Year |
Citation |
Score |
2002 |
Hagiwara H, Kobayashi K, Miya S, Hoshi T, Suzuki T, Ando M, Okamoto T, Kobayashi M, Yamamoto I, Ohtsubo S, Kato M, Uda H. First total syntheses of the phytotoxins solanapyrones D and E via the domino Michael protocol. The Journal of Organic Chemistry. 67: 5969-76. PMID 12182630 DOI: 10.1021/Jo0163602 |
0.347 |
|
1997 |
Kosugi H, Hoshino K, Uda H. Highly enantiofacial protonation of prochiral lithium enolates with chiral β-hydroxy sulfoxides Tetrahedron Letters. 38: 6861-6864. DOI: 10.1016/S0040-4039(97)01618-3 |
0.345 |
|
1995 |
Hagiwara H, Nakano T, Kon-No M, Uda H. Total synthesis of (+)-compactin by a double Michael protocol Journal of the Chemical Society, Perkin Transactions 1. 777-783. DOI: 10.1039/P19950000777 |
0.387 |
|
1995 |
Hagiwara H, Inome K, Uda H. A total synthesis of an antibacterial clerodane, 16-hydroxycleroda-3,13(14) Z-dien-15,16-olide Journal of the Chemical Society, Perkin Transactions 1. 757-764. DOI: 10.1039/P19950000757 |
0.368 |
|
1995 |
Hagiwara H, Okamoto T, Harada N, Uda H. Double Michael reaction of Wieland-Miescher ketone Tetrahedron. 51: 9891-9898. DOI: 10.1016/0040-4020(95)00566-Q |
0.343 |
|
1994 |
Kosugi H, Hoshino K, Uda H. β-Hydroxy sulfoxide derivatives as a powerful chiral protonating reagent Phosphorus, Sulfur, and Silicon and the Related Elements. 95: 401-402. DOI: 10.1080/10426509408034251 |
0.346 |
|
1994 |
Hagiwara H, Kon-No M, Nakano T, Uda H. Total synthesis of (+)-dihydrocompactin Journal of the Chemical Society, Perkin Transactions 1. 2417-2430. DOI: 10.1039/P19940002417 |
0.397 |
|
1994 |
Harada N, Sugioka T, Uda H, Kuriki T, Kobayashi M, Kitagawa I. Total synthesis, absolute configuration, and later isolation of (-)-prehalenaquinone, a putative biosynthetic precursor to the marine natural products halenaquinone and xestoquinone Journal of Organic Chemistry. 59: 6606-6613. DOI: 10.1021/Jo00101A019 |
0.312 |
|
1994 |
Kosugi H, Kanno O, Uda H. Synthesis of enantiomerically pure juvenile hormone II Tetrahedron: Asymmetry. 5: 1139-1142. DOI: 10.1016/0957-4166(94)80140-1 |
0.351 |
|
1993 |
Hagiwara H, Nakano T, Uda H. Enzymatic Kinetic Resolution of 2-Cyclohexen-1-ol Derivatives Bulletin of the Chemical Society of Japan. 66: 3110-3112. DOI: 10.1246/Bcsj.66.3110 |
0.328 |
|
1993 |
Hagiwara H, Abe F, Uda H. Bicycloannulation of α-bromo α,β-unsaturated esters; synthesis of the tricyclo[4.4.0.01,5]decane framework and its congeners Journal of the Chemical Society, Perkin Transactions 1. 2651-2655. DOI: 10.1039/P19930002651 |
0.358 |
|
1993 |
Hagiwara H, Akama T, Okano A, Uda H. Annulation by sequential double Michael reaction; synthesis of decalones and its application to the syntheses of ε-cadinene, khusitone and khusilal Journal of the Chemical Society, Perkin Transactions 1. 2173-2184. DOI: 10.1039/P19930002173 |
0.394 |
|
1993 |
Harada N, Soutome T, Nehira T, Uda H, Oi S, Okamura A, Miyano S. Revision of the absolute configurations of [8]paracyclophane-10-carboxylic and 15-methyl[10]paracyclophane-12-carboxylic acids Journal of the American Chemical Society. 115: 7547-7548. DOI: 10.1021/Ja00069A082 |
0.34 |
|
1993 |
Harada N, Soutome T, Murai S, Uda H. A chiral probe useful for optical resolution and X-ray crystallographic determination of the absolute stereochemistry of carboxylic acids Tetrahedron: Asymmetry. 4: 1755-1758. DOI: 10.1016/S0957-4166(00)80409-7 |
0.314 |
|
1993 |
Kosugi H, Miura Y, Kanna H, Uda H. New route to enantiomerically pure 4,4-Disubstituted cyclohex-2-en-1-ones: Asymmetric synthesis of (+)-mesembrine Tetrahedron: Asymmetry. 4: 1409-1412. DOI: 10.1016/S0957-4166(00)80327-4 |
0.349 |
|
1992 |
Hagiwara H, Kimura K, Uda H. High diastereoselection in the aldol reaction of the bistrimethylsilyl enol ether of methyl acetoacetate with 2-benzyloxyhexanal: Synthesis of (-)-pestalotin Journal of the Chemical Society, Perkin Transactions 1. 693-700. DOI: 10.1039/P19920000693 |
0.402 |
|
1992 |
Kosugi H, Hoshino K, Uda H. Novel transformation of β-keto sulfoxides to unsaturated β-keto sulfides Journal of the Chemical Society, Chemical Communications. 560-561. DOI: 10.1039/C39920000560 |
0.328 |
|
1991 |
Kosugi H, Hoshino K, Uda H. Simple Synthesis and the Diels–Alder Reaction of 3-(p-Tolylthio)-2-(trimethylsilyloxy)-1,3-butadiene Chemistry Letters. 20: 1577-1578. DOI: 10.1246/Cl.1991.1577 |
0.317 |
|
1991 |
Hagiwara H, Uda H. Total synthesis and absolute stereostructure of (+)-dysideapalaunic acid Journal of the Chemical Society, Perkin Transactions 1. 1803-1807. DOI: 10.1039/P19910001803 |
0.32 |
|
1991 |
Harada N, Ono H, Nishiwaki T, Uda H. Synthesis, circular dichroism and absolute stereochemistry of chiral spiroaromatic compounds. 9,9′-Spirobifluorene derivatives Journal of the Chemical Society, Chemical Communications. 1753-1755. DOI: 10.1039/C39910001753 |
0.351 |
|
1991 |
Kosugi H, Hoshino K, Uda H. Cyclisation of polyenic β-keto suiphoxides. A novel route to optically active intermediates for cyclic terpenoid synthesis Journal of the Chemical Society, Chemical Communications. 1173-1174. DOI: 10.1039/C39910001173 |
0.321 |
|
1991 |
Hagiwara H, Abe F, Uda H. Bicycloannulation leading to the tricyclo[4.4.0.01,5]decane framework and its congeners Journal of the Chemical Society, Chemical Communications. 1070-1071. DOI: 10.1039/C39910001070 |
0.36 |
|
1990 |
Inoue Y, Ohuchi K, Imaizumi S, Hagiwara H, Uda H. New Syntheses of Geiparvarin and 2,5-Dimethyl-3(2H)-furanone Via Co2 Mediated Bond Reorganization Synthetic Communications. 20: 3063-3068. DOI: 10.1080/00397919008051526 |
0.309 |
|
1990 |
Harada N, Sugioka T, Uda H, Kuriki T. Efficient Preparation of Optically Pure Wieland-Miescher Ketone and Confirmation of Its Absolute Stereochemistry by the CD Exciton Chirality Method Synthesis. 1: 53-56. DOI: 10.1055/S-1990-26786 |
0.371 |
|
1990 |
Hagiwara H, Okano A, Uda H. One-pot annulation to tricyclo[5.3.1.03,8]undecane-2,6-diones by sequential three-fold Michael reactions. A formal synthesis of (±)-seychellene Journal of the Chemical Society, Perkin Transactions 1. 2109-2113. DOI: 10.1039/P19900002109 |
0.361 |
|
1990 |
Hagiwara H, Uda H. Total synthesis of (+)-perrottetianal A Journal of the Chemical Society, Perkin Transactions 1. 1901-1908. DOI: 10.1039/P19900001901 |
0.369 |
|
1990 |
Harada N, Sugioka T, Uda H, Kuriki T. Total synthesis and absolute stereochemistry of (+)-xestoquinone and xestoquinol Journal of Organic Chemistry. 55: 3158-3163. DOI: 10.1021/Jo00297A035 |
0.309 |
|
1989 |
Hagiwara H, Akama T, Okano A, Uda H. Asymmetric Two-Fold Michael Reaction. Synthesis of Optically Active 4-Substituted 1-Decalones from Trimethylsilyl Enol Ether of 1-Acetylcyclohexene Chemistry Letters. 18: 2149-2152. DOI: 10.1246/Cl.1989.2149 |
0.421 |
|
1989 |
Kosugi H, Watanabe Y, Uda H. Lewis acid-mediated carbon-carbon bond forming reaction using the pummerer rearrangement products from chiral β-hydroxy sulfoxides Chemistry Letters. 18: 1865-1868. DOI: 10.1246/Cl.1989.1865 |
0.378 |
|
1989 |
Hagiwara H, Uda H. A Total Synthesis of (−)-Sacculatal Bulletin of the Chemical Society of Japan. 62: 624-626. DOI: 10.1246/Bcsj.62.624 |
0.318 |
|
1989 |
Kosugi H, Tagami K, Takahashi A, Kanna H, Uda H. Highly enantiospecific synthesis of 4-alkyl and 4,5-dialkyl substituted 4,5-dihydrofuran-2(3H)-ones from optically active (E)- and (Z)-alk-1-enyl p-tolyl sulphoxides: Application to the synthesis of lignan lactones Journal of the Chemical Society, Perkin Transactions 1. 935-943. DOI: 10.1039/P19890000935 |
0.414 |
|
1988 |
Hagiwara H, Akama T, Okano A, Uda H. Synthesis of Substituted 2-Decalones from 1-Acetylcyclohexenes and α-Trimethylsilyl α,β-Unsaturated Carbonyl Compounds by Two-Fold Michael Reactions. Synthesis of (±)-Khusitone Chemistry Letters. 17: 1793-1796. DOI: 10.1246/Cl.1988.1793 |
0.383 |
|
1988 |
Hagiwara H, Uda H. Total synthesis of (+)-dysideapalaunic acid Journal of the Chemical Society, Chemical Communications. 815-817. DOI: 10.1039/C39880000815 |
0.335 |
|
1988 |
Harada N, Sugioka T, Ando Y, Uda H, Kuriki T. Total synthesis of (+)-halenaquinol and (+)-halenaquinone. Experimental proof of their absolute stereostructures theoretically determined Journal of the American Chemical Society. 110: 8483-8487. DOI: 10.1021/Ja00233A026 |
0.314 |
|
1987 |
Hagiwara H, Okano A, Akama T, Uda H. Lewis acid assisted annelation of trimethylsilyl enol ethers of 1-acetylcyclohexenes with α,β-unsaturated carbonyl compounds to give substituted 2-decalones; synthesis of (±)-ε-cadinene Journal of the Chemical Society, Chemical Communications. 1333-1335. DOI: 10.1039/C39870001333 |
0.397 |
|
1986 |
Tamai Y, Hagiwara H, Uda H. A total synthesis of (+)-pisiferol Journal of the Chemical Society-Perkin Transactions 1. 1311-1315. DOI: 10.1039/P19860001311 |
0.425 |
|
1986 |
Hagiwara H, Uda H. A synthesis of functionalised tricyclo[5.2.2.0]undecenes related to the isoeremolactone skeleton Journal of the Chemical Society-Perkin Transactions 1. 17: 629-632. DOI: 10.1039/P19860000629 |
0.396 |
|
1986 |
Kosugi H, Kitaoka M, Takahashi A, Uda H. Highly enantioselective rearrangement of (S)-E-α-p-tolysulphinyl-α,β-enoates to (R)-E-γ-hydroxy-α,β-enoates Journal of the Chemical Society, Chemical Communications. 1268-1270. DOI: 10.1039/C39860001268 |
0.318 |
|
1986 |
Hagiwara H, Kimura K, Uda H. Highly diastereoselective titanium tetrachloride-mediated aldol condensation of the bistrimethylsilyl enol ether of acetoacetic ester with 2-benzyloxyhexanal. A synthesis of (–)-pestalotin Journal of the Chemical Society, Chemical Communications. 860-861. DOI: 10.1039/C39860000860 |
0.412 |
|
1986 |
Okada K, Samizo F, Oda M, Harada N, Uda H. Absolute stereochemistries of -2,3-disubstituted spirocyclopropane-1,9′-fluorene derivatives: A styryl modification cd-method for carboxyl substituted chiral centers Tetrahedron Letters. 27: 4493-4496. DOI: 10.1016/S0040-4039(00)84987-4 |
0.348 |
|
1986 |
Tamai Y, Hagiwara H, Uda H. Total Synthesis of (+)‐Pisiferol (XII). Cheminform. 17. DOI: 10.1002/Chin.198647347 |
0.321 |
|
1985 |
Harada N, Iwabuchi J, Yokota Y, Uda H, Okamoto Y, Yuki H, Kawada Y. Liquid chromatographic optical resolution of 2,2'-spirobibenz[e]indan derivatives and absolute stereochemistry as determined by the C.D. exciton chirality method Journal of the Chemical Society-Perkin Transactions 1. 16: 1845-1848. DOI: 10.1039/P19850001845 |
0.314 |
|
1985 |
Hagiwara H, Uda H. A stereoselective synthesis of (±)-malyngolide Journal of the Chemical Society-Perkin Transactions 1. 16: 1157-1159. DOI: 10.1039/P19850001157 |
0.326 |
|
1985 |
Hagiwara H, Uda H. A facile synthesis of 5-methyl-6,8-dioxabicyclo[3.2.1]octan-3-ones from 4-(t-butyldimethylsiloxy)pent-3-en-2-one and protected α-ketols. A synthesis of (±)-frontalin Journal of the Chemical Society-Perkin Transactions 1. 16: 283-287. DOI: 10.1039/P19850000283 |
0.405 |
|
1985 |
Hagiwara H, Okano A, Uda H. One-step synthesis of tricyclo[5.3.1.03,8]undecan-4,11-diones by three consecutive Michael reactions. A formal synthesis of (±)-seychellene Journal of the Chemical Society, Chemical Communications. 1047-1047. DOI: 10.1039/C39850001047 |
0.365 |
|
1985 |
Kosugi H, Konta H, Uda H. Highly diastereoselective reduction of chiral β-ketosulphoxides under chelation control: application to the synthesis of (R)-(+)-n-hexadecano-1,5-lactone Journal of the Chemical Society, Chemical Communications. 211-213. DOI: 10.1039/C39850000211 |
0.368 |
|
1985 |
Hagiwara H, Okano A, Uda H. One-Step Synthesis Of Tricyclo(5.3.1.03,8)Undecane-4,11-Diones By Three Consecutive Michael Reactions. A Formal Synthesis Of (.+-.)-Seychellene Cheminform. 16. DOI: 10.1002/Chin.198548147 |
0.376 |
|
1985 |
Tamai Y, Mizutani Y, Hagiwara H, Uda H, Harada N. Synthesis And Absolute Stereochemistry Of Optically Active Wieland-Miescher Ketone Analogs Bearing An Angular Protected Hydroxymethyl Group Cheminform. 16. DOI: 10.1002/Chin.198538196 |
0.328 |
|
1985 |
Kosugi H, Konta H, Uda H. HIGHLY DIASTEREOSELECTIVE REDUCTION OF CHIRAL β-KETO SULFOXIDES UNDER CHELATION CONTROL: APPLICATION TO THE SYNTHESIS OF (R)-(+)-N-HEXADECANO-1,5-LACTONE Cheminform. 16. DOI: 10.1002/Chin.198525118 |
0.341 |
|
1985 |
Hoshi N, Sato K, Uda H, Hagiwara H. Photochemistry Of 3-Alkylated And 3-Phenylated Oxepin-2(3H)-One Derivatives Cheminform. 16. DOI: 10.1002/Chin.198524105 |
0.331 |
|
1985 |
Harada N, Kohori J, Uda H, Nakanishi K, Takeda R. Absolute stereochemistry of (+)-1,8a-dihydro-3,8-dimethylazulene, a labile biosynthetic intermediate for 1,4-dimethylazulene. Determination by theoretical calculation of CD spectra and verification by synthesis of model compounds Journal of the American Chemical Society. 107: 423-428. DOI: 10.1002/Chin.198521316 |
0.45 |
|
1984 |
Hagiwara H, Sugioka T, Uda H. Dialkyl-Substituted Maleates from α-Bromoesters Synthetic Communications. 14: 1193-1198. DOI: 10.1080/00397918408076799 |
0.338 |
|
1984 |
Hagiwara H, Uda H. New route for synthesis of furan derivatives from protected α-ketols and ketones. A total synthesis of furoventalene Journal of the Chemical Society-Perkin Transactions 1. 15: 91-94. DOI: 10.1039/P19840000091 |
0.419 |
|
1984 |
Kitaoka M, Takahashi Y, Kosugi H, Uda H. Generation And Reactions Of The Allylic Carbanion Species From 2-Methyl-3-(Phenylthio)Propenoic Acid Derivatives Cheminform. 15. DOI: 10.1002/Chin.198401174 |
0.345 |
|
1983 |
Kitaoka M, Takahashi Y, Kosugi H, Uda H. Generation And Reactions Of The Allylic Carbanion Species From 2-Methyl-3-(Phenylthio)Propenoic Acid Derivatives Chemistry Letters. 12: 1065-1068. DOI: 10.1246/Cl.1983.1065 |
0.327 |
|
1983 |
Tamai Y, Mizutani Y, Uda H, Harada N. The absolute stereochemistry of Wieland–Miescher ketone analogues bearing an angular protected hydroxymethyl group Journal of the Chemical Society, Chemical Communications. 114-116. DOI: 10.1039/C39830000114 |
0.385 |
|
1982 |
Tamai Y, Hagiwara H, Uda H. Synthesis of Wieland–Miescher ketone analogues bearing an angular protected hydroxymethyl group Journal of the Chemical Society, Chemical Communications. 502-503. DOI: 10.1039/C39820000502 |
0.375 |
|
1982 |
Takahashi Y, Kosugi H, Uda H. A total synthesis of methylenomycin B Journal of the Chemical Society, Chemical Communications. 496-497. DOI: 10.1039/C39820000496 |
0.37 |
|
1982 |
Harada N, Ai T, Uda H. Absolute stereochemistry of 2,2′-spirobi-indane-1,1′-diols as determined by the C.D. exciton chirality method Journal of the Chemical Society, Chemical Communications. 232-233. DOI: 10.1039/C39820000232 |
0.327 |
|
1982 |
Tamai Y, Hagiwara H, Uda H. Synthesis Of Wieland-Miescher Ketone Analogs Bearing An Angular Protected Hydroxymethyl Group Cheminform. 13. DOI: 10.1002/Chin.198237178 |
0.339 |
|
1981 |
Takahashi Y, Isobe K, Hagiwara H, Kosugi H, Uda H. A total synthesis of (±)-methylenomycin A Journal of the Chemical Society, Chemical Communications. 714-715. DOI: 10.1039/C39810000714 |
0.351 |
|
1981 |
Harada N, Iwabuchi J, Yokota Y, Uda H, Nakanishi K. A chiroptical method for determining the absolute configuration of allylic alcohols Journal of the American Chemical Society. 103: 5590-5591. DOI: 10.1002/Chin.198150097 |
0.389 |
|
1981 |
Takahashi Y, Hagiwara H, Uda H, Kosugi H. A Facile Synthesis Of 4-Phenylthio-2(5H)-Furanone Derivatives. Synthesis Of Sesquirose Furan And Bullatenone Cheminform. 12: 225. DOI: 10.1002/Chin.198120192 |
0.314 |
|
1981 |
Kawamoto A, Uda H, Harada N. Acid-Catalyzed Rearrangement Of The Exo-1,2-Dioxetane Derivative From 1-Isopropylidene-4,4-Diphenyl-2,5-Cyclohexadiene Cheminform. 12. DOI: 10.1002/Chin.198107125 |
0.343 |
|
1980 |
Hoshi N, Furukawa Y, Hagiwara H, Uda H, Sato K. Enantiomer Differentiation In The Photoinduced 1,5-Phenyl Shift Of 3-Methyl-3-Phenyl-2(3H)-Oxepinone Utilizing Chiral Sensitizers Chemistry Letters. 9: 47-50. DOI: 10.1246/Cl.1980.47 |
0.365 |
|
1980 |
Kawamoto A, Uda H, Harada N. Acid-catalyzed rearrangement of the exo-1,2-dioxetane derivative from 1-isopropylidene-4,4-diphenyl-2,5-cyclohexadiene. Bulletin of the Chemical Society of Japan. 53: 3279-3283. DOI: 10.1246/Bcsj.53.3279 |
0.352 |
|
1980 |
Hagiwara H, Uda H, Kodama T. Synthetic study on several eremophilane sesquiterpenes using a common intermediate Journal of the Chemical Society-Perkin Transactions 1. 11: 963-977. DOI: 10.1039/P19800000963 |
0.344 |
|
1980 |
Yamada T, Hagiwara H, Uda H. Synthesis of 4-substituted 2-methyltetronic acid derivatives Journal of the Chemical Society, Chemical Communications. 838-839. DOI: 10.1039/C39800000838 |
0.402 |
|
1980 |
Yamada T, Hagiwara H, Uda H. Synthesis Of 4-Substituted 2-Methyltetronic Acid Derivatives Cheminform. 11. DOI: 10.1002/Chin.198052223 |
0.376 |
|
1980 |
Hoshi N, Furukawa Y, Hagiwara H, Uda H, Sato K. Enantiomer Differentiation In The Photoinduced 1,5-Phenyl Shift Of 3-Methyl-3-Phenyl-2(3H)-Oxepinone Utilizing Chiral Sensitizers Cheminform. 11. DOI: 10.1002/Chin.198045204 |
0.359 |
|
1980 |
Hoshi N, Hagiwara H, Uda H. Evidence For The Photolytic Reaction Pathway Of 3-Phenyl-2(3H)-Oxepinones. Synthesis, Reaction, And Isolation Of 7-Phenyl-2(7H)-Oxepinones Cheminform. 11. DOI: 10.1002/Chin.198015282 |
0.33 |
|
1980 |
Isobe K, Fuse M, Kosugi H, Hagiwara H, Uda H. Methyl 3‐Lithio‐2‐Methyl‐3‐Phenylthio‐2‐Propenoate As A Zwitterionic Three‐Carbon Addend; Reactions With Carbonyl Compounds Cheminform. 11. DOI: 10.1002/Chin.198007117 |
0.335 |
|
1979 |
Isobe K, Fuse M, Kosugi H, Hagiwara H, Uda H. Methyl 3-lithio-2-methyl-3-phenylthio-2-propenoate as a zwitterionic three-carbon addend; reactions with carbonyl compounds. Chemistry Letters. 8: 785-788. DOI: 10.1246/Cl.1979.785 |
0.386 |
|
1979 |
Hoshi N, Hagiwara H, Uda H. Evidence For The Photolytic Reaction Pathway Of 3-Phenyl-2(3H)-Oxepinones. Synthesis, Reaction, And Isolation Of 7-Phenyl-2(7H)-Oxepinones Chemistry Letters. 8: 1295-1298. DOI: 10.1246/Cl.1979.1295 |
0.362 |
|
1979 |
Yamagiwa S, Sato H, Hoshi N, Kosugi H, Uda H. New rearrangement reactions of α-phenylsulphinylacrylate derivatives Journal of the Chemical Society-Perkin Transactions 1. 10: 570-583. DOI: 10.1039/P19790000570 |
0.375 |
|
1978 |
Yamagiwa S, Kosugi H, Uda H. Synthesis of the Monoterpene Lactone from Chrysanthemum flosculosum L. Bulletin of the Chemical Society of Japan. 51: 3011-3015. DOI: 10.1246/Bcsj.51.3011 |
0.376 |
|
1978 |
Harada N, Takuma Y, Uda H. Synthesis and Absolute Stereochemistry of (+)-7,14-Dihydro-7,14-ethanodibenz[a,h]anthracene and Its Derivatives Bulletin of the Chemical Society of Japan. 51: 265-270. DOI: 10.1246/Bcsj.51.265 |
0.321 |
|
1978 |
Kosugi H, Uda H. Studies Directed Towards The Synthesis Of Fomannosin. A Synthesis Of (.+‐.)‐Dihydrofomannosin Acetate Cheminform. 9. DOI: 10.1002/Chin.197823312 |
0.37 |
|
1978 |
Harada N, Takuma Y, Uda H. Synthesis And Absolute Stereochemistry Of (+)-7,14-Dihydro-7,14-Ethanodibenz(A,H)Anthracene And Its Derivatives Cheminform. 9. DOI: 10.1002/Chin.197815182 |
0.372 |
|
1978 |
Sato K, Hagiwara H, Uda H. Reverse Di-Π-Methane Rearrangement. Minor Products Of Photolysis Of 3-Methyl-3-Phenyl-2(3H)-Oxepinone Cheminform. 9. DOI: 10.1002/Chin.197805125 |
0.334 |
|
1977 |
Sato K, Hagiwara H, Uda H. REVERSE DI-π-METHANE REARRANGEMENT. MINOR PRODUCTS OF PHOTOLYSIS OF 3-METHYL-3-PHENYL-2(3H)-OXEPINONE Chemistry Letters. 6: 175-178. DOI: 10.1246/Cl.1977.175 |
0.347 |
|
1977 |
Kosugi H, Uda H. Studies Directed Towards The Synthesis Of Fomannosin. A Synthesis Of (±)-Dihydrofomannosin Acetate Chemistry Letters. 6: 1491-1494. DOI: 10.1246/Cl.1977.1491 |
0.358 |
|
1977 |
Iwai K, Kosugi H, Uda H, Kawai M. New Method for Synthesis of Various Types of Substituted 2(5H)-Furanones Bulletin of the Chemical Society of Japan. 50: 242-247. DOI: 10.1246/Bcsj.50.242 |
0.408 |
|
1977 |
Harada N, Takuma Y, Uda H. Synthesis and absolute stereochemistry of (+)-6,15-dihydro-6,15-ethanonaphtho[2,3-c]pentaphene as determined by exciton chirality and X-ray Bijvoet methods. Bulletin of the Chemical Society of Japan. 50: 2033-2038. DOI: 10.1246/Bcsj.50.2033 |
0.313 |
|
1977 |
Harada N, Ochiai N, Takada K, Uda H. (1S,5S,6R) absolute stereochemistry of (-)-cis,trans-spiro[4·4] nonane-1,6-diyl bis(p-dimethylaminobenzoate) as determined by the exciton chirality method Journal of the Chemical Society, Chemical Communications. 495-497. DOI: 10.1039/C39770000495 |
0.305 |
|
1977 |
Harada N, Takuma Y, Uda H. Synthesis And Absolute Stereochemistry Of (+)-6,15-Dihydro-6,15-Ethanonaphtho(2,3-C)Pentaphene As Determined By Exciton Chirality And X-Ray Bijvoet Methods Cheminform. 8. DOI: 10.1002/Chin.197744216 |
0.315 |
|
1977 |
Iwai K, Kosugi H, Uda H, Kawai M. New Method For Synthesis Of Various Types Of Substituted 2(5H)-Furanones Cheminform. 8. DOI: 10.1002/Chin.197715181 |
0.346 |
|
1976 |
Kosugi H, Sekiguchi S, Sekita R, Uda H. Photochemical Cycloaddition Reactions of α,β-Unsaturated Lactones with Olefins, and Application to Synthesis of Natural Products Bulletin of the Chemical Society of Japan. 49: 520-528. DOI: 10.1246/Bcsj.49.520 |
0.369 |
|
1976 |
Hagiwara H, Kodama T, Kosugi H, Uda H. Methyl α-bromocrotonate as a biannelating agent; reactions with cyclohex-2-enones Journal of the Chemical Society, Chemical Communications. 413-413. DOI: 10.1039/C39760000413 |
0.391 |
|
1976 |
Kosugi H, Uda H, Yamagiwa S. Additive Pummerer rearrangement of methyl cyclopentylidene(phenylsulphinyl)-acetate induced by acetyl chloride, trifluoroacetic anhydride, or thionyl chloride Journal of the Chemical Society, Chemical Communications. 71-72. DOI: 10.1039/C39760000071 |
0.344 |
|
1976 |
Hagiwara H, Kodama T, Kosugi H, Uda H. METHYL α-BROMOCROTONATE AS A BIANNULATING AGENT, REACTIONS WITH CYCLOHEX-2-ENONES Cheminform. 7. DOI: 10.1002/Chin.197639201 |
0.344 |
|
1976 |
Kosugi H, Sekiguchi S, Sekita R, Uda H. PHOTOCHEMICAL CYCLOADDITION REACTIONS OF α,β-UNSATURATED LACTONES WITH OLEFINS, AND APPLICATION TO SYNTHESIS OF NATURAL PRODUCTS Cheminform. 7. DOI: 10.1002/Chin.197620094 |
0.364 |
|
1976 |
Kosugi H, Uda H, Yamagiwa S. Additive Pummerer Rearrangement Of Methyl Cyclopentylidene(Phenylsulphinyl)Acetate Induced By Acetyl Chloride, Trifluoroacetic Anhydride, Or Thionyl Chloride Cheminform. 7. DOI: 10.1002/Chin.197618107 |
0.333 |
|
1976 |
Hagiwara H, Miyashita M, Uda H, Yoshikoshi A. An Alternative Synthesis Of (+)-1,7-Dimethyl-4-Endo-Isopropyl-8-Syn-(2-Hydroxyethyl)Bicyclo(3.2.1)Oct-6-Ene, The Key Intermediate For The Synthesis Of (+)-Sativene And (+)-Cyclosativene Cheminform. 7. DOI: 10.1002/Chin.197611164 |
0.394 |
|
1976 |
Hagiwara H, Nakayama K, Uda H. MICHAEL REACTIONS OF α-PHENYLTHIO AND α-PHENYLSULFINYL CROTONIC ESTERS WITH CYCLIC ENONES Cheminform. 7. DOI: 10.1002/Chin.197611084 |
0.331 |
|
1975 |
Hagiwara H, Nakayama K, Uda H. Michael Reactions of α-Phenylthio and α-Phenyisulfinyl Crotonic Esters with Cyclic Enones Bulletin of the Chemical Society of Japan. 48: 3769-3770. DOI: 10.1246/Bcsj.48.3769 |
0.351 |
|
1975 |
Hagiwara H, Miyashita M, Uda H, Yoshikoshi A. An alternative synthesis of (+)-1,7-dimethyl-4-endo-isopropyl-8-syn-(2-hydroxyethyl)bicyclo(3.2.1)oct-6-ene, the key intermediate for the synthesis of (+)-sativene and (+)-cyclosativene. Bulletin of the Chemical Society of Japan. 48: 3723-3726. DOI: 10.1246/Bcsj.48.3723 |
0.388 |
|
1975 |
Kosugi H, Uda H, Yamagiwa S. Vinylogous Pummerer rearrangement of methyl cyclopentylidene(phenylsulphinyl)acetate Journal of the Chemical Society, Chemical Communications. 192-193. DOI: 10.1039/C39750000192 |
0.313 |
|
1975 |
Iwai K, Kawai M, Yamagiwa S, Kosugi H, Uda H. A New Synthetic Method for 2(5H)-Furanone Derivatives. Cheminform. 3: 1136. DOI: 10.1002/Chin.197620206 |
0.304 |
|
1975 |
Kosugi H, Uda H, Yamagiwa S. Vinylogous Pummerer Rearrangement Of Methyl Cyclopentylidene(Phenylsulphinyl)Acetate Cheminform. 6. DOI: 10.1002/Chin.197524256 |
0.322 |
|
1974 |
Iwai K, Kawai M, Kosugi H, Uda H. A NEW SYNTHETIC METHOD FOR γ-SUBSTITUTED Δα,β-BUTENOLIDES Chemistry Letters. 3: 385-388. DOI: 10.1246/Cl.1974.385 |
0.369 |
|
1972 |
Kawamoto A, Kosugi H, Uda H. 2(7H)-Oxepinones: Photochemical Oxidation Of 6-Monosubstituted Fulvenes Chemistry Letters. 1: 807-810. DOI: 10.1246/Cl.1972.807 |
0.317 |
|
1972 |
Harada N, Suzuki S, Uda H, Nakanishi K. CIRCULAR DICHROISM STUDIES OF DIMERIC FUNGAL PIGMENTS,(−)-LUTEOSKYRIN AND (+)-RUGULOSIN Chemistry Letters. 1: 67-70. DOI: 10.1246/Cl.1972.67 |
0.417 |
|
1972 |
Harada N, Uda H, Ueno H. Solvent Dependence In The Photochemical Oxidation Of 6,6-Dimethylfulvene And Isolation Of 5-Isopropenyl-4-Hydroxy-2-Cyclopentenone Chemistry Letters. 1: 663-666. DOI: 10.1246/Cl.1972.663 |
0.317 |
|
1972 |
Kido F, Uda H, Yoshikoshi A. Synthetic study on zizaane-type sesquiterpenoids Journal of the Chemical Society, Perkin Transactions 1. 1755-1760. DOI: 10.1039/P19720001755 |
0.402 |
|
1972 |
Tanaka A, Tanaka R, Uda H, Yoshikoshi A. Synthesis of cubebane-type sesquiterpenoids and the stereochemistry of cubebol Journal of the Chemical Society, Perkin Transactions 1. 1721-1727. DOI: 10.1039/P19720001721 |
0.427 |
|
1969 |
Kido F, Uda H, Yoshikoshi A. Total synthesis of zizaane-type sesquiterpenoids Journal of the Chemical Society D: Chemical Communications. 1335-1336. DOI: 10.1039/C29690001335 |
0.308 |
|
1969 |
Tanaka A, Uda H, Yoshikoshi A. Total synthesis of α-cubebene, β-cubebene, and cubebol Journal of the Chemical Society D: Chemical Communications. 308. DOI: 10.1039/C29690000308 |
0.326 |
|
1968 |
Tanaka A, Uda H, Yoshikoshi A. Synthesis of (±)-α-chamigrene Chemical Communications (London). 56-57. DOI: 10.1039/C19680000056 |
0.31 |
|
1966 |
Kurosawa K, Obara H, Uda H. Syntheses of dl-Tetrahydroanhydrodesoxyaucubigenin and Related Compounds Bulletin of the Chemical Society of Japan. 39: 530-535. DOI: 10.1246/Bcsj.39.530 |
0.353 |
|
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