOI: 10.1002/chin.199905241 |
0.315 |
|
| 2010 |
KINOSHITA Y, WATANABE H, KITAHARA T, MORI K. ChemInform Abstract: Concise Construction of N-Alkylated Phenazinone Skeletons: Synthesis of Lavanducyanin (WS-9659A). Cheminform. 26: no-no. DOI: 10.1002/chin.199521171 |
0.715 |
|
| 2010 |
WATANABE H, SHIMIZU H, MORI K. ChemInform Abstract: Synthesis of Compounds with Juvenile Hormone Activity. Part 31. Stereocontrolled Synthesis of (+)-Juvabione (VII) from a Chiral Sulfoxide. Cheminform. 26: no-no. DOI: 10.1002/chin.199515235 |
0.324 |
|
| 2010 |
MORI K, AMAIKE M, OLIVER JE. ChemInform Abstract: Pheromone Synthesis. Part 143. Synthesis and Absolute Configuration of the Hemiacetal Pheromone of the Spined Citrus Bug Biprorulus bibax. Cheminform. 24: no-no. DOI: 10.1002/chin.199312266 |
0.351 |
|
| 2010 |
KITAHARA T, KIYOTA H, KURATA H, MORI K. ChemInform Abstract: Synthesis of Mono- and Sesquiterpenoids. Part 20. Synthesis of Oxygenated Eremophilanes, Gigantenone, Phomenone and Phaseolinone, Phytotoxins from Pathogenic Fungi. Cheminform. 22: no-no. DOI: 10.1002/chin.199124205 |
0.624 |
|
| 2010 |
KITAHARA T, MIYAKE M, KIDO M, MORI K. ChemInform Abstract: Preparative Bioorganic Chemistry. Part 13. A Chiral Building Block with Bicyclo(2.2.2)octanone Skeleton by the Reduction with Baker′s Yeast. Cheminform. 22: no-no. DOI: 10.1002/chin.199113078 |
0.612 |
|
| 2010 |
Mori K. Application of Biochemical Methods in Enantioselective Synthesis of Bioactive Natural Products Bulletin Des SociéTéS Chimiques Belges. 101: 393-405. DOI: 10.1002/Bscb.19921010505 |
0.377 |
|
| 2010 |
Mori K, Komatsu M. Synthesis and Absolute Configuration of Zonarol. A Fungitoxic Hydroquinone from the Brown Seaweed Dictyoptfris Zonarioides(1) Bulletin Des SociéTéS Chimiques Belges. 95: 771-781. DOI: 10.1002/Bscb.19860950906 |
0.402 |
|
| 2009 |
Kitazawa S, Kitazawa R, Kondo T, Mori K, Matsui T, Watanabe H, Watanabe M. Fatal cardiac tamponade due to coronary sinus thrombosis in acute lymphoblastic leukaemia: a case report. Cases Journal. 2: 9095. PMID 20062732 DOI: 10.1186/1757-1626-2-9095 |
0.471 |
|
| 2009 |
Hashimoto T, Tashiro T, Kitahara T, Mori K, Sasaki M, Takikawa H. First synthesis of (+/-)-basidifferquinone C, an inducer for fruiting-body formation in Polyporus arcularius. Bioscience, Biotechnology, and Biochemistry. 73: 2299-302. PMID 19809187 DOI: 10.1271/Bbb.90408 |
0.627 |
|
| 2009 |
Tashiro T, Nakagawa R, Hirokawa T, Inoue S, Watarai H, Taniguchi M, Mori K. RCAI-37, 56, 59, 60, 92, 101, and 102, cyclitol and carbasugar analogs of KRN7000: their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines. Bioorganic & Medicinal Chemistry. 17: 6360-73. PMID 19656685 DOI: 10.1016/J.Bmc.2009.07.025 |
0.335 |
|
| 2009 |
Okamura K, Watanabe T, Onishi T, Watanabe H, Fujii E, Mori K, Matsuda J. Successful allogeneic unrelated bone marrow transplantation using reduced-intensity conditioning for the treatment of X-linked adrenoleukodystrophy in a one-yr-old boy. Pediatric Transplantation. 13: 130-3. PMID 18822105 DOI: 10.1111/j.1399-3046.2008.00962.x |
0.476 |
|
| 2009 |
Mori K, Tashiro T. Synthesis of all the four stereoisomers of (1′S)-1-ethyl-2-methylpropyl 3,13-dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegata Tetrahedron Letters. 50: 3266-3269. DOI: 10.1016/J.Tetlet.2009.02.046 |
0.442 |
|
| 2008 |
Tashiro T, Osada K, Mori K. Syntheses of 2-Isopropyl-4,5-dihydrothiazole and 6-Hydroxy-6-methyl-3-heptanone, pheromone components of the male mouse, Mus musculus. Bioscience, Biotechnology, and Biochemistry. 72: 2398-402. PMID 18776685 DOI: 10.1271/Bbb.80293 |
0.33 |
|
| 2008 |
Koike H, Iijima M, Mori K, Yamamoto M, Hattori N, Watanabe H, Tanaka F, Doyu M, Sobue G. Neuropathic pain correlates with myelinated fibre loss and cytokine profile in POEMS syndrome. Journal of Neurology, Neurosurgery, and Psychiatry. 79: 1171-9. PMID 18356256 DOI: 10.1136/jnnp.2007.135681 |
0.479 |
|
| 2008 |
Fuhshuku K, Hongo N, Tashiro T, Masuda Y, Nakagawa R, Seino K, Taniguchi M, Mori K. RCAI-8, 9, 18, 19, and 49-52, conformationally restricted analogues of KRN7000 with an azetidine or a pyrrolidine ring: Their synthesis and bioactivity for mouse natural killer T cells to produce cytokines. Bioorganic & Medicinal Chemistry. 16: 950-64. PMID 17950609 DOI: 10.1016/J.Bmc.2007.10.008 |
0.308 |
|
| 2008 |
Tashiro T, Nakagawa R, Inoue S, Shiozaki M, Watarai H, Taniguchi M, Mori K. RCAI-61, the 6′-O-methylated analog of KRN7000: its synthesis and potent bioactivity for mouse lymphocytes to produce interferon-γ in vivo Tetrahedron Letters. 49: 6827-6830. DOI: 10.1016/J.Tetlet.2008.09.074 |
0.349 |
|
| 2008 |
Takikawa H, Hashimoto T, Matsuura M, Tashiro T, Kitahara T, Mori K, Sasaki M. Synthetic studies on basidifferquinones: the first synthesis of (±)-basidifferquinone C Tetrahedron Letters. 49: 2258-2261. DOI: 10.1016/J.Tetlet.2008.02.011 |
0.625 |
|
| 2008 |
Mori K, Tashiro T, Yoshimura T, Takita M, Tabata J, Hiradate S, Sugie H. Determination of the absolute configuration of the male aggregation pheromone, 2-methyl-6-(4′-methylenebicyclo[3.1.0]hexyl)hept-2-en-1-ol, of the stink bug Erysarcoris lewisi (Distant) as 2Z,6R,1′S,5′S by its synthesis Tetrahedron Letters. 49: 354-357. DOI: 10.1016/J.Tetlet.2007.11.036 |
0.424 |
|
| 2008 |
Tashiro T, Mori K. Synthesis and absolute configuration of the male aggregation pheromone of the stink bug Erysarcoris lewisi (Distant), (2Z,6R,1′S,5′S)-2-methyl-6-(4′-methylenebicyclo[3.1.0]hexyl)hept-2-en-1-ol Tetrahedron: Asymmetry. 19: 1215-1223. DOI: 10.1016/J.Tetasy.2008.04.029 |
0.416 |
|
| 2008 |
Kamata N, Esaki K, Mori K, Takemoto H, Mitsunaga T, Honda H. Field trap test for bioassay of synthetic (1S,4R)-4-isopropyl-1-methyl-2-cyclohexen-1-ol as an aggregation pheromone of Platypus quercivorus (Coleoptera: Platipodidae) Journal of Forest Research. 13: 122-126. DOI: 10.1007/S10310-007-0053-5 |
0.338 |
|
| 2007 |
Koike H, Iijima M, Mori K, Yamamoto M, Hattori N, Katsuno M, Tanaka F, Watanabe H, Doyu M, Yoshikawa H, Sobue G. Nonmyelinating Schwann cell involvement with well-preserved unmyelinated axons in Charcot-Marie-Tooth disease type 1A. Journal of Neuropathology and Experimental Neurology. 66: 1027-36. PMID 17984684 DOI: 10.1097/NEN.0b013e3181598294 |
0.474 |
|
| 2007 |
Watanabe H, Mori N, Itoh D, Kitahara T, Mori K. Synthetic study towards azadirachtin: an efficient and stereoselective construction of the AB rings with full functionality. Angewandte Chemie (International Ed. in English). 46: 1512-6. PMID 17226885 DOI: 10.1002/Anie.200604097 |
0.72 |
|
| 2007 |
Tashiro T, Nakagawa R, Hirokawa T, Inoue S, Watarai H, Taniguchi M, Mori K. RCAI-56, a carbocyclic analogue of KRN7000: its synthesis and potent activity for natural killer (NK) T cells to preferentially produce interferon-γ Tetrahedron Letters. 48: 3343-3347. DOI: 10.1016/J.Tetlet.2007.03.074 |
0.335 |
|
| 2007 |
Fuhshuku K, Mori K. Synthesis of two piperidine alkaloids, (−)-deoxoprosopinine and (−)-deoxoprosophylline, from 6-hydroxylated dihydrosphingosine derivatives Tetrahedron: Asymmetry. 18: 2104-2107. DOI: 10.1016/J.Tetasy.2007.08.028 |
0.42 |
|
| 2006 |
Koike H, Watanabe H, Inukai A, Iijima M, Mori K, Hattori N, Sobue G. Myopathy in thiamine deficiency: analysis of a case. Journal of the Neurological Sciences. 249: 175-9. PMID 16920153 DOI: 10.1016/j.jns.2006.06.016 |
0.472 |
|
| 2006 |
Sasajima T, Suzuki T, Mori K, Ichii O, Tai M, Ochiai H, Ejiri Y, Watanabe H, Ohira H, Obara K, Sato Y. A case of idiopathic portal hypertension associated with rheumatoid arthritis. Modern Rheumatology / the Japan Rheumatism Association. 16: 92-6. PMID 16633928 DOI: 10.1007/s10165-006-0456-8 |
0.479 |
|
| 2006 |
Morita M, Mori K, Tominaga K, Terajima J, Hirose K, Watanabe H, Izumiya H. Characterization of lysine decarboxylase-negative strains of Salmonella enterica serovar Enteritidis disseminated in Japan. Fems Immunology and Medical Microbiology. 46: 381-5. PMID 16553811 DOI: 10.1111/j.1574-695X.2006.00043.x |
0.487 |
|
| 2006 |
Masuda Y, Tashiro T, Mori K. Synthesis of (+)-carpamic acid from (+)-alanine Tetrahedron: Asymmetry. 17: 3380-3385. DOI: 10.1016/J.Tetasy.2006.12.025 |
0.442 |
|
| 2006 |
Yajima A, Mori K. Synthetic Microbiol Chemistry, XXIX!. Synthesis of Both the Enantiomers of Incrustoporin, an Antibiotic from Incrustoporia carneola Liebigs Annalen. 1996: 1091-1093. DOI: 10.1002/Jlac.199619960707 |
0.424 |
|
| 2006 |
Yajima A, Takikawa H, Mori K. Synthesis of Sphingosine Relatives, XVIII!. Synthesis of Penazetidine A, an Alkaloid Inhibitor of Protein Kinase C Isolated from the Marine Sponge Penares sollasi† Liebigs Annalen. 1996: 1083-1089. DOI: 10.1002/Jlac.199619960706 |
0.397 |
|
| 2006 |
Yajima A, Takikawa H, Mori K. Synthesis of Mono- and Sesquiterpenoids, XXV. Synthesis of (6R*,7R*)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the Racemate of the Antibacterial Sesquiterpene from Premna oligotricha, and Its (6R*,7S*) Isomer Liebigs Annalen. 1996: 891-897. DOI: 10.1002/Jlac.199619960606 |
0.424 |
|
| 2006 |
Mori K, Horikiri H. Pheromone Synthesis, CLXXIV. Synthesis of (5R,11S)-5,11-Dimethylheptadecane and (S)-2,5-Dimethylheptadecane, the Major and the Minor Components of the Sex Pheromone of the Geometrid Moth, Lambdina fiscellaria lugubrosa Liebigs Annalen. 1996: 501-505. DOI: 10.1002/Jlac.199619960409 |
0.45 |
|
| 2006 |
Mori K, Uenishi K. Synthesis of Sphingosine Relatives, XVII! Synthesis of (2S,2' R,3R,3' E,4E,8E)-1-O-(β-D-Glucopyranosyl)-N-(2'-hydroxy-3'-octadecenoyl)-9-methyl-4,8-sphingadienine (Pen II), the Major Cerebroside Isolated from Penicillium funiculosum as the Fruiting-Induce Liebigs Annalen. 1996: 1-6. DOI: 10.1002/Jlac.199619960102 |
0.368 |
|
| 2005 |
Tóth M, Csonka E, Bartelt RJ, Cossé AA, Zilkowski BW, Muto SE, Mori K. Pheromonal activity of compounds identified from male Phyllotreta cruciferae: field tests of racemic mixtures, pure enantiomers, and combinations with allyl isothiocyanate. Journal of Chemical Ecology. 31: 2705-20. PMID 16273436 DOI: 10.1007/S10886-005-7621-Y |
0.325 |
|
| 2005 |
Spiegel CN, Jeanbourquin P, Guerin PM, Hooper AM, Claude S, Tabacchi R, Sano S, Mori K. (1S,3S,7R)-3-methyl-alpha-himachalene from the male sandfly Lutzomyia longipalpis (Diptera: Psychodidae) induces neurophysiological responses and attracts both males and females. Journal of Insect Physiology. 51: 1366-75. PMID 16226273 DOI: 10.1016/J.Jinsphys.2005.08.007 |
0.338 |
|
| 2005 |
Izumiya H, Mori K, Kurazono T, Yamaguchi M, Higashide M, Konishi N, Kai A, Morita K, Terajima J, Watanabe H. Characterization of isolates of Salmonella enterica serovar typhimurium displaying high-level fluoroquinolone resistance in Japan. Journal of Clinical Microbiology. 43: 5074-9. PMID 16207965 DOI: 10.1128/JCM.43.10.5074-5079.2005 |
0.484 |
|
| 2005 |
Mori K, Iijima M, Koike H, Hattori N, Tanaka F, Watanabe H, Katsuno M, Fujita A, Aiba I, Ogata A, Saito T, Asakura K, Yoshida M, Hirayama M, Sobue G. The wide spectrum of clinical manifestations in Sjögren's syndrome-associated neuropathy. Brain : a Journal of Neurology. 128: 2518-34. PMID 16049042 DOI: 10.1093/brain/awh605 |
0.481 |
|
| 2005 |
Izumiya H, Mori K, Higashide M, Tamura K, Takai N, Hirose K, Terajima J, Watanabe H. Identification of CTX-M-14 {beta}-lactamase in a Salmonella enterica serovar enteritidis isolate from Japan. Antimicrobial Agents and Chemotherapy. 49: 2568-70. PMID 15917576 DOI: 10.1128/AAC.49.6.2568-2570.2005 |
0.496 |
|
| 2005 |
Tashiro T, Mori K. Enzyme-assisted synthesis of (S)-1,3-dihydroxy-3,7-dimethyl-6-octen-2-one, the male-produced aggregation pheromone of the Colorado potato beetle, and its (R)-enantiomer Tetrahedron: Asymmetry. 16: 1801-1806. DOI: 10.1016/J.Tetasy.2005.03.030 |
0.431 |
|
| 2005 |
Szöcs G, Tóth M, Mori K. Absolute configuration of the major sex pheromone component of the satin moth, Leucoma salicis, verified by field trapping test in Hungary Chemoecology. 15: 127-128. DOI: 10.1007/S00049-005-0293-9 |
0.317 |
|
| 2004 |
Mori K, Ohtaki T, Ohrui H, Berkebile DR, Carlson DA. Synthesis of the four stereoisomers of 7-acetoxy-15-methylnonacosane, a component of the female sex pheromone of the screwworm fly, Cochliomyia hominivorax. Bioscience, Biotechnology, and Biochemistry. 68: 1768-78. PMID 15322362 DOI: 10.1271/Bbb.68.1768 |
0.392 |
|
| 2004 |
Imamura Y, Takikawa H, Sasaki M, Mori K. Triterpenoid total synthesis. Synthesis and absolute configuration of mispyric acid. Organic & Biomolecular Chemistry. 2: 2236-44. PMID 15280961 DOI: 10.1039/B406820C |
0.406 |
|
| 2004 |
Tashiro T, Kurosawa S, Mori K. Revision of the structure of the major aggregation pheromone of the broad-horned flour beetle (Gnatocerus cornutus) to (1S,4R,5R)-alpha-acoradiene by its synthesis. Bioscience, Biotechnology, and Biochemistry. 68: 663-70. PMID 15056901 DOI: 10.1271/Bbb.68.663 |
0.379 |
|
| 2004 |
Ohzeki T, Mori K. Synthetic racemate and enantiomers of cytosporone E, a metabolite of an endophytic fungus, show indistinguishably weak antimicrobial activity. Bioscience, Biotechnology, and Biochemistry. 67: 2584-90. PMID 14730136 DOI: 10.1271/Bbb.67.2584 |
0.347 |
|
| 2004 |
Ohzeki T, Mori K. Synthesis and absolute configuration of (-)-3-butyl-7-hydroxyphthalide, a cytotoxic metabolite of Penicillium vulpinum. Bioscience, Biotechnology, and Biochemistry. 67: 2240-4. PMID 14586114 DOI: 10.1271/Bbb.67.2240 |
0.435 |
|
| 2004 |
Masuda Y, Fujita K, Mori K. Synthesis of (4R,6S,7R)-7-hydroxy-4,6-dimethyl-3-nonanone and (3R,5S,6R)- 6-hydroxy-3,5-dimethyl-2-octanone, the pheromone components of the bostrychid beetle, Dinoderus bifoveolatus. Bioscience, Biotechnology, and Biochemistry. 67: 1744-50. PMID 12951509 DOI: 10.1271/Bbb.67.1744 |
0.361 |
|
| 2004 |
Muto SE, Mori K. Synthesis of the four components of the female sex pheromone of the painted apple moth, Teia anartoides. Bioscience, Biotechnology, and Biochemistry. 67: 1559-67. PMID 12913301 DOI: 10.1271/Bbb.67.1559 |
0.333 |
|
| 2004 |
Mori K. Synthesis of Optically Active and Naturally Occurring Compounds of Biological Interests Journal of Synthetic Organic Chemistry, Japan. 62: 2-13. DOI: 10.5059/Yukigoseikyokaishi.62.2 |
0.427 |
|
| 2004 |
Mori K, Tashiro T. Useful Reactions in Modern Pheromone Synthesis Current Organic Synthesis. 1: 11-29. DOI: 10.2174/1570179043485466 |
0.372 |
|
| 2004 |
Yajima A, Mori K, Yabuta G. Total synthesis of ent-cassa-12,15-diene, a putative precursor of rice phytoalexins, phytocassanes A–E Tetrahedron Letters. 45: 167-169. DOI: 10.1016/J.Tetlet.2003.10.131 |
0.454 |
|
| 2004 |
Muto S, Bando M, Mori K. Synthesis and Stereochemistry of the Four Himachalene-Type Sesquiterpenes Isolated from the Flea Beetle (Aphthona flava) as Pheromone Candidates European Journal of Organic Chemistry. 2004: 1946-1952. DOI: 10.1002/Ejoc.200300812 |
0.386 |
|
| 2004 |
Mori K, Ohtaki T, Ohrui H, Berkebile DR, Carlson DA. Synthesis of the four stereoisomers of 6-acetoxy-19-methylnonacosane, the most potent component of the female sex pheromone of the new world screwworm fly, with special emphasis on partial racemization in the course of catalytic hydrogenation European Journal of Organic Chemistry. 1089-1096. DOI: 10.1002/Ejoc.200300669 |
0.33 |
|
| 2004 |
Shibata C, Mori K. Pheromone Synthesis. Part 223. Synthesis of (4R,9Z)-9-Octadecen-4-olide, the Female Sex Pheromone of Janus integer, and Its Enantiomer. Cheminform. 35. DOI: 10.1002/chin.200428218 |
0.322 |
|
| 2003 |
Mendel Z, Dunkelblum E, Branco M, Franco JC, Kurosawa S, Mori K. Synthesis and structure-activity relationship of diene modified analogs of Matsucoccus sex pheromones Naturwissenschaften. 90: 313-317. PMID 12883774 DOI: 10.1007/S00114-003-0429-0 |
0.312 |
|
| 2003 |
Ichihashi M, Mori K. Determination of the absolute configuration of (+)-xestoaminol C [(2S, 3R)-2-amino-3-tetradecanol], a metabolite of Fiji sponge, Xestospongia sp., by the synthesis of its N,O-diacetyl derivative. Bioscience, Biotechnology, and Biochemistry. 67: 329-33. PMID 12728994 DOI: 10.1271/Bbb.67.329 |
0.382 |
|
| 2003 |
Mori K, Bando M, Abe K. Determination of the stereochemistry of (-)-koninginin A by an X-ray analysis of its synthetic sample. Bioscience, Biotechnology, and Biochemistry. 66: 1779-81. PMID 12353648 DOI: 10.1271/Bbb.66.1779 |
0.33 |
|
| 2003 |
Masuda Y, Yoshida M, Mori K. Synthesis of (2S,2'R,3S,4R)-2-(2'-hydroxy-21'-methyidocosanoylamino)-1,3,4-pentadecanetriol, the ceramide sex pheromone of the female hair crab, Erimacrus isenbeckii. Bioscience, Biotechnology, and Biochemistry. 66: 1531-7. PMID 12224637 DOI: 10.1271/Bbb.66.1531 |
0.364 |
|
| 2003 |
Muto S, Mori K. Synthesis of all Four Stereoisomers of Leucomalure, Components of the Female Sex Pheromone of the Satin Moth, Leucoma salicis European Journal of Organic Chemistry. 2003: 1300-1307. DOI: 10.1002/Ejoc.200390186 |
0.391 |
|
| 2003 |
Tanada Y, Mori K. Synthesis and Absolute Configuration of (−)-Subersic Acid, a Sponge-Derived, Terpenoidal Inhibitor of Human 15-Lipoxygenase European Journal of Organic Chemistry. 2003: 848-854. DOI: 10.1002/Ejoc.200390128 |
0.393 |
|
| 2003 |
Tashiro T, Akasaka K, Ohrui H, Fattorusso E, Mori K. Synthesis of Sphingosine Relatives. Part 24. Determination of the Absolute Configuration at the Two Cyclopropane Moieties of Plakoside A, an Immunosuppressive Marine Galactosphingolipid. Cheminform. 34. DOI: 10.1002/chin.200311200 |
0.319 |
|
| 2003 |
Mori K, Mori H. Yeast Reduction of 2,2‐Dimethylcyclohexane‐1,3‐dione: (S)‐(+)‐3‐Hydroxy‐2,2‐dimethylcyclohexanone) Organic Syntheses. 56-56. DOI: 10.1002/0471264180.Os068.08 |
0.354 |
|
| 2002 |
Niwa K, Hamada H, Nakazawa M, Terai M, Tateno S, Sugimoto S, Watanabe H, Murakami A, Ohta M, Ishizawa A, Katoki T, Mori K, Yasui S, Kawahira Y, Akagi T, et al. Mortality and risk factors for late deaths in tetralogy of Fallot: the Japanese Nationwide Multicentric Survey. Cardiology in the Young. 12: 453-60. PMID 15773448 |
0.471 |
|
| 2002 |
Kikuchi S, Nakajima T, Kobayashi O, Yamazaki T, Kikuichi M, Mori K, Oura S, Watanabe H, Nagawa H, Otani R, Okamoto N, Kurosawa M, Anzai H, Konishi T, Futagawa S, et al. U-shaped effect of drinking and linear effect of smoking on risk for stomach cancer in Japan. Japanese Journal of Cancer Research : Gann. 93: 953-9. PMID 12359047 |
0.483 |
|
| 2002 |
Furukawa A, Shibata C, Mori K. Syntheses of four methyl-branched secondary acetates and a methyl-branched ketone as possible candidates for the female pheromone of the screwworm fly, Cochliomyia hominivorax. Bioscience, Biotechnology, and Biochemistry. 66: 1164-9. PMID 12092838 DOI: 10.1271/Bbb.66.1164 |
0.34 |
|
| 2002 |
Masuda Y, Mori K. Synthesis of the four stereoisomers of 3,12-dimethylheptacosane, (Z)-9-pentacosene and (Z)-9-heptacosene, the cuticular hydrocarbons of the ant, Diacamma sp.. Bioscience, Biotechnology, and Biochemistry. 66: 1032-8. PMID 12092812 DOI: 10.1271/Bbb.66.1032 |
0.338 |
|
| 2002 |
Kousaka T, Mori K. Synthesis of (1R,2S)-1-(3'-chloro-4' -methoxyphenyl)-1,2-propanediol (trametol) and (1R,2S)-1-(3',5'-dichloro-4'-methoxyphenyl)-1,2-propanediol, chlorinated fungal metabolites in the natural environment. Bioscience, Biotechnology, and Biochemistry. 66: 697-701. PMID 12005076 DOI: 10.1271/Bbb.66.697 |
0.407 |
|
| 2002 |
Shibata C, Furukawa A, Mori K. Syntheses of racemic and diastereomeric mixtures of 3,7,11,15-tetramethylhentriacontane and 4,8,12,16-tetramethyldotriacontane, the cuticular tetramethylalkanes of the tsetse fly, Glossina brevipalpis. Bioscience, Biotechnology, and Biochemistry. 66: 582-7. PMID 12005053 DOI: 10.1271/Bbb.66.582 |
0.366 |
|
| 2002 |
Marukawa K, Mori K. Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid MothEndoclita excrescens, and Its Enantiomer Chemistry Letters. 31: 40-41. DOI: 10.1246/Cl.2002.40 |
0.381 |
|
| 2002 |
Imamura Y, Takikawa H, Mori K. Synthesis of (±)-mispyric acid, a triterpene inhibitor of DNA polymerase β isolated from Mischocarpus pyriformis Tetrahedron Letters. 43: 5743-5746. DOI: 10.1016/S0040-4039(02)01193-0 |
0.315 |
|
| 2002 |
Tashiro T, Akasaka K, Ohrui H, Fattorusso E, Mori K. Determination of the Absolute Configuration at the Two Cyclopropane Moieties of Plakoside A, an Immunosuppressive Marine Galactosphingolipid European Journal of Organic Chemistry. 2002: 3659-3665. DOI: 10.1016/S0040-4039(02)00606-8 |
0.398 |
|
| 2002 |
Marukawa K, Mori K. Synthesis of (1R,3S,5S)‐1,3,8‐Trimethyl‐2,9‐dioxabicyclo[3.3.1]non‐7‐ene, the Male Pheromone of a Hepialid Moth, Endoclita excrescens, and Its Enantiomer European Journal of Organic Chemistry. 2002: 3974-3978. DOI: 10.1002/1099-0690(200212)2002:23<3974::Aid-Ejoc3974>3.0.Co;2-Z |
0.365 |
|
| 2001 |
Ichihashi M, Takikawa H, Mori K. Synthesis of (R)-(+)-Hippospongic Acid A, a Triterpene Isolated from the Marine Sponge, Hippospongia sp. Bioscience, Biotechnology, and Biochemistry. 65: 2569-2572. PMID 11791737 DOI: 10.1271/Bbb.65.2569 |
0.389 |
|
| 2001 |
Abe Y, Mori K. Simple synthesis of climacostol, a defensive secretion by the ciliate Climacostomum virens. Bioscience, Biotechnology, and Biochemistry. 65: 2110-2112. PMID 11676032 DOI: 10.1271/Bbb.65.2110 |
0.442 |
|
| 2001 |
Takagi M, Takikawa H, Mori K. Synthesis of methyl (5Z,9Z,17R)-17-methylnonadeca-5,9-dienoate, the (R)-enantiomer of the structure proposed for a metabolite of the Philippine sponge Plakinastrella sp. Bioscience, Biotechnology, and Biochemistry. 65: 2065-2069. PMID 11676022 DOI: 10.1271/Bbb.65.2065 |
0.381 |
|
| 2001 |
Lizarraga JR, Mori K. Synthesis of (+/-)-leucomalure [(3Z,6R*,7S*,9R*,10S*)-cis-6,7-cis-9,10-diepoxy-3-henicosene], the major components of the female sex pheromone of the satin moth. Natural Product Letters. 15: 89-92. PMID 11561450 DOI: 10.1080/10575630108041264 |
0.361 |
|
| 2001 |
Fujita K, Mori K. New Synthesis of Serricornin, the Female Sex Pheromone of the Cigarette Beetle Bioscience, Biotechnology, and Biochemistry. 65: 1429-1433. PMID 11471749 DOI: 10.1271/Bbb.65.1429 |
0.353 |
|
| 2001 |
Duff CM, Gries G, Mori K, Shirai Y, Seki M, Takikawa H, Sheng T, Slessor KN, Gries R, Maier CT, Ferguson DC. Does pheromone biology of Lambdina athasaria and L. pellucidaria contribute to their reproductive isolation? Journal of Chemical Ecology. 27: 431-42. PMID 11441437 DOI: 10.1023/A:1010324519127 |
0.352 |
|
| 2001 |
Nozawa D, Takikawa H, Mori K. Synthesis and absolute configuration of Stellettadine A: a marine alkaloid that induces larval metamorphosis in ascidians. Bioorganic & Medicinal Chemistry Letters. 11: 1481-1483. PMID 11412965 DOI: 10.1016/S0960-894X(01)00015-4 |
0.405 |
|
| 2001 |
Abe Y, Takikawa H, Mori K. Synthesis of gibbilimbols A-D, cytotoxic and antibacterial alkenylphenols isolated from Piper gibbilimbum. Bioscience, Biotechnology, and Biochemistry. 65: 732-735. PMID 11330702 DOI: 10.1271/Bbb.65.732 |
0.304 |
|
| 2001 |
Marukawa K, Takikawa H, Mori K. Synthesis of the enantiomers of some methyl-branched cuticular hydrocarbons of the Ant, Diacamma sp. Bioscience, Biotechnology, and Biochemistry. 65: 305-314. PMID 11302163 DOI: 10.1271/Bbb.65.305 |
0.373 |
|
| 2001 |
Ohzeki T, Mori K. Synthesis of Corollosporine, an Antibacterial Metabolite of the Marine Fungus Corollospora maritima Bioscience, Biotechnology, and Biochemistry. 65: 172-175. PMID 11272824 DOI: 10.1271/Bbb.65.172 |
0.345 |
|
| 2001 |
Tsujimori H, Mori K. Synthesis of the racemate of the stereoisomer at C-6a of BE-40644, a bioactive metabolite of Actinoplanes sp. with a sesquiterpene-substituted p-benzoquinone structure. Bioscience, Biotechnology, and Biochemistry. 65: 167-171. PMID 11272823 DOI: 10.1271/Bbb.65.167 |
0.343 |
|
| 2001 |
Mori K. Recent results in the synthesis of ecologically important bioregulators Pure and Applied Chemistry. 73: 601-606. DOI: 10.1351/pac200173030601 |
0.348 |
|
| 2001 |
Yoshida M, Takikawa H, Mori K. Triterpenoid total synthesis. Part 6. Synthesis of testudinariols A and B, triterpene metabolites of the marine mollusc Pleurobrancus testudinarius Journal of the Chemical Society-Perkin Transactions 1. 1007-1017. DOI: 10.1039/B100777G |
0.41 |
|
| 2001 |
Takikawa H, Nozawa D, Mori K. Synthesis and absolute configuration of stellettadine A, a bisguanidinium alkaloid isolated from a marine sponge Stelletta sp. Journal of the Chemical Society-Perkin Transactions 1. 657-661. DOI: 10.1039/B100206F |
0.382 |
|
| 2001 |
Seki M, Kayo A, Mori K. Synthesis of (2 S ,3 R ,11 S ,12 R ,2‴ R ,11‴ S ,12‴ R )-plakoside A, a prenylated and immunosuppressive marine galactosphingolipid with cyclopropane-containing alkyl chains Tetrahedron Letters. 42: 2357-2360. DOI: 10.1016/S0040-4039(01)00175-7 |
0.367 |
|
| 2001 |
Takikawa H, Yoshida M, Mori K. Synthesis of (+)-testudinariol A, a triterpene metabolite of the marine mollusc Pleurobrancus testudinarius Tetrahedron Letters. 42: 1527-1530. DOI: 10.1016/S0040-4039(00)02179-1 |
0.395 |
|
| 2001 |
Mori K. ChemInform Abstract: Chemoenzymatic Synthesis of Pheromones, Terpenes, and Other Bioregulators Cheminform. 32: no-no. DOI: 10.1002/chin.200109284 |
0.349 |
|
| 2001 |
Muto S, Mori K. Synthesis of Posticlure [(6Z,9Z,11S,12S)-11,12-Epoxyhenicosa-6,9-diene], the Female Sex Pheromone of Orgyia postica European Journal of Organic Chemistry. 2001: 4635. DOI: 10.1002/1099-0690(200112)2001:24<4635::Aid-Ejoc4635>3.0.Co;2-J |
0.424 |
|
| 2001 |
Kurosawa S, Bando M, Mori K. Synthesis of (1R,4R,5S)-(+)-Acoradiene, the Structure Proposed for the Aggregation Pheromone of the Broad-Horned Flour Beetle European Journal of Organic Chemistry. 2001: 4395-4399. DOI: 10.1002/1099-0690(200112)2001:23<4395::Aid-Ejoc4395>3.0.Co;2-Q |
0.38 |
|
| 2001 |
Tanada Y, Mori K. Synthesis and Absolute Configuration of Nocardione A and B, Furano-o-naphthoquinone-Type Metabolites of Nocardia sp. with Antifungal, Cytotoxic, and Enzyme Inhibitory Activities European Journal of Organic Chemistry. 2001: 4313. DOI: 10.1002/1099-0690(200111)2001:22<4313::Aid-Ejoc4313>3.0.Co;2-J |
0.393 |
|
| 2001 |
Seki M, Mori K. Synthesis of a Prenylated and Immunosuppressive Marine Galactosphingolipid with Cyclopropane-Containing Alkyl Chains: (2S,3R,11S,12R,2′′′R,5′′′Z,11′′′S,12′′′R)-Plakoside A and Its (2S,3R,11R,12S,2′′′R,5′′′Z,11′′′R,12′′′S) Isomer European Journal of Organic Chemistry. 2001: 3797-3809. DOI: 10.1002/1099-0690(200110)2001:20<3797::Aid-Ejoc3797>3.0.Co;2-Y |
0.383 |
|
| 2001 |
Kimura T, Carlson D, Mori K. Synthesis of All the Stereoisomers of 13,17-Dimethyl-1-tritriacontene and 13,17-Dimethyl-1-pentatriacontene, the Contact Sex Pheromone Components of the Female Tsetse Fly, Glossina austeni European Journal of Organic Chemistry. 2001: 3385. DOI: 10.1002/1099-0690(200109)2001:17<3385::Aid-Ejoc3385>3.0.Co;2-P |
0.378 |
|
| 2001 |
Okochi T, Mori K. New Enantioselective Synthesis of (10R,11S)-(+)-Juvenile Hormones I and II European Journal of Organic Chemistry. 2001: 2145-2150. DOI: 10.1002/1099-0690(200106)2001:11<2145::Aid-Ejoc2145>3.0.Co;2-J |
0.389 |
|
| 2001 |
Tanada Y, Mori K. Synthesis and Absolute Configuration of (−)-Neuchromenin, a Neurotrophic Metabolite ofEupenicillium javanicum var.meloforme, and Its Enantiomer European Journal of Organic Chemistry. 2001: 1963-1966. DOI: 10.1002/1099-0690(200105)2001:10<1963::Aid-Ejoc1963>3.0.Co;2-K |
0.39 |
|
| 2001 |
Seki M, Mori K. The Absolute Configuration of Axinellamine A, a Pyrrole Alkaloid of the Marine SpongeAxinella sp., was Determined asR by Synthesizing Its (S)-Isomer European Journal of Organic Chemistry. 2001: 503-506. DOI: 10.1002/1099-0690(200102)2001:3<503::Aid-Ejoc503>3.0.Co;2-6 |
0.412 |
|
| 2001 |
Fujita K, Mori K. Synthesis of (2R,4R)-Supellapyrone, the Sex Pheromone of the Brownbanded Cockroach,Supella longipalpa, and Its Three Stereoisomers European Journal of Organic Chemistry. 2001: 493-502. DOI: 10.1002/1099-0690(200102)2001:3<493::Aid-Ejoc493>3.0.Co;2-B |
0.403 |
|
| 2000 |
Nakamura Y, Mori K. New syntheses of the rice moth and stink bug pheromones by employing (2R, 6S)-7-acetoxy-2,6-dimethyl-1-heptanol as a building block. Bioscience, Biotechnology, and Biochemistry. 64: 1713-1721. PMID 10993161 DOI: 10.1271/Bbb.64.1713 |
0.348 |
|
| 2000 |
Kikuchi S, Nakajima T, Kobayashi O, Yamazaki T, Kikuichi M, Mori K, Oura S, Watanabe H, Nagawa H, Otani R, Okamoto N, Kurosawa M, Anzai H, Kubo T, Konishi T, et al. Effect of age on the relationship between gastric cancer and Helicobacter pylori. Tokyo Research Group of Prevention for Gastric Cancer. Japanese Journal of Cancer Research : Gann. 91: 774-9. PMID 10965016 |
0.48 |
|
| 2000 |
Tsujimori H, Mori K. Synthesis and absolute configuration of hongoquercin B, a sesquiterpene-substituted orsellinic acid isolated as a fungal metabolite. Bioscience, Biotechnology, and Biochemistry. 64: 1410-1415. PMID 10945257 DOI: 10.1271/Bbb.64.1410 |
0.385 |
|
| 2000 |
Mochizuki K, Takikawa H, Mori K. Synthesis of 2,2,4,4-tetramethyl-N,N'-bis(2,6-dimethylphenyl)cyclobutane-1,3-diimine , a unique compound from Arundo donax, and its analogues to test their antifeedant activity against the boll weevil, Anthonomus grandis. Bioscience, Biotechnology, and Biochemistry. 64: 647-651. PMID 10803974 DOI: 10.1271/Bbb.64.647 |
0.309 |
|
| 2000 |
Mori K. Organic synthesis and chemical ecology. Accounts of Chemical Research. 33: 102-110. PMID 10673318 DOI: 10.1021/Ar990006X |
0.417 |
|
| 2000 |
Takagi Y, Mori K. Enantioselective synthesis of (+)-polyzonimine, defensive monoterpene alkaloid produced by a milliped Polyzonium rosalbum, and determination of its S absolute configuration by Its conversion to (4S,5R,6S)-(+)-nitropolyzonamine Journal of the Brazilian Chemical Society. 11: 578-583. DOI: 10.1590/S0103-50532000000600005 |
0.303 |
|
| 2000 |
Tashiro T, Bando M, Mori K. Pheromone Synthesis, CCVIII: Synthesis of (1S,3S,7R)-3-Methyl-α-himachalene, the Sex Pheromone of the Sandfly Lutzomyia longipalpis from Jacobina, Brazil Synthesis. 2000: 1852-1862. DOI: 10.1055/S-2000-8220 |
0.451 |
|
| 2000 |
Nozawa D, Takikawa H, Mori K. Triterpenoid total synthesis. Part 5. Synthetic disproof of the triterpene structure proposed for naurol A, a cytotoxic metabolite of a Pacific sponge Journal of the Chemical Society-Perkin Transactions 1. 2043-2046. DOI: 10.1039/B002500N |
0.339 |
|
| 2000 |
Mori K, Takagi Y. Enantioselective synthesis of polyzonimine and nitropolyzonamine, spirocyclic compounds from the defensive glands of a millipede, Polyzonium rosalbum Tetrahedron Letters. 41: 6623-6625. DOI: 10.1016/S0040-4039(00)01133-3 |
0.44 |
|
| 2000 |
Mori K, Tashiro T, Sano S. Enantioselective synthesis of (1S,3S,7R)-3-methyl-α-himachalene, the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil Tetrahedron Letters. 41: 5243-5247. DOI: 10.1016/S0040-4039(00)00831-5 |
0.414 |
|
| 2000 |
Domon K, Mori K. Short Synthesis of Vesperal [(S)-10-Oxoisopiperitenone], the Female Sex Pheromone of the Longhorn Beetle (Vesperus xatarti), and of Its Enantiomer European Journal of Organic Chemistry. 2000: 3783-3785. DOI: 10.1002/1099-0690(200011)2000:22<3783::Aid-Ejoc3783>3.0.Co;2-O |
0.418 |
|
| 2000 |
Nakamura Y, Mori K. Synthesis of the Enantiomers ofanti-2,6-Dimethylheptane-1,7-diol Monotetrahydropyranyl Ether and Their Conversion into the Enantiomers of the Sex Pheromone Components of the Apple Leafminer,Lyonetia prunifoliella European Journal of Organic Chemistry. 2000: 2745-2753. DOI: 10.1002/1099-0690(200008)2000:15<2745::Aid-Ejoc2745>3.0.Co;2-I |
0.415 |
|
| 2000 |
Yoshida M, Mori K. Synthesis of Diospyrin, a Potential Agent Against Leishmaniasis and Related Parasitic Protozoan Diseases European Journal of Organic Chemistry. 2000: 1313-1317. DOI: 10.1002/1099-0690(200004)2000:7<1313::Aid-Ejoc1313>3.0.Co;2-I |
0.4 |
|
| 2000 |
Nakamura Y, Mori K. Synthesis of (3S,7S)- and (3S,7S,15S)- Stereoisomers of 3,7-Dimethyl-2-heptacosanone and 3,7,15-Trimethyl-2-heptacosanone, the Ketones Identified from the LocustSchistocerca gregaria European Journal of Organic Chemistry. 2000: 1307-1312. DOI: 10.1002/1099-0690(200004)2000:7<1307::Aid-Ejoc1307>3.0.Co;2-X |
0.35 |
|
| 2000 |
Kurosawa S, Mori K. Synthesis of (S)-9-Methylgermacrene-B, the Male-Produced Sex Pheromone of the SandflyLutzomyia longipalpis from Lapinha, Brazil, and Its (R)-Isomer European Journal of Organic Chemistry. 2000: 955-962. DOI: 10.1002/(Sici)1099-0690(200003)2000:6<955::Aid-Ejoc955>3.0.Co;2-Y |
0.404 |
|
| 2000 |
Tsujimori H, Bando M, Mori K. Synthesis and Absolute Configuration of Hongoquercin A, an Antibacterial Sesquiterpene-Substituted Orsellinic Acid Isolated as a Fungal Metabolite European Journal of Organic Chemistry. 2000: 297-302. DOI: 10.1002/(Sici)1099-0690(200001)2000:2<297::Aid-Ejoc297>3.0.Co;2-B |
0.361 |
|
| 1999 |
Takikawa H, Yoshida M, Mori K. Synthesis of 2-(4-Hydroxyphenyl)naphthalene-1,8-dicarboxylic Anhydride, a Phytoalexin Isolated from Unripe Banana (Musa acuminata). Bioscience, Biotechnology, and Biochemistry. 63: 1834-1836. PMID 26300176 DOI: 10.1271/Bbb.63.1834 |
0.349 |
|
| 1999 |
Horiuchi S, Takikawa H, Mori K. Enzymatic resolution of (±)-γ-cyclohomogeraniol and conversion of its (S)-Isomer to (S)-γ-coronal, the ambergris odorant Bioorganic & Medicinal Chemistry. 7: 723-726. PMID 10400325 DOI: 10.1016/S0968-0896(98)00209-0 |
0.362 |
|
| 1999 |
Shima J, Hino A, Yamada-Iyo C, Suzuki Y, Nakajima R, Watanabe H, Mori K, Takano H. Stress tolerance in doughs of Saccharomyces cerevisiae trehalase mutants derived from commercial Baker's yeast. Applied and Environmental Microbiology. 65: 2841-6. PMID 10388673 |
0.484 |
|
| 1999 |
Hamilton JGC, Hooper AM, Ibbotson HC, Kurosawa S, Mori K, Muto SE, Pickett JA. 9-Methylgermacrene-B is confirmed as the sex pheromone of the sandfly Lutzomyia longipalpis from Lapinha, Brazil, and the absolute stereochemistry defined as S Chemical Communications. 2335-2336. DOI: 10.1039/A907910F |
0.311 |
|
| 1999 |
Takikawa H, Nozawa D, Kayo A, Muto S, Mori K. Synthesis of sphingosine relatives. Part 22. Synthesis of sulfobacin A, B and flavocristamide A, new sulfonolipids isolated from Chryseobacterium sp. Journal of the Chemical Society-Perkin Transactions 1. 2467-2477. DOI: 10.1039/A904258J |
0.338 |
|
| 1999 |
Takikawa H, Koizumi J, Kato Y, Mori K. Triterpenoid total synthesis. Part 4.1 Synthesis of (±)-hippospongic acid A, a triterpene isolated from the marine sponge Hippospongia sp. Journal of the Chemical Society-Perkin Transactions 1. 2271-2275. DOI: 10.1039/A903870A |
0.37 |
|
| 1999 |
Hamilton JGC, Hooper AM, Pickett JA, Mori K, Sano S. 3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil Chemical Communications. 355-356. DOI: 10.1039/A900242A |
0.41 |
|
| 1999 |
Shirai Y, Seki M, Mori K. Synthesis of All the Stereoisomers of 7-Methylheptadecane and 7,11-Dimethylheptadecane, the Female Sex Pheromone Components of the Spring Hemlock Looper and the Pitch Pine Looper European Journal of Organic Chemistry. 1999: 3139-3145. DOI: 10.1002/(Sici)1099-0690(199911)1999:11<3139::Aid-Ejoc3139>3.0.Co;2-8 |
0.453 |
|
| 1999 |
Seki M, Mori K. Synthesis of (–)-Cytoxazone, a Novel Cytokine Modulator Isolated fromStreptomyces sp. European Journal of Organic Chemistry. 1999: 2965-2967. DOI: 10.1002/(Sici)1099-0690(199911)1999:11<2965::Aid-Ejoc2965>3.0.Co;2-H |
0.406 |
|
| 1999 |
Hirayama K, Mori K. Synthesis of (+)-Strigol and (+)-Orobanchol, the Germination Stimulants, and Their Stereoisomers by Employing Lipase-Catalyzed Asymmetric Acetylationas the Key Step European Journal of Organic Chemistry. 1999: 2211-2217. DOI: 10.1002/(Sici)1099-0690(199909)1999:9<2211::Aid-Ejoc2211>3.0.Co;2-O |
0.394 |
|
| 1999 |
Matsui J, Bando M, Kido M, Takeuchi Y, Mori K. Syntheses of (±)- and (+)-Sorgolactone, the Germination Stimulant fromSorghum bicolor European Journal of Organic Chemistry. 1999: 2183-2194. DOI: 10.1002/(Sici)1099-0690(199909)1999:9<2183::Aid-Ejoc2183>3.0.Co;2-4 |
0.322 |
|
| 1999 |
Nakamura Y, Mori K. Synthesis of (1S,2S,6S,10R)- and (1S,2R,6R,10R)-1,2,6,10-Tetramethyldodecyl Propanoate, the Components of the Sex Pheromone of the Pine Sawfly,Microdiprion pallipes European Journal of Organic Chemistry. 1999: 2175-2182. DOI: 10.1002/(Sici)1099-0690(199909)1999:9<2175::Aid-Ejoc2175>3.0.Co;2-V |
0.378 |
|
| 1999 |
Tashiro T, Mori K. Synthesis of the Enantiomers of 2-sec-Butyl-4,5-dihydrothiazole and (1R,5S,7R)-3,4-Dehydro-exo-brevicomin, Pheromone Components of the Male Mouse,Mus musculus European Journal of Organic Chemistry. 1999: 2167-2173. DOI: 10.1002/(Sici)1099-0690(199909)1999:9<2167::Aid-Ejoc2167>3.0.Co;2-L |
0.4 |
|
| 1999 |
Muto S, Nishimura Y, Mori K. Synthesis of Germacrene-B and Its Extension to the Synthesis of (±)-9-Methylgermacrene-B, the Racemate of the Male-Produced Sex Pheromone of the SandflyLutzomyia longipalpis from Lapinha, Brazil European Journal of Organic Chemistry. 1999: 2159-2165. DOI: 10.1002/(Sici)1099-0690(199909)1999:9<2159::Aid-Ejoc2159>3.0.Co;2-B |
0.302 |
|
| 1999 |
Otaka K, Mori K. Synthesis of Sphingofungin D and Its Three Diastereomers European Journal of Organic Chemistry. 1999: 1795-1802. DOI: 10.1002/(Sici)1099-0690(199908)1999:8<1795::Aid-Ejoc1795>3.0.Co;2-Y |
0.354 |
|
| 1999 |
Sano S, Mori K. Synthesis of (1R*,3R*,7R*)-3-Methyl-α-himachalene, the Racemate of the Male-Produced Sex Pheromone of the SandflyLutzomyia longipalpis from Jacobina, Brazil European Journal of Organic Chemistry. 1999: 1679-1686. DOI: 10.1002/(Sici)1099-0690(199907)1999:7<1679::Aid-Ejoc1679>3.0.Co;2-O |
0.399 |
|
| 1999 |
Domon K, Takikawa H, Mori K. Synthesis of the Enantiomers of (Z)-21-Methyl-8-pentatriacontene, the Major Component of the Female-Produced Contact Sex Pheromone of the Yellow-Spotted Longicorn Beetle,Psacothea hilaris European Journal of Organic Chemistry. 1999: 981-984. DOI: 10.1002/(Sici)1099-0690(199905)1999:5<981::Aid-Ejoc981>3.0.Co;2-3 |
0.353 |
|
| 1999 |
Domon K, Mori K. Simple Synthesis of (±)-Stigmolone (8-Hydroxy-2,5,8-trimethyl-4-nonanone), the Pheromone ofStigmatella aurantiaca European Journal of Organic Chemistry. 1999: 979-980. DOI: 10.1002/(Sici)1099-0690(199905)1999:5<979::Aid-Ejoc979>3.0.Co;2-C |
0.365 |
|
| 1999 |
Tamagawa H, Takikawa H, Mori K. Synthesis of All the Stereoisomers of 10,14-Dimethyloctadec-1-ene, 5,9-Dimethyloctadecane and 5,9-Dimethylheptadecane, the Sex Pheromone Components of the Apple Leafminer,Lyonetiaprunifoliella European Journal of Organic Chemistry. 1999: 973-978. DOI: 10.1002/(Sici)1099-0690(199905)1999:5<973::Aid-Ejoc973>3.0.Co;2-# |
0.399 |
|
| 1998 |
Matsushima Y, Kitahara T, Mori K. Lipase-catalyzed Kinetic Resolution of (±)-cis,cis-Spiro[4.4]nonane-1,6-diol. Bioscience, Biotechnology, and Biochemistry. 62: 1435-7. PMID 27397005 DOI: 10.1271/Bbb.62.1435 |
0.603 |
|
| 1998 |
Mori K, Audran G, Monti H. The First Synthesis of Coniochaetones A and (±)-B: Two Benzopyranone Derivatives Synlett. 9: 259-260. DOI: 10.1055/S-1998-1628 |
0.318 |
|
| 1998 |
Takanashi S, Takagi M, Takikawa H, Mori K. Synthesis of elenic acid, an inhibitor of topoisomerase II from the sponge Plakinastrella sp. Journal of the Chemical Society-Perkin Transactions 1. 1603-1606. DOI: 10.1039/A801122B |
0.37 |
|
| 1998 |
Takikawa H, Muto S, Mori K. Diastereoselective epoxidation of the double bond at C-4 of sphingosines to provide phytosphingosine relatives such as α-galactosylceramide KRN7000 Tetrahedron. 54: 3141-3150. DOI: 10.1016/S0040-4020(98)00065-9 |
0.31 |
|
| 1998 |
Mori K. Chirality And Insect Pheromones Chirality. 10: 578-586. DOI: 10.1002/(Sici)1520-636X(1998)10:7<578::Aid-Chir5>3.0.Co;2-Z |
0.419 |
|
| 1998 |
Horiuchi S, Takikawa H, Mori K. Synthesis of (6S,7S)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the Opposite Enantiomer of the Antibacterial Sesquiterpene fromPremnaoligotricha, and the (R) Enantiomer of Ancistrodial, the Defensive Sesquiterpene fromAncistrotermes cavithorax European Journal of Organic Chemistry. 1998: 2851-2854. DOI: 10.1002/(Sici)1099-0690(199812)1998:12<2851::Aid-Ejoc2851>3.0.Co;2-E |
0.409 |
|
| 1998 |
Mori K, Takenaka M. Synthesis of the Enantiomers of 8-Hydroxy-2,5,8-trimethyl-4-nonanone, the Myxobacterial Pheromone ofStigmatella aurantiaca to Induce the Formation of Its Fruiting Body European Journal of Organic Chemistry. 1998: 2181-2184. DOI: 10.1002/(Sici)1099-0690(199810)1998:10<2181::Aid-Ejoc2181>3.0.Co;2-H |
0.364 |
|
| 1998 |
Mori K. Semiochemicals – Synthesis, Stereochemistry, and Bioactivity European Journal of Organic Chemistry. 1998: 1479-1489. DOI: 10.1002/(Sici)1099-0690(199808)1998:8<1479::Aid-Ejoc1479>3.0.Co;2-# |
0.308 |
|
| 1998 |
Mori K, Sano S, Yokoyama Y, Bando M, Kido M. Synthesis of Stegobiol and Its Oxidation to Stegobinone, the Components of the Female-Produced Sex Pheromone of the Drugstore Beetle European Journal of Organic Chemistry. 1998: 1135-1141. DOI: 10.1002/(Sici)1099-0690(199806)1998:6<1135::Aid-Ejoc1135>3.0.Co;2-K |
0.428 |
|
| 1998 |
Nishimura Y, Mori K. A New Synthesis of (−)-Frontalin, the Bark Beetle Pheromone European Journal of Organic Chemistry. 1998: 233-236. DOI: 10.1002/(Sici)1099-0690(199802)1998:2<233::Aid-Ejoc233>3.0.Co;2-M |
0.442 |
|
| 1998 |
Takikawa H, Yamazaki Y, Mori K. Synthesis and Absolute Configuration of Rotundial, a Mosquito Repellent from the Leaves ofVitex rotundiforia European Journal of Organic Chemistry. 1998: 229-232. DOI: 10.1002/(Sici)1099-0690(199802)1998:2<229::Aid-Ejoc229>3.0.Co;2-2 |
0.409 |
|
| 1998 |
Takanashi S, Mori K. Synthesis of the Analogues of Lurlenic Acid with Modification in the Side-Chain or in the Aromatic Nucleus: Summary of the Structure−Activity Relationships European Journal of Organic Chemistry. 1998: 43-55. DOI: 10.1002/(Sici)1099-0690(199801)1998:1<43::Aid-Ejoc43>3.0.Co;2-L |
0.394 |
|
| 1997 |
Uchida K, Watanabe H, Mori K. Synthesis of (±)-Hiburipyranone, a Cytotoxic Metabolite of Marine SpongeMycale adhaerens Bioscience, Biotechnology, and Biochemistry. 61: 1564-1567. DOI: 10.1271/Bbb.61.1564 |
0.615 |
|
| 1997 |
Watanabe H, Watanabe T, Kitahara T, Mori K. Concise Synthesis of a Racemic and Diastereomeric Mixture of the Sex Pheromones ofMatsucoccusPine Scales Bioscience, Biotechnology, and Biochemistry. 61: 127-130. DOI: 10.1271/Bbb.61.127 |
0.756 |
|
| 1997 |
Mori K. Pheromones: synthesis and bioactivity Chemical Communications. 1153-1158. DOI: 10.1039/A606625I |
0.463 |
|
| 1997 |
Takikawa H, Maeda T, Seki M, Koshino H, Mori K. Synthesis of sphingosine relatives. Part 19.1 Synthesis ofpenaresidin A and B, azetidine alkaloids with actomyosinATPase-activating properties Journal of the Chemical Society-Perkin Transactions 1. 97-112. DOI: 10.1039/A604276G |
0.383 |
|
| 1997 |
Mori K, Matsui J. Synthesis of (3aR,8S,8bS,2′R)-(+)-sorgolactone and its stereoisomers, the germination stimulant from sorghum bicolor Tetrahedron Letters. 38: 7891-7892. DOI: 10.1016/S0040-4039(97)10078-8 |
0.349 |
|
| 1997 |
Watanabe H, Onoda T, Kitahara T, Mori K. Synthesis of (+)-sorokinianin Tetrahedron Letters. 38: 6015-6018. DOI: 10.1016/S0040-4039(97)01337-3 |
0.765 |
|
| 1997 |
Watanabe H, Watanabe T, Mori K, Kitahara T. Synthetic study on azadirachtin (part 2). Construction of the decalin moiety with full functionality on B-ring Tetrahedron Letters. 38: 4429-4432. DOI: 10.1016/S0040-4039(97)00923-4 |
0.745 |
|
| 1997 |
Mori K, Audran G, Nakahara Y, Bando M, Kido M. Synthesis and absolute configuration of phyllanthurinolactone, the leaf-closing factor of a nyctinastic plant, Phyllanthus urinaria L. Tetrahedron Letters. 38: 575-578. DOI: 10.1016/S0040-4039(96)02375-1 |
0.324 |
|
| 1997 |
Takikawa H, Sano S, Mori K. Pheromone Synthesis, CLXXXVI. Synthesis of (1S,2R,5R)-Bicolorin, the Aggregation Pheromone of Male Beech Bark Beetles (Taphrorychus bicolor), and Its (1R,2R,5S) Isomer Liebigs Annalen. 1997: 2495-2498. DOI: 10.1002/Jlac.199719971211 |
0.401 |
|
| 1997 |
Takanashi S, Mori K. Pheromone Synthesis, CLXXXV Synthesis of the Analogues of Lurlenic Acid with a Modified Sugar Part:Chlamydomonas responds only to theD-xyloside Liebigs Annalen. 1997: 1081-1084. DOI: 10.1002/Jlac.199719970606 |
0.333 |
|
| 1997 |
Nakayama T, Mori K. Pheromone Synthesis, CLXXXIV. Synthesis and Absolute Configuration of Sordidin, the Male‐Produced Aggregation Pheromone of the Banana Weevil, cosmopolites sordidus Liebigs Annalen. 1997: 1075-1080. DOI: 10.1002/Jlac.199719970605 |
0.446 |
|
| 1997 |
Yokoyama Y, Mori K. Pheromone Synthesis, CLXXXII. Synthesis of (1R,1′R,5′R,7′R)- and (1S,1′R,5′R,7′R)- 1-hydroxy-exo-Brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle,dendroctonus ponderosae Liebigs Annalen. 1997: 845-849. DOI: 10.1002/Jlac.199719970509 |
0.47 |
|
| 1997 |
Nakayama T, Mori K. Pheromone Synthesis, CLXXXI. Synthesis of the Racemate and the Enantiomers of (Z)-7,15-Hexadecadien-4-olide, the Sex Pheromone of the Yellowish Elongate Chafer,Heptophylla picea Liebigs Annalen. 1997: 839-843. DOI: 10.1002/Jlac.199719970508 |
0.432 |
|
| 1997 |
Takanashi S, Mori K. Pheromone Synthesis, CLXXIX. Synthesis of Lurlenic Acid and Lurlenol, the Sex Pheromones of the Green FlagellateChlamydomonas Liebigs Annalen. 1997: 825-838. DOI: 10.1002/Jlac.199719970507 |
0.388 |
|
| 1997 |
Takikawa H, Shimbo K, Mori K. Pheromone Synthesis, Clxxxiii : Synthesis Of (1R,2R,5S,7R)- And (1R,2S,5S,7R)-2-Hydroxy-Exo-Brevicomin, The Components Of The Male-Produced Volatiles Of The Mountain Pine Beetle, Dendroctonus Ponderosae Liebigs Annalen. 1997: 821-824. DOI: 10.1002/Jlac.199719970506 |
0.399 |
|
| 1997 |
Takikawa H, Fujita K, Mori K. Pheromone Synthesis, CLXXX. Synthesis of (3S,11S)‐3,11‐Dimethyl‐2‐heptacosannone, a New Component of the Female Sex Pheromone of the German Cockroach Liebigs Annalen. 1997: 815-820. DOI: 10.1002/Jlac.199719970505 |
0.399 |
|
| 1997 |
Nomoto S, Mori K. Synthetic Microbial Chemistry, XXX. Synthesis of Acetophthalidin, a Fungal Metabolite which Inhibits the Progression of the Mammalian Cell Cycle Liebigs Annalen. 1997: 721-723. DOI: 10.1002/Jlac.199719970412 |
0.352 |
|
| 1997 |
Mori K, Takikawa H, Nishimura Y, Horikiri H. Pheromone Synthesis, CLXXVIII. – Synthesis of (−)‐exo‐Isobrevicomin and Its (−)‐endo Isomer, the Components of The Male‐Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae Liebigs Annalen. 1997: 327-332. DOI: 10.1002/Jlac.199719970209 |
0.448 |
|
| 1997 |
Takikawa H, Takenaka M, Mori K. Pheromone Synthesis, CLXXV.– Synthesis of Koiganal I and II, the Sex Pheromone Components of the Webbing Clothes Moth Liebigs Annalen. 1997: 139-140. DOI: 10.1002/Jlac.199719970120 |
0.335 |
|
| 1996 |
Yokoyama Y, Takikawa H, Mori K. Enzymatic preparation of (4R,6R)-4-hydroxy-1,7-dioxaspiro[5.5]undecane and its antipode, the minor component of the olive fruit fly pheromone. Bioorganic & Medicinal Chemistry. 4: 409-412. PMID 8733619 DOI: 10.1016/0968-0896(96)00017-X |
0.353 |
|
| 1996 |
Otsuka J, Watanabe H, Mori KT. Evolution of transcriptional regulation system through promiscuous coupling of regulatory proteins with operons; suggestion from protein sequence similarities in Escherichia coli. Journal of Theoretical Biology. 178: 183-204. PMID 8729576 DOI: 10.1006/jtbi.1996.0016 |
0.49 |
|
| 1996 |
Mori K. Recent results in pheromone synthesis Pure and Applied Chemistry. 68: 2111-2118. DOI: 10.1351/pac199668112111 |
0.306 |
|
| 1996 |
Mori K. Molecular Asymmetry and Pheromone Science Bioscience, Biotechnology, and Biochemistry. 60: 1925-1932. DOI: 10.1271/Bbb.60.1925 |
0.303 |
|
| 1996 |
Kobayashi J, Tsuda M, Cheng J, Ishibashi M, Takikawa H, Mori K. Absolute stereochemistry of penaresidins A and B Tetrahedron Letters. 37: 6775-6776. DOI: 10.1016/S0040-4039(96)01465-7 |
0.345 |
|
| 1996 |
Mori K, Nakayama T, Takikawa H. Synthesis and absolute configuration of sordidin, the male-produced aggregation pheromone of the banana weevil, Cosmopolites sordidus Tetrahedron Letters. 37: 3741-3744. DOI: 10.1016/0040-4039(96)00674-0 |
0.415 |
|
| 1996 |
Mori K, Takanashi S. Synthesis of lurlene, the sex pheromone of the green flagellate Chlamydomonas allensworthii Tetrahedron Letters. 37: 1821-1824. DOI: 10.1016/0040-4039(96)00127-X |
0.377 |
|
| 1996 |
Watanabe H, Watanabe T, Mori K. Enantioselective synthesis of the tricyclic furan moiety of azadirachtin, a potent insect antifeedant Tetrahedron. 52: 13939-13950. DOI: 10.1016/0040-4020(96)00856-3 |
0.671 |
|
| 1996 |
Takikawa H, Shirai Y, Kobayashi M, Mori K. Pheromone Synthesis, CLXXVI. Synthesis of the Four Stereoisomers of 3,13‐Dimethylheptadecane, the Major Sex Pheromone Component of the Western False Hemlock Looper Liebigs Annalen. 1996: 1965-1970. DOI: 10.1002/Jlac.199619961205 |
0.361 |
|
| 1996 |
Takenaka M, Takikawa H, Mori K. Pheromone Synthesis, CLXXVII. Synthesis of the Enantiomers of 2‐Methyl‐4‐heptanol and 2‐Methyl‐4‐octanol, the Pheromone Components of the West Indian Sugarcane Borer Liebigs Annalen. 1996: 1963-1964. DOI: 10.1002/Jlac.199619961204 |
0.412 |
|
| 1996 |
Mori K. Synthesis of heterocyclic bioregulators and semiochemicals Journal of Heterocyclic Chemistry. 33: 1497-1517. DOI: 10.1002/jhet.5570330507 |
0.341 |
|
| 1995 |
Nishio H, Mori K. Synthesis of the Esterified Cerebroside in the Epidermis of Guinea Pigs Bioscience, Biotechnology, and Biochemistry. 59: 1644-1647. PMID 8520109 DOI: 10.1271/Bbb.59.1644 |
0.34 |
|
| 1995 |
Kitahara T, Aono S, Mori K. Synthesis of both the enantiomers of aseanostatin P5 (sarcinic acid), an inhibitor of myeloperoxidase release, and four diastereomers of aggreceride A, a platelet aggregation inhibitor. Bioscience, Biotechnology, and Biochemistry. 59: 78-82. PMID 7765980 DOI: 10.1271/Bbb.59.78 |
0.616 |
|
| 1995 |
Mori K. Enantioselective Synthesis in Natural Products Chemistry Journal of Synthetic Organic Chemistry Japan. 53: 952-962. DOI: 10.5059/Yukigoseikyokaishi.53.952 |
0.386 |
|
| 1995 |
Tamura H, Sakakibara H, Yanai T, Takagi Y, Kitahara T, Mori K. Synthesis of Both the Enantiomers oftrans-Chrysanthenol andtrans-Chrysanthenyl Acetate as the Characteristic Major Constituents of Kougiku Bioscience, Biotechnology, and Biochemistry. 59: 1985-1986. DOI: 10.1271/Bbb.59.1985 |
0.669 |
|
| 1995 |
Awano K, Yanai T, Watanabe I, Takagi Y, Kitahara T, Mori K. Synthesis of All Four Possible Stereoisomers of 1-Phenyl-2,3-butanediol and Both Enantiomers of 3-Hydroxy-4-phenyl-2-butanone to Determine the Absolute Configuration of the Natural Constituents Bioscience, Biotechnology, and Biochemistry. 59: 1251-1254. DOI: 10.1271/Bbb.59.1251 |
0.691 |
|
| 1995 |
Khlebnikov V, Mori K, Terashima K, Tanaka Y, Sato M. Lipase-Catalyzed Resolution of Sterically Crowded 1,2-Diols. Chemical & Pharmaceutical Bulletin. 43: 1659-1662. DOI: 10.1248/Cpb.43.1659 |
0.314 |
|
| 1995 |
Mori K, Takeuchi Y. Synthesis of (2R*, 4R*)-supellapyrone, The Sex Pheromone of the Brownbanded Cockroach Natural Product Letters. 5: 275-280. DOI: 10.1080/10575639508044072 |
0.386 |
|
| 1995 |
Kinoshita Y, Watanabe H, Kitahara T, Mori K. Concise Construction of N-Alkylated Phenazinone Skeletons: Synthesis of Lavanducyanin (WS-9659A) Synlett. 1995: 186-188. DOI: 10.1055/S-1995-4905 |
0.726 |
|
| 1995 |
Mori K, Matsushima Y. Synthesis of Mono- and Sesquiterpenoids; XXIV: (-)-Homogynolide A, an Insect Antifeedant Isolated from Homogyne alpina Synthesis. 1995: 845-850. DOI: 10.1055/S-1995-4004 |
0.38 |
|
| 1995 |
Takikawa H, Maeda T, Mori K. Synthesis of penaresidin a, an azetidine alkaloid with actomyosin ATPase-activating property Tetrahedron Letters. 36: 7689-7692. DOI: 10.1016/0040-4039(95)01613-M |
0.372 |
|
| 1995 |
Mori K, Furuuchi T, Matsuyama K. Pheromone synthesis, CLXXI. A new synthesis of (2E,4E,6R10R)‐4,6,10,12‐tetramethyl‐2,4‐tridecadien‐7‐one (matsuone), the primary component of the sex pheromone of three Matsucoccus pine bast scales Liebigs Annalen. 1995: 2093-2099. DOI: 10.1002/Jlac.1995199512295 |
0.393 |
|
| 1995 |
Mori K, Murata N. Pheromone synthesis, CLXX. A new synthesis of faranal [(3S,4R,6E,10Z)‐3,4,7,11‐tetramethyl‐6,10‐tridecadienal], the trail pheromone of the pharaoh's ant, Monomorium pharaonis Liebigs Annalen. 1995: 2089-2092. DOI: 10.1002/Jlac.1995199512294 |
0.445 |
|
| 1995 |
Mori K, Koga Y. Diterpenoid total synthesis, XXXI. Synthesis and absolute configuration of (−)-stypoldione, a metabolite ofStypopodium zonale Liebigs Annalen. 1995: 1755-1763. DOI: 10.1002/Jlac.1995199510246 |
0.418 |
|
| 1995 |
Amaike M, Mori K. Pheromone synthesis CLXIX. Improved synthesis of the racemate of the hemiacetal pheromone of the spined citrus bug Biprorulus bibax Liebigs Annalen. 1995: 1451-1454. DOI: 10.1002/Jlac.1995199508197 |
0.419 |
|
| 1995 |
Mori K, Abe K. Synthetic microbial chemistry, XXVIII. Synthesis and absolute configuration of (−)-koninginin A Liebigs Annalen. 1995: 943-948. DOI: 10.1002/Jlac.1995199506135 |
0.446 |
|
| 1995 |
Mori K, Murata N. Pheromone Synthesis. Clxviii: Synthesis Of Cruentol (4S,5S)-5-Methyl-4-Octanol, The Aggregation Pheromone Of Palmetto Weevil, Rhynchophorus Cruentatus Liebigs Annalen. 1995: 697-698. DOI: 10.1002/Jlac.199519950499 |
0.398 |
|
| 1994 |
Kitahara T, Kinoshita Y, Aono S, Miyake M, Hasegawa T, Watanabe H, Mori K. Synthetic studies on phenazine antibiotics and antheridic acid Pure and Applied Chemistry. 66: 2083-2086. DOI: 10.1351/Pac199466102083 |
0.678 |
|
| 1994 |
Matsuyama K, Mori K. Synthesis of a Stereoisomeric Mixture of 13, 25-, 11, 21- and 11, 23-Dimethylhepta-triacontane, the Contact Sex Pheromone of the Tsetse Fly,Glossina Bioscience, Biotechnology, and Biochemistry. 58: 539-543. DOI: 10.1271/Bbb.58.539 |
0.326 |
|
| 1994 |
Tamura H, Fujita A, Takagi Y, Kitahara T, Mori K. Simple Synthesis of Dehydrololiolide Bioscience, Biotechnology, and Biochemistry. 58: 1902-1903. DOI: 10.1271/Bbb.58.1902 |
0.625 |
|
| 1994 |
Abe T, Mori K. Synthesis of (2S,2’R,3R,4E,8E)-N-2’-Hydroxyoctadecanoyl-1-O-(β-d-glucopyranosyl)-9-methyl-4,8-sphingadienine (Pen III), a Cerebroside Isolated fromPenicillium funiculosumas the Fruiting Inducer againstSchizophyllum commune Bioscience, Biotechnology, and Biochemistry. 58: 1671-1674. DOI: 10.1271/Bbb.58.1671 |
0.338 |
|
| 1994 |
Kiyota H, Mori K. Synthesis of (2S,4R,5S)-2,4,6-Trimethyl-5-heptanolide, a Sex Pheromone Component forMacrocentvus grandii Bioscience, Biotechnology, and Biochemistry. 58: 1120-1122. DOI: 10.1271/Bbb.58.1120 |
0.417 |
|
| 1994 |
Ikemoto T, Kageyama Y, Onuma F, Shibuya Y, Ichimura K, Sakashita K, Mori K. Synthesis and properties of new chiral dopants containing a δ-lactone ring for practical ferroelectric liquid crystal mixtures Liquid Crystals. 17: 729-739. DOI: 10.1080/02678299408037344 |
0.381 |
|
| 1994 |
Watanabe H, Shimizu H, Mori K. Synthesis of Compounds with Juvenile Hormone Activity; XXXI:1Stereocontrolled Synthesis of (+)-Juvabione from a Chiral Sulfoxide Synthesis. 1994: 1249-1254. DOI: 10.1055/S-1994-25674 |
0.665 |
|
| 1994 |
Mori K, Matsushima Y. Synthesis of Mono- and Sesquiterpenoids; XXIII. Synthesis of (E)-endo-Bergamoten-12-oic Acids (α-form, β-form), Moth Oviposition Stimulants Isolated from Wild Tomato Leaves Synthesis. 1994: 417-421. DOI: 10.1055/S-1994-25489 |
0.321 |
|
| 1994 |
Mori K, Amaike M. Pheromone synthesis. Part 166. Synthesis of (2E,5R,6E,8E)-5,7-dimethyldeca-2,6,8-trien-4-one, the major component of the sex pheromone of the Israeli pine bast scale, and its antipode Journal of the Chemical Society-Perkin Transactions 1. 2727-2733. DOI: 10.1039/P19940002727 |
0.359 |
|
| 1994 |
Mori K, Otaka K. Synthesis of sphingofungin D and its stereoisomer at C-14 Tetrahedron Letters. 35: 9207-9210. DOI: 10.1016/0040-4039(94)88467-6 |
0.305 |
|
| 1994 |
Mori K, Murata N. Pheromone Synthesis, CLXVII. Synthesis of All of the Eight Stereoisomers of Methyl 2,6,10-Trimethyltridecanoate, the Male-Produced Pheromone of the Stink Bugs,Euschistus heros andE. obscurus Liebigs Annalen Der Chemie. 1994: 1153-1160. DOI: 10.1002/Jlac.199419941203 |
0.397 |
|
| 1994 |
Mori K, Ogita H. Pheromone Synthesis, CLXIV. Synthesis of (2S, 6Z)-6,8-Nonadien-2-ol, a Pheromone Component of the LeafminerNepticula malella, and Its Antipode Liebigs Annalen Der Chemie. 1994: 1065-1068. DOI: 10.1002/Jlac.199419941104 |
0.48 |
|
| 1994 |
Mori K, Furuuchi T, Kiyota H. Pheromone Synthesis, CLXV. A New Synthesis of (3S,7R,8E,10E)-3,7,9-Trimethyl-8,10-dodecadien-6-one, the Major Component of the Sex Pheromone of the Maritime Pine Scale Liebigs Annalen Der Chemie. 1994: 971-974. DOI: 10.1002/Jlac.199419941003 |
0.405 |
|
| 1994 |
Mori K, Horinaka A, Kido M. Synthetic microbial chemistry. XXVI: Absolute configuration of (+)-xanthocidin as determined by the synthesis of its enantiomers of known stereochemistry European Journal of Organic Chemistry. 1994: 817-825. DOI: 10.1002/Jlac.199419940810 |
0.458 |
|
| 1994 |
Mori K, Argade NP. Pheromone Synthesis, CLXIII. Synthesis of (9Z,25S,26R,43Z)-25,26-Epoxy-9,43-henpentacontadiene and Its Antipode, Components of the Nymph Recognition Pheromone Produced by Nymphs of the CockroachNauphoeta cinerea Liebigs Annalen Der Chemie. 1994: 695-700. DOI: 10.1002/Jlac.199419940711 |
0.629 |
|
| 1994 |
Mori K, Murata N. Pheromone Synthesis, CLXII. Synthesis of Methyl 2,6,10-Trimethyltridecanoate, the Male-Produced Pheromone of the Stink Bugs,Euschistus heros andE. obscurus, as a Stereoisomeric Mixture Liebigs Annalen Der Chemie. 1994: 637-639. DOI: 10.1002/Jlac.199419940617 |
0.374 |
|
| 1994 |
Mori K, Qian Z. Pheromone synthesis. CLX: A new synthesis of the oviposition-deterring pheromone of the European cherry fruit fly Rhagoletis cerasi L. European Journal of Organic Chemistry. 1994: 291-295. DOI: 10.1002/Jlac.199419940311 |
0.39 |
|
| 1994 |
Mori K, Uenishi K. Synthesis of sphingosine relatives, XIV. A new synthesis of symbioramide, a Ca++-ATPase activator fromSymbiodinium sp. Liebigs Annalen Der Chemie. 1994: 41-48. DOI: 10.1002/Jlac.199419940109 |
0.46 |
|
| 1994 |
Mori K, Qian Z. Synthesis of (3R,25R)-3,25-dihydroxyhexacosyl α-D-glucopyranoside, the heterocyst glycolipid of the marine cyanobacteriumNodularia harveyana Liebigs Annalen Der Chemie. 1994: 35-39. DOI: 10.1002/Jlac.199419940108 |
0.36 |
|
| 1993 |
Abo M, Mori K. Synthesis of (R)-Callosobruchusic Acid from Methyl (R)-3-Carboxybutanoate. Bioscience, Biotechnology, and Biochemistry. 57: 265-267. PMID 27314780 DOI: 10.1271/Bbb.57.265 |
0.366 |
|
| 1993 |
Kitahara T, Furusho Y, Mori K. Synthesis of (+)-Turmeronol A, an Inhibitor of Soybean Lipoxygenase, and (+)-ar-Turmerone. Bioscience, Biotechnology, and Biochemistry. 57: 1137-40. PMID 27280998 DOI: 10.1271/Bbb.57.1137 |
0.669 |
|
| 1993 |
Szöcs G, Tóth M, Francke W, Schmidt F, Philipp P, König WA, Mori K, Hansson BS, Löfstedt C. Species discrimination in five species of winter-flying geometrids (Lepidoptera) based on chirality of semiochemicals and flight season. Journal of Chemical Ecology. 19: 2721-35. PMID 24248723 DOI: 10.1007/Bf00980703 |
0.305 |
|
| 1993 |
Kasai T, Watanabe H, Mori K. Synthesis of the enantiomers of lasiol, an acyclic monoterpene alcohol in the mandibular gland secretion of the male ants, Lasius meridionalis. Bioorganic & Medicinal Chemistry. 1: 67-70. PMID 8081839 DOI: 10.1016/S0968-0896(00)82104-5 |
0.62 |
|
| 1993 |
Pinyarat W, Mori K. Synthesis of 2,4-Dimethyl-5-hexanolide, 2,4-Dimethyl-5-heptanolide and 2,4-Dimethyl-5-octanolide, the Lactones Identified in Volatiles from the Heads of the Male Black Garden Ant,Lasius niger Bioscience, Biotechnology, and Biochemistry. 57: 419-421. DOI: 10.1271/Bbb.57.419 |
0.424 |
|
| 1993 |
Takeuchi Y, Mori K. Synthesis of (S,E)-1-Methyl-9-dodecenyl Acetate, the Sex Pheromone of the Hessian Fly,Mayetiola destructor Bioscience, Biotechnology, and Biochemistry. 57: 1967-1968. DOI: 10.1271/Bbb.57.1967 |
0.388 |
|
| 1993 |
Kitahara T, Suzuki N, Koseki K, Mori K. Synthesis of (–)-Allosamizoline, the Pseudoaminosugar Moiety of Allosamidin, a Chitinase Inhibitor Bioscience, Biotechnology, and Biochemistry. 57: 1906-1909. DOI: 10.1271/Bbb.57.1906 |
0.659 |
|
| 1993 |
Brevet J, Mori K. Synthesis of Both the Enantiomers of (6Z,9Z)-cis-3,4-Epoxy-6,9-heptadecadiene, the Pheromone Component of Various Geometrid Moths Bioscience, Biotechnology, and Biochemistry. 57: 1553-1556. DOI: 10.1271/Bbb.57.1553 |
0.402 |
|
| 1993 |
Sakashita K, Ikemoto T, Nakaoka Y, Terada F, Sako Y, Kageyama Y, Mori K. 2-Hydroxy-5,5-dialkyl-δ-valerolactone derivatives as chiral dopants for practical ferroelectric liquid crystals Liquid Crystals. 13: 71-81. DOI: 10.1080/02678299308029054 |
0.338 |
|
| 1993 |
Mori K, Matsushima Y. Synthesis of mono- and sesquiterpenoids. XXII: Synthesis of (+)-pinthunamide, a sesquiterpene metabolite of a fungus, Ampulliferina sp. Synthesis. 1993: 406-410. DOI: 10.1055/S-1993-25873 |
0.438 |
|
| 1993 |
Mori K, Takikawa H, Kido M. Triterpenoid total synthesis. Part 3. Synthesis of meso- and (±)-limatulone, defensive metabolites of the limpet Collisella limatula Journal of the Chemical Society-Perkin Transactions 1. 169-179. DOI: 10.1039/P19930000169 |
0.339 |
|
| 1993 |
Mori K, Amaike M. Synthesis of (S-α-damascone Tetrahedron. 49: 1871-1878. DOI: 10.1016/S0040-4020(01)80543-3 |
0.359 |
|
| 1993 |
Mori K, Harashima S. Pheromone Synthesis, CXLIX. Synthesis of (2E,4E,6R,10S)-4,6,10-Trimethyl-2,4-dodecadien-7-one – the Major Component of the Sex Pheromone of the Maritime Pine Scale (Matsucoccus feytaudi) – and its Three Stereoisomers Liebigs Annalen Der Chemie. 1993: 391-401. DOI: 10.1002/Jlac.199319930165 |
0.422 |
|
| 1993 |
Mori K, Amaike M, Watanabe H. Pheromone Synthesis, CLVIII. New Synthesis and Revision of the Absolute Configuration of the Hemiacetal Pheromone of the Spined Citrus BugBiprorulus bibax Liebigs Annalen Der Chemie. 1993: 1287-1294. DOI: 10.1002/Jlac.1993199301210 |
0.687 |
|
| 1993 |
Mori K, Kiyota H, Malosse C, Rochat D. Pheromone Synthesis, CLVII. Synthesis of the Enantiomers ofsyn-4-Methyl-5-nonanol to Determine the Absolute Configuration of the Naturally Occurring (4S,5S) Isomer Isolated as the Male-produced Pheromone Compound ofRhynchophorus vulneratus andMetamasius hemipterus Liebigs Annalen Der Chemie. 1993: 1201-1204. DOI: 10.1002/Jlac.1993199301194 |
0.469 |
|
| 1993 |
Mori K, Aki S. Diterpenoid Total Synthesis, XXX. Synthesis of the Racemic Form of Tripterifordin, a Novel Anti-HIV Diterpene Lactone fromTripterygium wilfordii Liebigs Annalen Der Chemie. 1993: 97-98. DOI: 10.1002/Jlac.199319930116 |
0.32 |
|
| 1993 |
Mori K, Harashima S. Pheromone synthesis, CLV. Synthesis of (2E,4E,6R,10R)-4,6,10,12-Tetramethyl-2,4-tridecadien-7-one (matsuone) – the Primary Component of the Sex Pheromone of ThreeMatsucoccus Pine Bast Scales – and its Antipode Liebigs Annalen Der Chemie. 1993: 993-1001. DOI: 10.1002/Jlac.1993199301158 |
0.406 |
|
| 1993 |
Mori K, Takayama S, Yoshimura S. Preparative Bioorganic Chemistry, XVII. – Reduction of a Prochiral Diketone, 9-Methyl-trans-decalin-1,8-dione, with Baker's Yeast Liebigs Annalen Der Chemie. 1993: 91-95. DOI: 10.1002/Jlac.199319930115 |
0.399 |
|
| 1993 |
Mori K, Aki S, Kido M. Pheromone synthesis, CXLVII. – Synthesis of (1R,3S,6R,9S,10S)-9,10-Epoxytetrahydroedulan, the Main Component of the Hairpencil Secretion of Male Danaid ButterflyEuploea klugii Liebigs Annalen Der Chemie. 1993: 83-90. DOI: 10.1002/Jlac.199319930114 |
0.421 |
|
| 1993 |
Mori K, Kiyota H, Rochat D. Pheromone Synthesis, CLIV. Synthesis of the Stereoisomers of 3-Methyl-4-octanol to Determine the Absolute Configuration of the Naturally Occurring (3S,4S)-Isomer Isolated as the Male-produced Aggregation Pheromone of the African Palm Weevil,Rhynchophorus phoenicis Liebigs Annalen Der Chemie. 1993: 865-870. DOI: 10.1002/Jlac.1993199301137 |
0.452 |
|
| 1993 |
Mori K, Khlebnikov V. Carotenoids and Degraded Carotenoids, VIII – Synthesis of (+)-Dihydroactinidiolide, (+)- and (−)-Actinidiolide, (+)- and (−)-Loliolide as well as (+)- and (−)-Epiloliolide Liebigs Annalen Der Chemie. 1993: 77-82. DOI: 10.1002/Jlac.199319930113 |
0.399 |
|
| 1993 |
Mori K, Tomioka H, Fukuyo E, Yanagi K. Synthetic Microbial Chemistry, XXV. Synthesis of the Enantiomers of Differolide [4-(2′,5′-Dihydro-2′-oxo-3′-furanyl)-3a,4,5,6-tetrahydro-1(3H)-isobenzofuranone], a Microbial Bioregulator for the Formation of Aerial Mycelium and Spores ofStreptomyces glaucescens Liebigs Annalen Der Chemie. 1993: 671-681. DOI: 10.1002/Jlac.1993199301109 |
0.392 |
|
| 1992 |
Hasegawa T, Kamada A, Mori K. Synthesis of the Enantiomers of 7-Methyl-1, 6-dioxaspiro[4.5]decane, Pheromone of the Common Wasp and the Pine Beetle Bioscience, Biotechnology, and Biochemistry. 56: 838-839. PMID 27286226 DOI: 10.1271/Bbb.56.838 |
0.408 |
|
| 1992 |
Tomioka H, Mori K. Simple Synthesis of a Diastereomeric Mixture of 2-(3',4'-Epoxy-4'-methylcyclohexyl)-6-methyl-2,5-heptadiene, the Pheromone of the Green Stink Bug. Bioscience, Biotechnology, and Biochemistry. 56: 1001. PMID 27280842 DOI: 10.1271/Bbb.56.1001 |
0.403 |
|
| 1992 |
Mori K, Aki S, Kozak J, Norin T, Spielbüchler P, Pedersen JB, Krogsgaard-Larsen P. Synthesis of Mono- and Sesqui-terpenoids. XXI. Synthesis and Absolute Configuration of (E)-3-Formyl-(2,6,6-trimethyl-2-cyclohexenyl)-3-pentenal, a Sesquiterpenoid from a Marine Alga, Caulerpa ashmeadii. Acta Chemica Scandinavica. 46: 625-629. DOI: 10.3891/Acta.Chem.Scand.46-0625 |
0.434 |
|
| 1992 |
Matsuda H, Mori K. Synthesis of Several Analogs of Esterified Cerebroside Isolated from Human and Pig Epidermis Bioscience, Biotechnology, and Biochemistry. 56: 2076-2078. DOI: 10.1271/Bbb.56.2076 |
0.315 |
|
| 1992 |
Pinyarat W, Mori K. Synthesis of the Enantiomers of 2-Dodecanol, a Component of the Hind Leg Tibial Gland Secretion of Worker Ants ofCrematogaster auberti Bioscience, Biotechnology, and Biochemistry. 56: 1673-1673. DOI: 10.1271/Bbb.56.1673 |
0.356 |
|
| 1992 |
Nagano E, Mori K. Synthesis of (+)-Juvabione, a Compound with Juvenile Hormone Activity Bioscience, Biotechnology, and Biochemistry. 56: 1589-1591. DOI: 10.1271/Bbb.56.1589 |
0.353 |
|
| 1992 |
Mori K, Takikawa H, Kido M, Albizati KF, Faulkner DJ. Synthesis of (±)- andMeso-Limatulone, Defensive Triterpene Metabolites of the LimpetCollisella Limatula Natural Product Letters. 1: 59-64. DOI: 10.1080/10575639208048887 |
0.331 |
|
| 1992 |
Brevet J, Mori K. Pheromone synthesis. CXXXIX: Enzymatic preparation of (2S,3R)-4-acetoxy-2,3-epoxybutan-1-ol and its conversion to the epoxy pheromones of the GYpsy moth and the Ruby tiger moth Synthesis. 1992: 1007-1012. DOI: 10.1055/S-1992-26290 |
0.398 |
|
| 1992 |
Shimazaki K, Mori M, Okada K, Chuman T, Kuwahara S, Kitahara T, Mori K, Gotō H, Ōsawa E, Sakakibara K, Hirota M. Combined molecular mechanics (MM2) and molecular orbital (AM1) study of periplanone-b and analogues. Evaluation of biological activity from electronic properties and geometries Journal of the Chemical Society-Perkin Transactions 1. 1167-1173. DOI: 10.1039/P29930001167 |
0.601 |
|
| 1992 |
Mori K, Koga Y. Synthesis and absolute configuration of (−)-stypoldione Bioorganic & Medicinal Chemistry Letters. 2: 391-394. DOI: 10.1016/S0960-894X(00)80153-5 |
0.386 |
|
| 1992 |
Koda Y, Kikuta Y, Kitahara T, Nishi T, Mori K. Comparisons of various biological activities of stereoisomers of methyl jasmonate Phytochemistry. 31: 1111-1114. DOI: 10.1016/0031-9422(92)80243-8 |
0.64 |
|
| 1992 |
Mori K, Fukamatsu K. Pheromone Synthesis, CXXXVII. A New Synthesis of (+)-Grandisol Liebigs Annalen Der Chemie. 1992: 489-493. DOI: 10.1002/Jlac.199219920187 |
0.474 |
|
| 1992 |
Mori K, Qian Z, Watanabe S. Preparative Bioorganic Chemistry, XVI. Synthesis of 3,4′-Dihydroxypropiophenone 3-ß-D-Glucopyranoside, a Constituent ofBetula platyphylla var.japonica, by Enzymatic Transglucosylation Liebigs Annalen Der Chemie. 1992: 485-487. DOI: 10.1002/Jlac.199219920186 |
0.352 |
|
| 1992 |
Mori K, Matsuda H. Synthesis of sphingosine relatives. XII: Synthesis and absolute configuration of the two epimeric aliphatic amino alcohols [(5E, 7E)-2-amino-5,7-tetradecadien-3-ols] isolated from a sponge, Xestospongia sp. European Journal of Organic Chemistry. 1992: 131-137. DOI: 10.1002/Jlac.199219920125 |
0.391 |
|
| 1992 |
Mori K, Ishigami K. Pheromone Synthesis, CXLV. Synthesis of the Enantiomers of Rhynchophorol [(E)-6-Methyl-2-hepten-4-ol], the Male-Produced Aggregation Pheromone of the American Palm Weevil,Rhynchophorus palmarum Liebigs Annalen Der Chemie. 1992: 1195-1198. DOI: 10.1002/Jlac.1992199201196 |
0.436 |
|
| 1992 |
Mori K, Fukamatsu K. Pheromone Synthesis, CXLIV. A Synthesis of (1R,5S)-(+)-Frontalin from (S)-(—)-2-Hydroxyparaconic Acid Liebigs Annalen Der Chemie. 1992: 1191-1193. DOI: 10.1002/Jlac.1992199201195 |
0.424 |
|
| 1992 |
Mori K, Amaike M, Oliver JE. Pheromone Synthesis, CXLIII. Synthesis and Absolute Configuration of the Hemiacetal Pheromone of the Spined Citrus Bug Biprorulus bibax Liebigs Annalen Der Chemie. 1992: 1185-1190. DOI: 10.1002/Jlac.1992199201194 |
0.444 |
|
| 1992 |
Mori K, Itou M. Pheromone Synthesis, CXXXV. Synthesis of (4R,5R,6S,7E,9E)-4,6,8-Trimethyl-7,9-undecadien-5-ol and Its Antipode, the Female Specific Compound of the Woodroach Cryptocercus punctulatus European Journal of Organic Chemistry. 1992: 87-93. DOI: 10.1002/Jlac.199219920118 |
0.397 |
|
| 1992 |
Mori K, Wu J. Pheromone Synthesis, CXXXIV. Synthesis of the Four Possible Stereoisomers of 13,17-Dimethylnonatriacontane, a Kairomone for the Wasp Trichogramma nubilale European Journal of Organic Chemistry. 1992: 83-85. DOI: 10.1002/Jlac.199219920117 |
0.49 |
|
| 1992 |
Mori K, Tomioka H. Pheromone Synthesis, CXL. Synthesis of Four Macrolide Pheromones to Define the Scope and Limitation of Enzymatic Macrolactonization Liebigs Annalen Der Chemie. 1992: 1011-1017. DOI: 10.1002/Jlac.1992199201167 |
0.42 |
|
| 1992 |
Mori K, Kiyota H. Pheromone Synthesis, CXLII. A New Synthesis of (3S,4R)-8-Nonene-3,4-diol, the Key Intermediate for the Synthesis of (+)-endo-Brevicomin European Journal of Organic Chemistry. 1992: 989-992. DOI: 10.1002/Jlac.1992199201163 |
0.5 |
|
| 1991 |
WU J, MORI K. Synthesis of the Enantiomers of 2,6-Dimethyl-6-hepten-1-ol, a Mandibular Gland Secretion of the Male Ant Lasius niger. Agricultural and Biological Chemistry. 55: 2667-2668. DOI: 10.1271/Bbb1961.55.2667 |
0.395 |
|
| 1991 |
KITAHARA T, WARITA Y, ABE M, SEYA M, TAKAGI Y, MORI K. Stereoselective synthesis of methyl epijasmonate. Agricultural and Biological Chemistry. 55: 1013-1017. DOI: 10.1271/Bbb1961.55.1013 |
0.691 |
|
| 1991 |
Mori K, Brevet J. Pheromone Synthesis; CXXXIII.1 Synthesis of Both the Enantiomers of (3Z,9Z)-cis-6,7-Epoxy-3,9-nonadecadiene, a Pheromone Component of Erannis defoliaria Synthesis. 1991: 1125-1129. DOI: 10.1055/S-1991-28403 |
0.383 |
|
| 1991 |
Mori K, Ishikura M, Seu Y. Preparative Bioorganic Chemistry; XIV.1Preparation of (2S,3S)-1-Phenylthio-2,3-pentanediol and (2S,3S)-1-Phenylsulfonyl-2,3-pentanediol by Yeast Reduction of the Corresponding Diketones, and Conversion of the Former to (+)-endo-Brevicomin Synthesis. 1991: 487-490. DOI: 10.1055/S-1991-26502 |
0.364 |
|
| 1991 |
Watanabe H, Mori K. Triterpenoid total synthesis. Part 2. Synthesis of glycinoeclepin A, a potent hatching stimulus for the soybean cyst nematode Journal of the Chemical Society-Perkin Transactions 1. 2919-2934. DOI: 10.1039/P19910002919 |
0.415 |
|
| 1991 |
Schwab E, Bernreuther A, Puapoomchareon P, Mori K, Schreier P. Stereoselective formation of metabolites from 2-methyl-2-hepten-6-one by Botrytis cinerea Tetrahedron: Asymmetry. 2: 471-479. DOI: 10.1016/S0957-4166(00)82172-2 |
0.384 |
|
| 1991 |
Mori K, Harashima S. Assignment of (6R*,10R*)-relative stereochemistry to the major component of the sex pheromone of the maritime pine scale, matsucoccus feytaudi Tetrahedron Letters. 32: 5995-5998. DOI: 10.1016/S0040-4039(00)79447-0 |
0.374 |
|
| 1991 |
Kitahara T, Kiyota H, Kurata H, Mori K. Synthesis of oxygenated eremophilanes, gigantenone, phomenone and phaseolinone, phytotoxins from pathogenic fungi Tetrahedron. 47: 1649-1654. DOI: 10.1016/S0040-4020(01)96908-X |
0.632 |
|
| 1991 |
Kitahara T, Nishi T, Mori K. Synthesis of both the enantiomers of methyl epijasmonate Tetrahedron. 47: 6999-7006. DOI: 10.1016/S0040-4020(01)96154-X |
0.678 |
|
| 1991 |
Mori K, Takikawa H. A new synthesis of the enantiomers of ipsdienol, the pheromone of the IPS bark beetles Tetrahedron. 47: 2163-2168. DOI: 10.1016/S0040-4020(01)96127-7 |
0.416 |
|
| 1991 |
Mori K, Matsuda H. Synthesis of sphingosine relatives, X. Synthesis of (2S,3R4E)-1-O-(β-D-glucopyranosyl)-N-[30′-(linoleoyloxy)triacontanoyl]-4-icosasphingenine, a new esterified cerebroside isolated from human and pig epidermis Liebigs Annalen Der Chemie. 1991: 529-535. DOI: 10.1002/Jlac.199119910197 |
0.337 |
|
| 1991 |
Mori K, Takikawa H. Pheromone synthesis, CXXX. Synthesis of (4S,8S)- and (4S,8R)-4,8-dimethyldecanal, the stereoisomers of the aggregation pheromone of Tribolium castaneum European Journal of Organic Chemistry. 1991: 497-500. DOI: 10.1002/Jlac.199119910189 |
0.391 |
|
| 1991 |
Mori K, Wu J. Pheromone synthesis, CXXIX. Synthesis of the (5S,9S)-isomers of 5,9-Dimethylheptadecane and 5,9-dimethyloctadecane, the major and the minor components of the sex pheromone ofLeucoptera malifoliella costa Liebigs Annalen Der Chemie. 1991: 439-443. DOI: 10.1002/Jlac.199119910180 |
0.417 |
|
| 1991 |
Mori K, Nagano E. Pheromone synthesis, CXXVII. A new synthesis of the enantiomers of grandisol and lineatin European Journal of Organic Chemistry. 1991: 341-344. DOI: 10.1002/Jlac.199119910159 |
0.384 |
|
| 1991 |
Mori K, Harada H, Zagatti P, Cork A, Hall DR. Pheromone synthesis, CXXVI. Synthesis and biological activity of four stereoisomers of 6,10,14‐trimethyl‐2‐pentadecanol, the female‐produced sex pheromone of rice moth (Corcyra cephalonica) European Journal of Organic Chemistry. 1991: 259-267. DOI: 10.1002/Jlac.199119910144 |
0.354 |
|
| 1991 |
Mori K, Nishio H. Synthesis of sphingosine relatives, IX. Synthesis of (2S,3R,4E)-1-O-(β-D-glucopyranosyl)-N- [24-(linoleoyloxy)tetracosanoyl]-4-sphingenine. The structure proposed for the esterified cerebroside in the epidermis of guinea pigs European Journal of Organic Chemistry. 1991: 253-257. DOI: 10.1002/Jlac.199119910143 |
0.36 |
|
| 1991 |
Mori K, Wu J. Pheromone synthesis, CXXV. Synthesis of the four possible stereoisomers of 3,7-dimethylnonadecane, the female sex pheromone of Agromyza frontella Rondani European Journal of Organic Chemistry. 1991: 213-217. DOI: 10.1002/Jlac.199119910138 |
0.47 |
|
| 1991 |
Mori K, Kinsho T. Synthesis of Sphingosine Relatives, XI. Synthesis of wheat grain cerebroside with fruiting‐inducing effect on Schizophyllum commune European Journal of Organic Chemistry. 1991: 1309-1315. DOI: 10.1002/Jlac.1991199101225 |
0.376 |
|
| 1991 |
Mori K, Takahashi Y. Synthetic microbial chemistry, XXIV. Synthesis of antibiotic 1233A, an inhibitor of cholesterol biosynthesis European Journal of Organic Chemistry. 1991: 1057-1065. DOI: 10.1002/Jlac.1991199101183 |
0.326 |
|
| 1991 |
Mori K, Puapoomchareon P. Preparative bioorganic chemistry, XV. Preparation of optically pure 2,4,4-trimethyl-2-cyclohexen-1-ol, a new and versatile chiral building block in terpene synthesis Liebigs Annalen Der Chemie. 1991: 1053-1056. DOI: 10.1002/Jlac.1991199101182 |
0.434 |
|
| 1991 |
Mori K, Wu J. Pheromone synthesis, CXXXI. Synthesis of the four stereoisomers of 6,10,13‐trimethyl‐1‐tetradecanol, the aggregation pheromone of predatory stink bug, Stiretrus anchorago European Journal of Organic Chemistry. 1991: 783-788. DOI: 10.1002/Jlac.1991199101134 |
0.399 |
|
| 1991 |
Mori K, Kamada A, Kido M. Synthesis of the three stereoisomers of auxin-glutaric acid to confirm the non-existence of Kögl's auxin-a and -b Liebigs Annalen Der Chemie. 1991: 775-781. DOI: 10.1002/Jlac.1991199101133 |
0.366 |
|
| 1991 |
Mori K, Koga Y. Diterpenoid total synthesis, XXIX. Synthesis of (±)‐14‐deoxystypoldione, an analogue of the marine natural product stypoldione European Journal of Organic Chemistry. 1991: 769-774. DOI: 10.1002/Jlac.1991199101132 |
0.378 |
|
| 1991 |
Mori K, Fujiwhara M. Synthesis of (4S, 10R, 11S)-4-Methyl Juvenile Hormone I by Using Chiral Building Blocks of Biochemical Origin Israel Journal of Chemistry. 31: 223-227. DOI: 10.1002/ijch.199100026 |
0.337 |
|
| 1990 |
Tengö J, Ågren L, Baur B, Isaksson R, Liljefors T, Mori K, König W, Francke W. Andrena wilkella male bees discriminate between enantiomers of cephalic secretion components. Journal of Chemical Ecology. 16: 429-441. PMID 24263500 DOI: 10.1007/Bf01021775 |
0.331 |
|
| 1990 |
Schulz S, Francke W, König WA, Schurig V, Mori K, Kittmann R, Schneider D. Male pheromone of swift moth,Hepialus hecta L. (Lepidoptera: Hepialidae). Journal of Chemical Ecology. 16: 3511-21. PMID 24263445 DOI: 10.1007/Bf00982114 |
0.389 |
|
| 1990 |
OKADA K, MORI M, KUWAHARA S, KITAHARA T, MORI K, SHIMAZAKI K, CHUMAN T. Behavioral and electroantennogram responses of male American cockroaches to periplanones and their analogs. Agricultural and Biological Chemistry. 54: 575-576. DOI: 10.1271/Bbb1961.54.575 |
0.553 |
|
| 1990 |
EBATA T, MORI K. Synthesis of 1'-epi-stegobinone. Agricultural and Biological Chemistry. 54: 527-530. DOI: 10.1271/Bbb1961.54.527 |
0.422 |
|
| 1990 |
Mori M, Okada K, Shimazaki K, Chuman T, Kuwahara S, Kitahara T, Mori K. X-Ray crystallographic and NOE studies on the conformation of periplanones and their analogues Journal of the Chemical Society-Perkin Transactions 1. 1769-1777. DOI: 10.1039/P19900001769 |
0.579 |
|
| 1990 |
Kitahara T, Miyake M, Kido M, Mori K. A chiral building block with bicyclo[2.2.2]octanone skeleton by the reduction with Baker's yeast. Tetrahedron: Asymmetry. 1: 775-782. DOI: 10.1016/S0957-4166(00)80443-7 |
0.647 |
|
| 1990 |
Mori K, Igarashi Y. Synthesis of (+-)-pa 22-vii, the racemate of the rearrangement product of persoons's periplanone-A Tetrahedron. 46: 5101-5112. DOI: 10.1016/S0040-4020(01)87817-0 |
0.377 |
|
| 1990 |
Uno T, Watanabe H, Mori K. Synthesis of (+)-cassiol, a potent antiulcerogenic compound Tetrahedron. 46: 5563-5566. DOI: 10.1016/S0040-4020(01)87754-1 |
0.642 |
|
| 1990 |
Mori K, Uno T, Kido M. Determination of the absolute configuration of bifurcarenone by the synthesis of its (1'R,2'R)-isomer Tetrahedron. 46: 4193-4204. DOI: 10.1016/S0040-4020(01)86756-9 |
0.394 |
|
| 1990 |
Mori K, Takikawa H. A new synthesis of the four stereoisomers of 3,11-dimethyl-2-nonacosanone, the female-produced sex pheromone of the german cockroach Tetrahedron. 46: 4473-4486. DOI: 10.1016/S0040-4020(01)85576-9 |
0.389 |
|
| 1990 |
Kuwahara S, Mori K. Synthesis of both the enantiomers of hauptmann's periplanone-A and clarification of the structure of Persoons's periplanone-A Tetrahedron. 46: 8083-8092. DOI: 10.1016/S0040-4020(01)81465-4 |
0.337 |
|
| 1990 |
Kuwahara S, Mori K. Synthesis of (-)-periplanone-B a sex pheromone component of the American cockroach (periplaneta americana) Tetrahedron. 46: 8075-8082. DOI: 10.1016/S0040-4020(01)81464-2 |
0.414 |
|
| 1990 |
Sakurai K, Kitahara T, Mori K. Stereocontrolled synthesis of (-)-prezizanol,(-)-prezizaene, their epimers and (-)-allokhusiol Tetrahedron. 46: 761-774. DOI: 10.1016/S0040-4020(01)81359-4 |
0.67 |
|
| 1990 |
Sakurai S, Ohtaki T, Mori H, Fujiwhara M, Mori K. Biological activity of enantiomerically pure forms of insect juvenile hormone I and III in Bombyx mori Cellular and Molecular Life Sciences. 46: 220-221. DOI: 10.1007/Bf02027321 |
0.347 |
|
| 1990 |
Mori K, Fujiwhara M. Synthesis of compounds with juvenile hormone activity, XXVIII. Synthesis of (−)-juvenile hormone I, the antipode of the natural compound Liebigs Annalen Der Chemie. 1990: 369-372. DOI: 10.1002/Jlac.199019900170 |
0.401 |
|
| 1990 |
Mori K, Tamura H. Triterpenoid total synthesis, I. Synthesis of ambrein and Ambrox® Liebigs Annalen Der Chemie. 1990: 361-368. DOI: 10.1002/Jlac.199019900169 |
0.327 |
|
| 1990 |
Mori K, Suzuki N. Synthesis of mono- and sesquiterpenoids, XIX. Synthesis of the enantiomers of ancistrofuran, a defensive compound fromAncistrotermes cavithorax Liebigs Annalen Der Chemie. 1990: 287-292. DOI: 10.1002/Jlac.199019900152 |
0.476 |
|
| 1990 |
Mori K, Puapoomchareon P. Pheromone synthesis, CXVIII. Synthesis of the enantiomers of (E)-1-ethyl-5-methyl-4-heptenyl acetate (quadrilure), the aggregation pheromone ofCathartus quadricollis Liebigs Annalen Der Chemie. 1990: 159-162. DOI: 10.1002/Jlac.199019900127 |
0.49 |
|
| 1990 |
Mori K, Watanabe H, Fujiwhara M, Kuwahara S. Pheromone synthesis, CXXII. (E)- and (Z)-tetradecenyl formate, potent sex pheromone mimics against the yellow peach moth Liebigs Annalen Der Chemie. 1990: 1257-1259. DOI: 10.1002/Jlac.1990199001225 |
0.597 |
|
| 1990 |
Mori K, Itou M, Brossut R. Pheromone synthesis, CXXI. Synthesis of (4R*,5R*,6S*,7E,9E)-4,6,8-trimethyl-7,9-undecadien-5-ol and its isomers to determine the relative stereochemistry of the female specific compound of the woodroachCryptocercus punctulatus Liebigs Annalen Der Chemie. 1990: 1249-1255. DOI: 10.1002/Jlac.1990199001224 |
0.399 |
|
| 1990 |
Mori K, Chiba N. Synthetic microbial chemistry, XXIII. Synthesis of optically active virginiae butanolides A, B, C, and D and other autoregulators from streptomycetes European Journal of Organic Chemistry. 1990: 31-37. DOI: 10.1002/Jlac.199019900105 |
0.355 |
|
| 1990 |
MORI K, UNO T, KIDO M. ChemInform Abstract: Diterpenoid Total Synthesis. Part 28. Determination of the Absolute Configuration of Bifurcarenone by the Synthesis of Its (1′R,2′R)-Isomer. Cheminform. 21. DOI: 10.1002/chin.199042297 |
0.351 |
|
| 1990 |
KITAHARA T, TOUHARA K, WATANABE H, MORI K. ChemInform Abstract: Synthesis of Mono- and Sesquiterpenoids. Part 17. Stereocontrolled Synthesis of Both the Enantiomers of Phaseic Acid and Its Methyl Ester, a Pivotal Metabolite of Abscisic Acid. Cheminform. 21. DOI: 10.1002/chin.199010283 |
0.739 |
|
| 1989 |
Mori K, Kuwahara S. A New Stereoselective Synthesis of (—)-Periplanone-B Heterocycles. 28: 167. DOI: 10.3987/Com-88-S74 |
0.358 |
|
| 1989 |
Mori K, Watanabe H. Recent results in the synthesis of semiochemicals: synthesis of glycinoeclepin A Pure and Applied Chemistry. 61: 543-546. DOI: 10.1351/pac198961030543 |
0.634 |
|
| 1989 |
EBATA T, MORI K. Synthesis of both the enantiomers of (Z)-cis-9,10-epoxy-6-heneicosene. Agricultural and Biological Chemistry. 53: 801-804. DOI: 10.1271/Bbb1961.53.801 |
0.358 |
|
| 1989 |
KINSHO T, MORI K. Synthesis of sphingosine relatives. Part VIII. Synthesis of 3-deoxy analogs of sphingolipids. Agricultural and Biological Chemistry. 53: 2785-2790. DOI: 10.1271/Bbb1961.53.2785 |
0.401 |
|
| 1989 |
KIKUCHI H, MORI K. Synthesis of (-)-biopterin using (S)-ethyl lactate as a starting material. Agricultural and Biological Chemistry. 53: 2095-2100. DOI: 10.1271/Bbb1961.53.2095 |
0.386 |
|
| 1989 |
SAKURAI K, KITAHARA T, MORI K. A simple preparation of (-)-khusimone (1) using electrochemical decarboxylative acetylation. Agricultural and Biological Chemistry. 53: 1449-1450. DOI: 10.1271/Bbb1961.53.1449 |
0.597 |
|
| 1989 |
HARADA H, MORI K. Simple synthesis of a mixture of (E)- and (Z)-5-undecenoic acid, sex pheromone of the varied carpet beetle. Agricultural and Biological Chemistry. 53: 1439-1440. DOI: 10.1271/Bbb1961.53.1439 |
0.369 |
|
| 1989 |
Nakauchi J, Sakashita K, Kageyama Y, Hayashi S, Mori K. Novel Ferroelectric Liquid Crystals Derived from Normal Alkyl Esters of (R)-3-Hydroxybutanoic Acid. The Correlation between Molecular Structure and Mesomorphic Properties Bulletin of the Chemical Society of Japan. 62: 1011-1016. DOI: 10.1246/Bcsj.62.1011 |
0.348 |
|
| 1989 |
Mori K, Igarashi Y. Synthetic confirmation of the structure of the rearrangement product of periplanone-A Tetrahedron Letters. 30: 5145-5148. DOI: 10.1016/S0040-4039(01)93470-7 |
0.333 |
|
| 1989 |
Tóth M, Buser HR, Peña A, Arn H, Mori K, Takeuchi T, Nikolaeva LN, Kovalev BG. Identification of (3Z,6Z)-1,3,6–9,10-epoxyheneicosatriene and (3Z,6Z)-1,3,6–9,10-epoxyeicosatriene in the sex pheromone of hyphantria cunea Tetrahedron Letters. 30: 3405-3408. DOI: 10.1016/S0040-4039(00)99256-6 |
0.32 |
|
| 1989 |
Kitahara T, Touhara K, Watanabe H, Mori K. Stereocontrolled synthesis of both the enantiomers of phaseic acid and its methyl ester, a pivotal metabolite of abscisic acid Tetrahedron. 45: 6387-6400. DOI: 10.1016/S0040-4020(01)89516-8 |
0.751 |
|
| 1989 |
Mori K. Synthesis of optically active pheromones Tetrahedron. 45: 3233-3298. DOI: 10.1016/S0040-4020(01)81007-3 |
0.332 |
|
| 1989 |
Mori K, Uno T. Synthesis and structure revision of bifurcarenone, a unique monocyclic diterpene in combination with a hydroquinone C7 unit as an inhibitor of mitotic cell division Tetrahedron. 45: 1945-1958. DOI: 10.1016/S0040-4020(01)80058-2 |
0.322 |
|
| 1989 |
Mori K, Takaishi H. Synthesis of monocerin, an antifungal, insecticidal and phytotoxic heptaketide metabolite of exserohilum monoceras Tetrahedron. 45: 1639-1646. DOI: 10.1016/S0040-4020(01)80027-2 |
0.36 |
|
| 1989 |
Mori K, Itou M. Pheromone Synthesis, CXV Synthesis of (Z)‐2‐Ochtoden‐1‐ol, (E)‐2‐Ochtoden‐1‐al, and (Z)‐2‐Ochtoden‐1‐al, the Pheromone Components of the Boll Weevil (Anthonomus grandis) European Journal of Organic Chemistry. 1989: 969-973. DOI: 10.1002/Jlac.198919890253 |
0.346 |
|
| 1989 |
Mori K, Kikuchi H. Synthesis of (-)-Biopterin Liebigs Annalen Der Chemie. 1989: 963-967. DOI: 10.1002/Jlac.198919890252 |
0.366 |
|
| 1989 |
Mori K, Chiba N. Preparative Bioorganic Chemistry, XI Preparation of the Enantiomers of Paraconic Acid Employing Lipase‐Mediated Asymmetric Hydrolysis of Prochiral Diacetates as the Key Step European Journal of Organic Chemistry. 1989: 957-962. DOI: 10.1002/Jlac.198919890251 |
0.386 |
|
| 1989 |
Mori K, Takaishi H. Synthesis of Mono- and Sesquiterpenoids, XVI Synthesis of (-)-Pereniporins A and B, Sesquiterpene Antibiotics from a Basidiomycete Liebigs Annalen Der Chemie. 1989: 939-943. DOI: 10.1002/Jlac.198919890248 |
0.433 |
|
| 1989 |
Mori K, Takaishi H. Synthesis of Mono- and Sesquiterpenoids, XV Synthesis of (-)-Warburganal, an Insect Antifeedant Liebigs Annalen Der Chemie. 1989: 695-697. DOI: 10.1002/Jlac.198919890216 |
0.475 |
|
| 1989 |
Mori K, Kikuchi H. A New Synthesis of (-)-Biopterin Employing 5-Deoxy-L-ribose as a Key Intermediate Liebigs Annalen Der Chemie. 1989: 1267-1269. DOI: 10.1002/Jlac.1989198902102 |
0.316 |
|
| 1989 |
Mori K, Ishikura M. Pheromone Synthesis, CXVII Synthesis of Sitophilate, the Aggregation Pheromone of Sitophilus granarius L., and Its Antipode European Journal of Organic Chemistry. 1989: 1263-1265. DOI: 10.1002/Jlac.1989198902101 |
0.473 |
|
| 1989 |
Mori K, Puapoomchareon P. Pheromone Synthesis, CXVI Conversion of the Enantiomers of Sulcatol to the Enantiomers ofcis-Pityol, a Volatile Compound from the Elm Bark BeetlePteleobius vittatus Liebigs Annalen Der Chemie. 1989: 1261-1262. DOI: 10.1002/Jlac.1989198902100 |
0.413 |
|
| 1989 |
Mori K, Takeuchi T. Pheromone Synthesis, CXIII. Synthesis of the Enantiomers of (3Z,6Z)‐cis‐9,10‐Epoxy‐1,3,6‐henicosatriene and (3Z,6Z)‐cis‐9,10‐Epoxy‐1,3,6‐icosatriene, the New Pheromone Components of Hyphantria cunea European Journal of Organic Chemistry. 1989: 453-457. DOI: 10.1002/Jlac.198919890180 |
0.454 |
|
| 1989 |
Mori K, Kamada A, Mori H. Synthetic Microbial Chemistry, XXI. Synthesis of Differanisole A, an Inducer of Differentiation Liebigs Annalen Der Chemie. 1989: 303-305. DOI: 10.1002/Jlac.198919890153 |
0.427 |
|
| 1989 |
Mori K, Fujiwhara M. Synthesis of Compounds with Juvenile Hormone Activity, XXVII. Synthesis of Enantiomerically Pure (10R,11S)-(+)-Juvenile Hormone 0 Liebigs Annalen Der Chemie. 1989: 41-44. DOI: 10.1002/Jlac.198919890109 |
0.422 |
|
| 1989 |
Mori K, Kisida H. Syntheses of Pterocarpans, II. Synthesis of Both the Enantiomers of Pisatin Liebigs Annalen Der Chemie. 1989: 35-39. DOI: 10.1002/Jlac.198919890108 |
0.346 |
|
| 1988 |
Asakawa Y, Dawson GW, Griffiths DC, Lallemand JY, Ley SV, Mori K, Mudd A, Pezechk-Leclaire M, Pickett JA, Watanabe H, Woodcock CM, Zhong-Ning Z. Activity of drimane antifeedants and related compounds against aphids, and comparative biological effects and chemical reactivity of (-)- and (+)-polygodial. Journal of Chemical Ecology. 14: 1845-55. PMID 24277098 DOI: 10.1007/Bf01013481 |
0.584 |
|
| 1988 |
KITAHARA T, MORI K. Total syntheses of periplanone-B, major sex excitant and attractant pheromone of American cockroach, Periplaneta americana L. Journal of Synthetic Organic Chemistry, Japan. 46: 108-120. DOI: 10.5059/Yukigoseikyokaishi.46.108 |
0.673 |
|
| 1988 |
Sugai T, Mori K. Preparative Bioorganic Chemistry; 8.1Efficient Enzymatic Preparation of (1R,4S)-(+)-4-Hydroxy-2-cyclopentenyl Acetate Synthesis. 1988: 19-22. DOI: 10.1055/S-1988-27454 |
0.407 |
|
| 1988 |
Mori K, Tsuji M. SYnthesis and absolute configuration of (−)-pentalenolactone E methyl ester Tetrahedron. 44: 2835-2842. DOI: 10.1016/S0040-4020(88)90019-1 |
0.402 |
|
| 1988 |
Mori K, Koseki K. Synthesis of trichostatin a, a potent differentiation inducer of friend leukemic cells, and its antipode Tetrahedron. 44: 6013-6020. DOI: 10.1016/S0040-4020(01)89789-1 |
0.372 |
|
| 1988 |
Kitahara T, Horiguchi A, Mori K. The synthesis of (-)-sirenin. sperm attractant of the water mold Tetrahedron. 44: 4713-4720. DOI: 10.1016/S0040-4020(01)86174-3 |
0.663 |
|
| 1988 |
Kitahara T, Kurata H, Mori K. Efficient synthesis of the natural enantiomer of sporogen-AO 1 (13-desoxyphomenone) A sporogenic sesquiterpene from aspergillus oryzae Tetrahedron. 44: 4339-4349. DOI: 10.1016/S0040-4020(01)86136-6 |
0.699 |
|
| 1988 |
Mori K, Seu Y. A new synthesis of (-)-α-multistriatin, the pheromone of the smaller european elm bark beetle Tetrahedron. 44: 1035-1038. DOI: 10.1016/S0040-4020(01)85883-X |
0.44 |
|
| 1988 |
Mori K, Fujiwhara M. Synthesis of enantiomerically pure (10,11)-(+)-juvenile hormones I and II Tetrahedron. 44: 343-354. DOI: 10.1016/S0040-4020(01)85826-9 |
0.398 |
|
| 1988 |
Mori K, Takeuchi T. Synthesis of punaglandin 4 by means of enzymatic resolution of the key chlorocyclopentene derivative Tetrahedron. 44: 333-342. DOI: 10.1016/S0040-4020(01)85825-7 |
0.453 |
|
| 1988 |
Mori K, Ogoche JIJ. Pheromone synthesis, CXI. An enzyme-mediated synthesis of both enantiomers of seudenol and 1-methyl-2-cyclohexen-1-ol, the aggregation pheromones ofDendroctonus pseudotsugae Liebigs Annalen Der Chemie. 1988: 903-905. DOI: 10.1002/Jlac.198819880915 |
0.393 |
|
| 1988 |
Mori K, Yoshimura T, Sugai T. Pheromone synthesis, CX. Synthesis of (4S,5R)-5-hydroxy-4-methyl-3-heptanone (Sitophilure), the aggregation pheromone ofSitophilus oryzae andS. zeamais Liebigs Annalen Der Chemie. 1988: 899-902. DOI: 10.1002/Jlac.198819880914 |
0.438 |
|
| 1988 |
Mori K, Takeuchi T. Brassinolide and its analogues, VIII. Synthesis of 25-methyldolichosterone, 25-methyl-2,3-diepidolichosterone, 25-methylcastasterone and 25-methylbrassinolide Liebigs Annalen Der Chemie. 1988: 815-818. DOI: 10.1002/Jlac.198819880819 |
0.366 |
|
| 1988 |
Mori K, Kinsho T. Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated fromTetragonia tetragonoides Liebigs Annalen Der Chemie. 1988: 807-814. DOI: 10.1002/Jlac.198819880818 |
0.403 |
|
| 1988 |
Mori K, Kisida H. Syntheses of pterocarans, I. Synthesis of both the enantiomers of pterocarpin Liebigs Annalen Der Chemie. 1988: 721-723. DOI: 10.1002/Jlac.198819880716 |
0.422 |
|
| 1988 |
Mori K, Igarashi Y. Pheromone synthesis, CIX. Synthesis of the four stereoisomers of 6,12‐dimethyl‐2‐pentadecanone, the sex pheromone of Diabrotica balteata LeConte Liebigs Annalen Der Chemie. 1988: 717-720. DOI: 10.1002/Jlac.198819880715 |
0.403 |
|
| 1988 |
Mori K, Puapoomchareon P. Pheromone synthesis, CVI. Synthesis of all of the four stereoisomers of tetrahydro-2,2,6-trimethyl-2H-pyran-3-ol, a volatile compound from the elm bark beetlePteleobius vittatus Liebigs Annalen Der Chemie. 1988: 175-177. DOI: 10.1002/Jlac.198819880212 |
0.385 |
|
| 1988 |
Mori K, Nakazono Y. Pheromone synthesis, CV. Synthesis of lactone components of the pheromone ofAnastrepha suspensa, suspensolide, and the enantiomers of anastrephin and epianastrephin Liebigs Annalen Der Chemie. 1988: 167-174. DOI: 10.1002/Jlac.198819880211 |
0.375 |
|
| 1988 |
Mori K, Komatsu M. Synthetic microbial chemistry, XVII. Synthesis of the complement inhibitor (−)-K-76 and of related compounds Liebigs Annalen Der Chemie. 1988: 107-119. DOI: 10.1002/Jlac.198819880203 |
0.304 |
|
| 1988 |
Mori K, Tamura H. Synthesis of mono- and sesquiterpenoids, X. Synthesis of sporogen-AO 1 (13-deoxyphomenone), a sporogenic sesquiterpene fromAspergillus oryzae Liebigs Annalen Der Chemie. 1988: 97-105. DOI: 10.1002/Jlac.198819880202 |
0.38 |
|
| 1988 |
Mori K, Igarashi Y. Pheromone synthesis, CIV. Synthesis of the enantiomers of α-Phellandren-8-ol (p-mentha-1,5-dien-8-ol), a monoterpene from bark beetles Liebigs Annalen Der Chemie. 1988: 93-95. DOI: 10.1002/Jlac.198819880116 |
0.43 |
|
| 1988 |
Mori K, Sakai T. Synthetic microbial chemistry, XVI. Synthesis of patulolides A, B, and C, new macrolides isolated fromPenicillium urticae Liebigs Annalen Der Chemie. 1988: 13-17. DOI: 10.1002/Jlac.198819880104 |
0.367 |
|
| 1988 |
KITAHARA T, HORIGUCHI A, MORI K. ChemInform Abstract: Synthetic Microbial Chemistry. Part 19. The Synthesis of (-)-Sirenin, Sperm Attractant of the Water Mold Allomyces macrogynus. Cheminform. 19. DOI: 10.1002/chin.198850305 |
0.591 |
|
| 1988 |
KITAHARA T, KURATA H, MORI K. ChemInform Abstract: Synthetic Microbial Chemistry. Part 18. Efficient Synthesis of the Natural Enantiomer of Sporogen-AO 1 (13-Desoxyphomenone), a Sporogenic Sesquiterpene from Aspergillus oryzae. Cheminform. 19. DOI: 10.1002/chin.198847298 |
0.648 |
|
| 1987 |
Walgenbach CA, Phillips JK, Burkholder WE, King GG, Slessor KN, Mori K. Determination of chirality in 5-hydroxy-4-methyl-3-heptanone, the aggregation pheromone ofSitophilus oryzae (L.) andS. zeamais Motschulsky. Journal of Chemical Ecology. 13: 2159-69. PMID 24301654 DOI: 10.1007/Bf01012564 |
0.371 |
|
| 1987 |
EBATA T, MORI K. Pheromone systhesis. Part 103. Synthesis and absolute configuration of serricorole and serricorone, sex pheromone components of cigarette beetle. Agricultural and Biological Chemistry. 51: 2925-2928. DOI: 10.1271/Bbb1961.51.2925 |
0.422 |
|
| 1987 |
UMEMURA T, MORI K. Synthesis of sphingosine relatives. Part V Synthesis of both 2,3-erythro-and 2,3-threo-isomers of aplidiasphingosine, a marine terpenoid. Agricultural and Biological Chemistry. 51: 217-224. DOI: 10.1271/Bbb1961.51.217 |
0.411 |
|
| 1987 |
UMEMURA T, MORI K. Synthesis of sphingosine relatives. Part VI. Stereocontrolled synthesis of (2R,3R,5R,13S,14R)-(+)-aplisiasphingosine, a marine terpenoid. Agricultural and Biological Chemistry. 51: 1973-1982. DOI: 10.1271/Bbb1961.51.1973 |
0.356 |
|
| 1987 |
ABURATANI M, TAKEUCHI T, MORI K. Synthesis of brassinolide. Part IV. Facile syntheses of brassinosteroids. Brassinolide, castasterone, teasterone and typhasterol. Agricultural and Biological Chemistry. 51: 1909-1913. DOI: 10.1271/Bbb1961.51.1909 |
0.335 |
|
| 1987 |
SENDA S, MORI K. Pheromone synthesis. Part 99. Synthesis of (-)-invictolide, the pheromone component of the red imported fire ant. Agricultural and Biological Chemistry. 51: 1379-1384. DOI: 10.1271/Bbb1961.51.1379 |
0.457 |
|
| 1987 |
KITAHARA T, MIURA K, WARITA Y, TAKAGI Y, MORI K. Synthesis of (.+-.)-methyl epijasmonate and (.+-.)-methyl cucurbate. Agricultural and Biological Chemistry. 51: 1129-1133. DOI: 10.1271/Bbb1961.51.1129 |
0.648 |
|
| 1987 |
Maemoto S, Mori K. Synthesis of (4R,5S,11R)-(−)-Cladospolide A, a Phytotoxic Macrolide fromCladosporium cladosporioides Chemistry Letters. 16: 109-112. DOI: 10.1246/Cl.1987.109 |
0.397 |
|
| 1987 |
Ikunaka M, Mori K. Synthesis of Both Enantiomers of 9-Ethyl-1,7-dioxaspiro[5.5]-undecan-4-one, the Key Intermediate in the Synthesis of Talaromycins A and B Agricultural and Biological Chemistry. 51: 565-571. DOI: 10.1080/00021369.1987.10868025 |
0.423 |
|
| 1987 |
Umemura T, Mori K. Synthesis of Both 2,3-erythro-and 2,3-threo-lsomersof Aplidiasphingosine, a Marine Terpenoid Agricultural and Biological Chemistry. 51: 217-224. DOI: 10.1080/00021369.1987.10867967 |
0.356 |
|
| 1987 |
Aburatani M, Takeuchi T, Mori K. A Simple Synthesis of Steroidal 3α,5-Cyclo-6-ones and their Efficient Transformation to Steroidal 2-En-6-ones Synthesis. 1987: 181-183. DOI: 10.1055/S-1987-27882 |
0.352 |
|
| 1987 |
Mori K, Ikunaka M. Synthesis of (-)-talaromycins a and b Tetrahedron. 43: 45-58. DOI: 10.1016/S0040-4020(01)89929-4 |
0.397 |
|
| 1987 |
Kitahara T, Mori M, Mori K. Total synthesis of (-)-periplanone-B, natural major sex-excitant pheromone of the american cockroach, Tetrahedron. 43: 2689-2699. DOI: 10.1016/S0040-4020(01)86874-5 |
0.666 |
|
| 1987 |
Mori K, Mori H. Synthesis of both the enantiomers of juvenile hormone III Tetrahedron. 43: 4097-4106. DOI: 10.1016/S0040-4020(01)83448-7 |
0.348 |
|
| 1987 |
Mori K, Komatsu N. Synthesis of (+)-baiyunol, the diterpene aglycone of the sweet glycoside baiyunoside Tetrahedron. 43: 3409-3412. DOI: 10.1016/S0040-4020(01)81631-8 |
0.465 |
|
| 1987 |
Mori K, Maemoto S. Synthetic microbial chemistry, XV. Synthesis of (2E,4R,5S,11R)-(−)-Cladospolide A, a Phytotoxic Macrolide fromCladosporium cladosporioides Liebigs Annalen Der Chemie. 1987: 863-869. DOI: 10.1002/Jlac.198719870841 |
0.381 |
|
| 1987 |
Mori K, Kuwahara S. Synthesis of the Methyl Ester of (2R,4R,6R,8R)-2,4,6,8-Tetramethylundecanoic Acid, an Acid Component of the Preen-Gland Wax of the Graylag Goose,Anser anser Liebigs Annalen Der Chemie. 1987: 555-556. DOI: 10.1002/Jlac.198719870377 |
0.376 |
|
| 1987 |
Mori K, Ikunaka M. Optical Rotatory Dispersion of Spiroacetals Liebigs Annalen Der Chemie. 1987: 333-336. DOI: 10.1002/Jlac.198719870330 |
0.348 |
|
| 1987 |
Mori K, Puapoomchareon P. Pheromone Synthesis, XCVIII. Conversion of the Enantiomers of Sulcatol (6-Methyl-5-hepten-2-ol) to the Enantiomers of Pityol [trans-2-(1-Hydroxy-1-methylethyl)-5-methyltetrahydrofuran], a Male-Specific Attractant of the Bark BeetlePityophthorus pityographus Liebigs Annalen Der Chemie. 1987: 271-272. DOI: 10.1002/Jlac.198719870321 |
0.409 |
|
| 1987 |
MORI K, HAZRA BG, PFEIFFER RJ, GUPTA AK, LINDGREN BS. ChemInform Abstract: Pheromone Synthesis. Part 101. Synthesis and Bioactivity of Optically Active Forms of 1-Methyl-2-cyclohexen-1-ol, an Aggregation Pheromone of Dendroctonus pseudotsugae. Cheminform. 18. DOI: 10.1002/chin.198741384 |
0.303 |
|
| 1987 |
MORI K, SEU Y. ChemInform Abstract: Pheromone Synthesis. Part 96. Synthesis of Both the Enantiomers of 7-Ethyl-5-methyl-6,8-dioxabicyclo(3.2.1)oct-3-ene. The Mus musculus (House Mouse) Pheromone. Cheminform. 18. DOI: 10.1002/chin.198714362 |
0.342 |
|
| 1986 |
Mochizuki K, Mori M, Chuman T, Kohno M, Ohnishi A, Watanabe H, Mori K. Reinvestigation of anhydroserricornin, (2S,3S)-2,6-diethyl-3,5-dimethyl-3,4-dihydro-2H-pyran, as a sex pheromone component for male cigarette beetle. Journal of Chemical Ecology. 12: 179-86. PMID 24306407 DOI: 10.1007/BF01045601 |
0.545 |
|
| 1986 |
Mori M, Mochizuki K, Kohno M, Chuman T, Ohnishi A, Watanabe H, Mori K. Inhibitory action of (4S,6S,7R)-isomer to pheromonal activity of serricornin, (4S,6S,7S)-7-Hydroxy-4,6-dimethyl-3-nonanone. Journal of Chemical Ecology. 12: 83-9. PMID 24306398 DOI: 10.1007/BF01045592 |
0.571 |
|
| 1986 |
SATO R, ABE N, SUGIE H, KATO M, MORI K, TAMAKI Y. Biological Activity of the Chiral Sex Pheromone of the Peach Leafminer Moth, Lyonetia clerkella LINNE(Lepidoptera : Lyonetiidae) Applied Entomology and Zoology. 21: 478-480. DOI: 10.1303/Aez.21.478 |
0.309 |
|
| 1986 |
FUNAKI Y, KAWAI G, MORI K. Synthesis of sphingosine relatives. Part IV. Synthesis and biological activity of the isomers and analogs of (4E,8E,2S,3R,2'R)-N-2'-hydroxyhexadecanoyl-9-methyl-4,8-sphingadienine, the ceramide portion of the fruiting-inducing cerebroside in a basidiomycete Schizophyllum commune. Agricultural and Biological Chemistry. 50: 615-623. DOI: 10.1271/Bbb1961.50.615 |
0.434 |
|
| 1986 |
HAYASHI S, MORI K. A new synthesis of hepialone ((R)-2-ethyl-6-methyl-2,3-dihydro-4H-pyran-4-one), the principal component from male sex scales of the ghost moth, Hepialus californicus B. Agricultural and Biological Chemistry. 50: 3209-3210. DOI: 10.1271/Bbb1961.50.3209 |
0.399 |
|
| 1986 |
SUGAI T, TOJO H, MORI K. Diterpenoid total synthesis. Part 25 Synthesis of (4aR, 10aS)-(-)-8-methoxy-1,1,4a-trimethyl-2-oxo-1,2,3,4,4a,9,10,10a-octahydrophenanthrene, an optically active intermediate for the synthesis of diterpenes. Agricultural and Biological Chemistry. 50: 3127-3132. DOI: 10.1271/Bbb1961.50.3127 |
0.302 |
|
| 1986 |
ABURATANI M, TAKEUCHI T, MORI K. Efficient synthesis of (22R,23R,24S)-22,23-isopropylidenedioxy-5.ALPHA.-ergost-2-en-6-one, a key intermediate in the preparation of brassinolide. Agricultural and Biological Chemistry. 50: 3043-3047. DOI: 10.1271/Bbb1961.50.3043 |
0.384 |
|
| 1986 |
FUJIWHARA M, MORI K. Pheromone synthesis. Part 90 Synthesis of both the enantiomers of 3-octanol, the pheromone of various species of ants. Agricultural and Biological Chemistry. 50: 2925-2927. DOI: 10.1271/Bbb1961.50.2925 |
0.396 |
|
| 1986 |
SEU Y, MORI K. Pheromone synthesis. Part 89 A new synthesis of (-)-exo-brevicomin. Agricultural and Biological Chemistry. 50: 2923-2924. DOI: 10.1271/Bbb1961.50.2923 |
0.428 |
|
| 1986 |
KITAHARA T, HAMAGUCHI K, WARITA Y, TAKAGI Y, MORI K. A simple and efficient synthesis of (.+-.)-methyl dihydroepijasmonate. Agricultural and Biological Chemistry. 50: 1867-1872. DOI: 10.1271/Bbb1961.50.1867 |
0.669 |
|
| 1986 |
KISHI T, WADA K, MARUMO S, MORI K. Brassinolide and its analogs. Part VII. Synthesis of brassinolide analogs with a modified ring B and their plant growth-promoting activity. Agricultural and Biological Chemistry. 50: 1821-1830. DOI: 10.1271/Bbb1961.50.1821 |
0.395 |
|
| 1986 |
SAKAI T, MORI K. Pheromone synthesis. Part 82. New synthesis of the macrolide pheromones of the rusty grain beetle, Cryptolestes ferrugineus stephens. Agricultural and Biological Chemistry. 50: 177-183. DOI: 10.1271/Bbb1961.50.177 |
0.336 |
|
| 1986 |
SAKAI T, HAMAMOTO H, MORI K. Pheromone synthesis. Part 85. New synthesis of macrolide pheromones of the flat grain beetle, Cryptolestes pusillus Schoenherr. Agricultural and Biological Chemistry. 50: 1621-1627. DOI: 10.1271/Bbb1961.50.1621 |
0.384 |
|
| 1986 |
Kitahara T, Mori M, Koseki K, Mori K. Total synthesis of (−)-periplanone-B, the sex pheromone of the American cockroach Tetrahedron Letters. 27: 1343-1346. DOI: 10.1016/S0040-4039(00)84254-9 |
0.629 |
|
| 1986 |
Mori K, Kato M. Synthesis and absolute configuration of (+)-hernandulcin, a new sesquiterpene with intensely sweet taste Tetrahedron Letters. 27: 981-982. DOI: 10.1016/S0040-4039(00)84154-4 |
0.459 |
|
| 1986 |
Mori K, Seu Y. Synthesis of both the enantiomers of 7-ethyl-5-methyl-6,8-dioxabicyclo[3.2.1]oct-3-ene, the (house mouse) pheromone Tetrahedron. 42: 5901-5904. DOI: 10.1016/S0040-4020(01)96072-7 |
0.405 |
|
| 1986 |
Mori K, Kato M. Synthesis of (6s,1's)-(+)-hernandulcin, a sweetner, and its stereoisomers Tetrahedron. 42: 5895-5900. DOI: 10.1016/S0040-4020(01)96071-5 |
0.408 |
|
| 1986 |
Mori K, Tamura H. A natural product was shown to be of low optical purity: synthesis of (2S,5R,6E,8E)-2,5-epoxy-6,8-megastigmadiene, its (6Z,8E)-isomer and (2S,6R,7S,8E)-2,7-epoxy-4,8-megastigmadiene. The constituents of osmanthus absolute Tetrahedron. 42: 2643-2646. DOI: 10.1016/S0040-4020(01)90549-6 |
0.354 |
|
| 1986 |
Mori K, Kuwahara S. Stereochemistry of lardolure : The aggregation pheromone of the acarid mite, lardoglyphus konoi Tetrahedron. 42: 5545-5550. DOI: 10.1016/S0040-4020(01)88158-8 |
0.332 |
|
| 1986 |
Mori K, Kuwahara S. Synthesis of both the enantiomers of lardolure, the aggregation pheromone of the acarid mite, Tetrahedron. 42: 5539-5544. DOI: 10.1016/S0040-4020(01)88157-6 |
0.371 |
|
| 1986 |
Mori K, Mori H. Synthesis of both the enantiomers of q-methyl pisiferic acid, a mite growth regulator isolated from endl Tetrahedron. 42: 5531-5538. DOI: 10.1016/S0040-4020(01)88156-4 |
0.359 |
|
| 1986 |
Mori K, Nakazono Y. Synthesis of both the enantiomers invictolide, a pheromone component of the red imported fire ant Tetrahedron. 42: 6459-6464. DOI: 10.1016/S0040-4020(01)88108-4 |
0.361 |
|
| 1986 |
Mori K, Komatsu M, Kido M, Nakagawa K. A simple biogenetic-type synthesis of magnosalicin. A new neolignan with antiallergy activity isolated from Tetrahedron. 42: 523-528. DOI: 10.1016/S0040-4020(01)87450-0 |
0.398 |
|
| 1986 |
Mori K, Tsuji M. A new synthesis of (+)-6a-carbaprostaglandin I2 employing yeast reduction of a β-keto ester derived from -bicyclo[3.3.0] octane-3,7-dione as the key-step Tetrahedron. 42: 435-444. DOI: 10.1016/S0040-4020(01)87443-3 |
0.376 |
|
| 1986 |
Mori K, Watanabe H. Enhancement of optical purity of a product by removing unwanted diastereomers in the course of a chiral synthesis: new synthesis of the stereoisomers of 2,8-dimethyl-1,7-dioxaspiro[5.5]undecane, the pheromone of Tetrahedron. 42: 295-304. DOI: 10.1016/S0040-4020(01)87431-7 |
0.645 |
|
| 1986 |
Mori K, Mori H, Yanai M. Synthesis of (2S,4aS,8aR)-(-)-1,1,4a-trimethyl-2-decalol, an inhibitor of steroid biosynthesis Tetrahedron. 42: 291-294. DOI: 10.1016/S0040-4020(01)87430-5 |
0.303 |
|
| 1986 |
Mori K, Nakazono Y. Synthesis of both the enantiomers of dihydroactinidiolide. a pheromone component of the red imported fire ant Tetrahedron. 42: 283-290. DOI: 10.1016/S0040-4020(01)87429-9 |
0.359 |
|
| 1986 |
Mori K, Watanabe H. Synthesis of both the enantiomers of polygodial, an insect antifeedant sesouiterpene Tetrahedron. 42: 273-281. DOI: 10.1016/S0040-4020(01)87428-7 |
0.653 |
|
| 1986 |
Mori K, Ebata T. Syntheses of optically active pheromones with an epoxy ring, (+)-disparlure and both the enantiomers of (3z,6z)--9,10-epoxy-3,6-heneicosadiene Tetrahedron. 42: 3471-3478. DOI: 10.1016/S0040-4020(01)87314-2 |
0.401 |
|
| 1986 |
Mori K, Ebata T. Synthesis of all of the four possible stereoisomers of 5-hydroxy-4-methyl-3-heptanone (sitophilure), the aggregation pheromone of the rice weevil and the maize weevil Tetrahedron. 42: 4421-4426. DOI: 10.1016/S0040-4020(01)87281-1 |
0.406 |
|
| 1986 |
Mori K, Ebata T. Synthesis of (2,3,1')-stegobinone, the pheromone of the drugstore beetle, with stereocontrol at C-2 and C-1' Tetrahedron. 42: 4413-4420. DOI: 10.1016/S0040-4020(01)87280-X |
0.416 |
|
| 1986 |
Mori K, Kisida H. Synthesis of both the enantiomers of the heterocyclic pheromones isolated from the male swift moth l Tetrahedron. 42: 5281-5290. DOI: 10.1016/S0040-4020(01)82077-9 |
0.379 |
|
| 1986 |
Mori K, Ebata T. Synthesis of (2,3,1',2')-stegobiol, a new component of the drugstore beetle pheromone Tetrahedron. 42: 4685-4689. DOI: 10.1016/S0040-4020(01)82049-4 |
0.414 |
|
| 1986 |
Mori K, Seu Y. Pheromone Synthesis, LXXXI1) New Synthesis of the Enantiomers of exo-Brevicomin, the Pheromone of Dendroctonus brevicomis Le Conte Liebigs Annalen Der Chemie. 1986: 205-209. DOI: 10.1002/Jlac.198619860118 |
0.426 |
|
| 1986 |
MORI K, KOMATSU M, KIDO M, NAKAGAWA K. ChemInform Abstract: Synthesis of Lignans. Part 2. A Simple Biogenetic-Type Synthesis of Magnosalicin, a New Neolignan with Antiallergy Activity Isolated from Magnolia salicifolia. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198621310 |
0.401 |
|
| 1986 |
Mori K, Seu Y-. Pheromone Synthesis-. Part 81. New Synthesis of the Enantiomers of exo-Brevicomin, the Pheromone of Dendroctonus brevicomis Le Conte. Cheminform. 17. DOI: 10.1002/Chin.198616368 |
0.433 |
|
| 1986 |
KITAHARA T, KURATA H, MATSUOKA T, MORI K. ChemInform Abstract: Synthetic Microbial Chemistry. Part 12. Synthesis of Both the Enantiomers of Sclerosporin and Sclerosporal, Sporogenic Substance of Sclerotinia fructicola. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198613340 |
0.651 |
|
| 1986 |
Mori K, Soga H, Ikunaka M. Pheromone Syntheses. Part 78. Synthesis of the Four Thermodynamically Stable Stereoisomers of 2,7-Dimethyl-1,6-dioxaspiro[4.6]undecane, a Component of the Volatile Secretion from the Mandibular Glands of Andrena haemorrhoa F. Cheminform. 17. DOI: 10.1002/Chin.198608323 |
0.337 |
|
| 1985 |
YABUTA G, ICHIKAWA Y, KITAHARA T, MORI K. Syntheses of the proposed structures of sclerosporene with a guaiane skeleton in optically active form. Agricultural and Biological Chemistry. 49: 495-499. DOI: 10.1271/Bbb1961.49.495 |
0.6 |
|
| 1985 |
OKADA K, KOSEKI K, KITAHARA T, MORI K. Synthetic microbial chemistry. Part VII. Synthesis of the proposed structure of sclerosporin with a guaiane skeleton. Agricultural and Biological Chemistry. 49: 487-493. DOI: 10.1271/Bbb1961.49.487 |
0.629 |
|
| 1985 |
ABURATANI M, TAKEUCHI T, MORI K. Synthesis of brassinolide. Part I. Structural revision of the acetal intermediates in brassinolide synthesis. Agricultural and Biological Chemistry. 49: 3557-3562. DOI: 10.1271/Bbb1961.49.3557 |
0.428 |
|
| 1985 |
KATO M, MORI K. Synthesis of (3R,4S)-4-methyl-3 hexanol, the pheromone of the ant Tetramorium impurum. Agricultural and Biological Chemistry. 49: 3073-3075. DOI: 10.1271/Bbb1961.49.3073 |
0.444 |
|
| 1985 |
KATO M, MORI K. Pheromone synthesis. Part 76. Synthesis of the enantiomers of 14-methyl-1-octadecene, the sex pheromone of the peach leafminer moth. Agricultural and Biological Chemistry. 49: 2479-2480. DOI: 10.1271/Bbb1961.49.2479 |
0.45 |
|
| 1985 |
YANAI M, SUGAI T, MORI K. Carotenoids and degraded carotenoids. Part V. Synthesis of (S)-2-hydroxy-.BETA.-ionone, employing (S)-3-hydroxy-2,2-dimethylcyclohexanone as the chiral starting material. Agricultural and Biological Chemistry. 49: 2373-2377. DOI: 10.1271/Bbb1961.49.2373 |
0.35 |
|
| 1985 |
Aburatani M, Takeuchi T, Mori K. Structural Revision of the Acetal Intermediates in Brassinolide Synthesis Agricultural and Biological Chemistry. 49: 3557-3562. DOI: 10.1080/00021369.1985.10867278 |
0.406 |
|
| 1985 |
Yanai M, Sugai T, Mori K. Synthesis of (5)-2-hydroxy-/?-ionone, employing (5)-3-hydroxy-2,2-dimethylcyclohexanone as the chiral starting material Agricultural and Biological Chemistry. 49: 2373-2377. DOI: 10.1080/00021369.1985.10867072 |
0.399 |
|
| 1985 |
Mori K, Sugai T, Maeda Y, Okazaki T, Noguchi T, Naito H. Synthesis of the racemic and optically active forms of gizzerosine, the inducer of gizzard erosion in chicks Tetrahedron. 41: 5307-5311. DOI: 10.1016/S0040-4020(01)96782-1 |
0.403 |
|
| 1985 |
Mori K, Gupta AK. Chiral synthesis of (R)-( -)-mellein and (3R,4aS)-( + )-ramulosin Tetrahedron. 41: 5295-5299. DOI: 10.1016/S0040-4020(01)96780-8 |
0.36 |
|
| 1985 |
Mori K, Seu Y. Synthesis of both the enantiomers of endo-brevicomin, the aggregation pheromone of Dryocoetes autographus Tetrahedron. 41: 3429-3431. DOI: 10.1016/S0040-4020(01)96695-5 |
0.435 |
|
| 1985 |
Mori K, Watanabe H. A new synthesis of serricornin [(4s,6s,7s)-7-hydroxy-4,6-dimethyl-3-nonanone], the sex pheromone of the cigarette beetle Tetrahedron. 41: 3423-3428. DOI: 10.1016/S0040-4020(01)96694-3 |
0.649 |
|
| 1985 |
Mori K, Otsuka T. Simple synthesis of all of the four stereoisomers of 5-hydroxy-4-decanolide (l-factors), the proposed autoregulators from Tetrahedron. 41: 3253-3256. DOI: 10.1016/S0040-4020(01)96676-1 |
0.321 |
|
| 1985 |
Mori K, Takechi S. Synthesis of the natural enantiomers of ascochlorin, ascofuranone and ascofuranol Tetrahedron. 41: 3049-3062. DOI: 10.1016/S0040-4020(01)96657-8 |
0.429 |
|
| 1985 |
Mori K, Funaki Y. Synthesis of (4,8,2,3,2'--2'-hydroxyhexadecanoyl-1--β-D-glucopyranosyl-9-methyl-4,8-sphingadienine, the fruiting-inducing cerebroside in a basidiomycete Tetrahedron. 41: 2379-2386. DOI: 10.1016/S0040-4020(01)96633-5 |
0.383 |
|
| 1985 |
Mori K, Funaki Y. Synthesis of (4,8,2,3,2')--2' -hydroxyhexadecanoyl-9-methyl-4,8-sphingadiemine, the ceramide portion of the fruiting-inducing cerebroside in a basidiomycete , and its (2,3)-isomer Tetrahedron. 41: 2369-2377. DOI: 10.1016/S0040-4020(01)96632-3 |
0.405 |
|
| 1985 |
Mori K, Waku M, Sakakibara M. Synthesis of arnebinol, an ansa-type prenylated phenol with effects inhibitory to prostaglandin biosynthesis Tetrahedron. 41: 2825-2830. DOI: 10.1016/S0040-4020(01)96599-8 |
0.37 |
|
| 1985 |
Mori K, Okada K. Synthesis of mevalonolactone (hiochic acid lactone) employing asymmetric epoxidation as the key-step Tetrahedron. 41: 557-559. DOI: 10.1016/S0040-4020(01)96500-7 |
0.434 |
|
| 1985 |
Mori K, Otsuka T. Synthesis of (2S,3S)-2,3-octanediol and (S)-2-hydroxy-3-octanone, the male sex pheromone of the grape borer xylotrechus pyrrhoderus Tetrahedron. 41: 553-556. DOI: 10.1016/S0040-4020(01)96499-3 |
0.374 |
|
| 1985 |
Mori K, Otsuka T. Synthesis of the enantiomers of 5-hexadecanolide, the pheromone of the queen of the oriental hornet, vespa orientalis,employing enzymic resolution of (±)-2-aminotridecanoic acid as the key-step Tetrahedron. 41: 547-551. DOI: 10.1016/S0040-4020(01)96498-1 |
0.415 |
|
| 1985 |
Mori K, Senda S. Synthesis of the enantiomers of cis-2-methyl-5-hexanolide, the major component of the sex pheromone of the carpenter bee Tetrahedron. 41: 541-546. DOI: 10.1016/S0040-4020(01)96497-X |
0.427 |
|
| 1985 |
Mori K, Mori H, Sugai T. Biochemical preparations of both the enantiomers of methyl 3-hydroxypentanoate and their conversion to the enantiomers of 4-hexanolide, the pheromone of trogoderma glabrum Tetrahedron. 41: 919-925. DOI: 10.1016/S0040-4020(01)96410-5 |
0.358 |
|
| 1985 |
Mori K, Uematsu T, Yanagi K, Minobe M. Synthesis of the optically active forms of 4,10-dihydroxy-1,7-dioxaspiro[5.5]undecane and their conversion to the enantiomers of 1,7-dioxaspiro[5.5]undecane, the olive fly pheromone Tetrahedron. 41: 2751-2758. DOI: 10.1016/S0040-4020(01)96376-8 |
0.395 |
|
| 1985 |
Mori K, Watanabe H, Yanagi K, Minobe M. Synthesis of the enantiomers of 1,7-dioxaspiro[5.5]undecane, 4-hydroxy-1,7-dioxaspirol[5.5]undecane and 3-hydroxy-1,7-dioxaspiroi[5.5]undecane Tetrahedron. 41: 3663-3672. DOI: 10.1016/S0040-4020(01)91385-7 |
0.661 |
|
| 1985 |
Mori K, Waku M. Synthesis of oryzalexins a, b and c, the diterpenoidal phytoalexins isolated from rice blast leaves infected with pyricularia oryzae Tetrahedron. 41: 5653-5660. DOI: 10.1016/S0040-4020(01)91369-9 |
0.334 |
|
| 1985 |
Mori K, Mori H. Synthesis of (1,5)-karahana ether and (1,5)-karahana lactone, the optically active forms of unique monoterpenes wit Tetrahedron. 41: 5487-5493. DOI: 10.1016/S0040-4020(01)91348-1 |
0.436 |
|
| 1985 |
Kitahara T, Kurata H, Matsuoka T, Mori K. Synthesis of both the enantiomers of sclerosporin and sclerosporal, sporogenic substance of sclerotinia fructicola Tetrahedron. 41: 5475-5485. DOI: 10.1016/S0040-4020(01)91347-X |
0.646 |
|
| 1985 |
Laurence BR, Mori K, Otsuka T, Pickett JA, Wadhams LJ. Absolute configuration of mosquito oviposition attractant pheromone, 6-acetoxy-5-hexadecanolide Journal of Chemical Ecology. 11: 643-648. DOI: 10.1007/Bf00988573 |
0.386 |
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| 1985 |
Mori K, Soga H, Ikunaka M. Pheromone Syntheses, LXXVIII. Synthesis of the Four Thermodynamically Stable Stereoisomers of 2,7-Dimethyl-1,6-dioxaspiro[4.6]undecane, a Component of the Volatile Secretion from the Mandibular Glands ofAndrena haemorrhoa F. Liebigs Annalen Der Chemie. 1985: 2194-2205. DOI: 10.1002/Jlac.198519851109 |
0.379 |
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| 1985 |
Mori K, Kato M. Pheromone Syntheses, LXXVII. New Synthesis of the Enantiomers of 14-Methyl-1-octadecene, the Pheromone ofLyonetia clerkella L. Liebigs Annalen Der Chemie. 1985: 2083-2087. DOI: 10.1002/Jlac.198519851015 |
0.419 |
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| 1985 |
MORI K, WATANABE H, YANAGI K, MINOBE M. ChemInform Abstract: PHEROMONE SYNTHESIS. 79. SYNTHESIS OF THE ENANTIOMERS OF 1,7-DIOXASPIRO(5.5)UNDECANE, 4-HYDROXY-1,7-DIOXASPIRO(5.5)UNDECANE, AND 3-HYDROXY-1,7-DIOXASPIRO(5.5)UNDECANE, THE COMPONENTS OF THE OLIVE FRUIT FLY PHEROMONE Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198551339 |
0.683 |
|
| 1985 |
MORI K, SEU Y. ChemInform Abstract: PHEROMONE SYNTHESIS. PART 75. SYNTHESIS OF BOTH THE ENANTIOMERS OF ENDO-BREVICOMIN, THE AGGREGATION PHEROMONE OF DRYOCOETES AUTOGRAPHUS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198549330 |
0.438 |
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| 1985 |
MORI K, UEMATSU T, YANAGI K, MINOBE M. ChemInform Abstract: PHEROMONE SYNTHESIS. 74. SYNTHESIS OF THE OPTICALLY ACTIVE FORMS OF 4,10-DIHYDROXY-1,7-DIOXASPIRO(5.5)UNDECANE AND THEIR CONVERSION TO THE ENANTIOMERS OF 1,7-DIOXASPIRO(5.5)UNDECANE, THE OLIVE FLY PHEROMONE Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198541360 |
0.424 |
|
| 1985 |
Mori K, Kato M, Kuwahara S. Pheromone syntheses, LXXIII. New synthesis of (4R,8R)-4,8-dimethyldecanal, the aggregation pheromone oftribolium castaneum, and its (4R,8S)-isomer Liebigs Annalen Der Chemie. 1985: 861-865. DOI: 10.1002/Chin.198533377 |
0.386 |
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| 1984 |
SAKAKIBARA M, MORI K. Short-step syntheses of homodolicholide and homodolichosterone. Agricultural and Biological Chemistry. 48: 745-752. DOI: 10.1271/Bbb1961.48.745 |
0.367 |
|
| 1984 |
NNKAGAWA N, MORI K. Pheromone synthesis. Part 68. Synthesis of (3S,4S)-4-methyl-3-heptanol and its (3S,4R)-isomer employing asymmetric epoxidation coupled with regioselective cleavage of epoxides with trimethylaluminum. Agricultural and Biological Chemistry. 48: 2505-2510. DOI: 10.1271/bbb1961.48.2505 |
0.361 |
|
| 1984 |
SUGAI T, MORI K. Preparative bioorganic chemistry. Part V. Preparation of (R)-ibuprofen and related carboxylic acids using microbial oxidation of an aromatic hydrocarbon by Rhodococcus sp. BPM 1613. Agricultural and Biological Chemistry. 48: 2501-2504. DOI: 10.1271/Bbb1961.48.2501 |
0.36 |
|
| 1984 |
SUGAI T, MORI K. Pheromone synthesis. Part 67. Synthesis of both the enantiomers of 4-dodecanolide, a defensive secretion of rove beetles. Agricultural and Biological Chemistry. 48: 2497-2500. DOI: 10.1271/Bbb1961.48.2497 |
0.455 |
|
| 1984 |
KITAHARA T, IWAMOTO M, TAKAGI Y, MORI K, MATSUI M. Synthesis of medium- and marcro-cyclic compounds. Part III. Synthesis of jasmine ketolactone. Agricultural and Biological Chemistry. 48: 1731-1734. DOI: 10.1271/Bbb1961.48.1731 |
0.666 |
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| 1984 |
Nakagawa N, Mori K. New Syntheses of (R)-(+)-3-Acetoxy-2,6-dimethyl-l,5-heptadiene, the Pheromone of the Comstock Mealybug Agricultural and Biological Chemistry. 48: 2799-2803. DOI: 10.1080/00021369.1984.10866566 |
0.354 |
|
| 1984 |
Nakagawa N, Mori K. Synthesis of (3S,4S)-4-Methyl-3-heptanol and Its (3S,4R)-Isomer Employing Asymmetric Epoxidation Coupled with Regioselective Cleavage of Epoxides with Trimethylaluminum Agricultural and Biological Chemistry. 48: 2505-2510. DOI: 10.1080/00021369.1984.10866523 |
0.428 |
|
| 1984 |
Sugai T, Mori K. Synthesis of Both the Enantiomers of 4-Dodecanolide, a Defensive Secretion of Rove Beetles Agricultural and Biological Chemistry. 48: 2497-2500. DOI: 10.1080/00021369.1984.10866521 |
0.436 |
|
| 1984 |
Kitahara T, Matsuoka T, Katayama M, Marumo S, Mori K. Synthesis of the enantiomers of sclerosporin and sclerosporal to determine the absolute configuration of the natural products Tetrahedron Letters. 25: 4685-4688. DOI: 10.1016/S0040-4039(01)91234-1 |
0.631 |
|
| 1984 |
Mori K, Tamon U, Hidenori W, Kazunori Y, Masao M. Synthesis of the enantiomers of 1,7-dioxaspiro[5.5]undecane and 4-hydroxy 1,7-dioxaspiro[5.5]undecane, the components of the olive fly pheromone Tetrahedron Letters. 25: 3875-3878. DOI: 10.1016/S0040-4039(01)91192-X |
0.422 |
|
| 1984 |
Mori K, Watanabe H. Synthesis of the enantiomers of 3-hydroxy-1,7-dioxaspiro[5.5]undecane, a minor component of the olive fly pheromone Tetrahedron Letters. 25: 6025-6026. DOI: 10.1016/S0040-4039(01)81750-0 |
0.66 |
|
| 1984 |
Mori K, Funaki Y. Synthesis of (2s,3r,4e,8e)-n-(2′r)-2′-hydroxyhexadecanoyl-9-methyl-4,8-sphingadienine, the ceramide portion of the fruiting-inducing cerebroside in a basidiomycete schizophyllum commune Tetrahedron Letters. 25: 5291-5294. DOI: 10.1016/S0040-4039(01)81586-0 |
0.409 |
|
| 1984 |
Mori K, Sakakibara M, Waku M. Synthesis of arnebinol, an inhibitor of prostaglandin biosynthesis Tetrahedron Letters. 25: 1085-1086. DOI: 10.1016/S0040-4039(01)80108-8 |
0.358 |
|
| 1984 |
Mori K, Fujioka T. Synthesis of (±)-ascochlorin, (±)-ascofuranone and LL-Z1272 Tetrahedron. 40: 2711-2720. DOI: 10.1016/S0040-4020(01)96890-5 |
0.346 |
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| 1984 |
Mori K, Ikunaka M. Synthesis of all of the four energetically possible stereoisomers of 7-ethyl-2-methyl-1,6-dioxaspiro[4.5]decane Tetrahedron. 40: 3471-3479. DOI: 10.1016/S0040-4020(01)91498-X |
0.405 |
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