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Yoshito Kishi - Publications

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
synthesis of natural products
Website:
http://www.chem.harvard.edu/research/faculty/yoshito_kishi.php
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162 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Praveen Kumar V, Kishi Y. Total Synthesis of Halistatins 1 and 2. Journal of the American Chemical Society. 142: 14743-14749. PMID 32786216 DOI: 10.1021/Jacs.0C07390  0.367
2017 Yahata K, Ye N, Iso K, Ai Y, Lee J, Kishi Y. Stereocontrolled Synthesis of Left Halves of Halichondrins. The Journal of Organic Chemistry. PMID 28741354 DOI: 10.1021/Acs.Joc.7B01284  0.506
2017 Yahata K, Ye N, Iso K, Naini SR, Yamashita S, Ai Y, Kishi Y. Unified Synthesis of Right Halves of Halichondrins A-C. The Journal of Organic Chemistry. PMID 28741352 DOI: 10.1021/Acs.Joc.7B01283  0.787
2017 Kishi Y, Yahata K, Ye N, Ai Y, Iso K. Unified, Efficient, and Scalable Synthesis of Halichondrins, with Use of Zr/Ni-Mediated One-Pot Ketone Synthesis as Final Coupling Reaction. Angewandte Chemie (International Ed. in English). PMID 28683187 DOI: 10.1002/Ange.201705523  0.555
2017 Kishi Y, Ai Y, Ye N, Wang Q, Yahata K. Zr/Ni-Mediated One-Pot Ketone Synthesis. Angewandte Chemie (International Ed. in English). PMID 28683181 DOI: 10.1002/Ange.201705520  0.489
2017 Kumar VP, Babu VS, Yahata K, Kishi Y. Fe/Cu-Mediated One-Pot Ketone Synthesis. Organic Letters. PMID 28489396 DOI: 10.1021/Acs.Orglett.7B01128  0.324
2016 Lee JH, Li Z, Osawa A, Kishi Y. Extension of Pd-Mediated One-Pot Ketone Synthesis to Macrocyclization: Application to a New Convergent Synthesis of Eribulin. Journal of the American Chemical Society. PMID 27936750 DOI: 10.1021/Jacs.6B11663  0.343
2015 Wadagni A, Frimpong M, Phanzu DM, Ablordey A, Kacou E, Gbedevi M, Marion E, Xing Y, Babu VS, Phillips RO, Wansbrough-Jones M, Kishi Y, Asiedu K. Simple, Rapid Mycobacterium ulcerans Disease Diagnosis from Clinical Samples by Fluorescence of Mycolactone on Thin Layer Chromatography. Plos Neglected Tropical Diseases. 9: e0004247. PMID 26583925 DOI: 10.1371/Journal.Pntd.0004247  0.577
2015 Converse PJ, Tyagi S, Xing Y, Li SY, Kishi Y, Adamson J, Nuermberger EL, Grosset JH. Efficacy of Rifampin Plus Clofazimine in a Murine Model of Mycobacterium ulcerans Disease. Plos Neglected Tropical Diseases. 9: e0003823. PMID 26042792 DOI: 10.1371/Journal.Pntd.0003823  0.576
2015 Li J, Yan W, Kishi Y. Unified Synthesis of C1-C19 Building Blocks of Halichondrins via Selective Activation/Coupling of Polyhalogenated Nucleophiles in (Ni)/Cr-Mediated Reactions. Journal of the American Chemical Society. 137: 6226-31. PMID 25923790 DOI: 10.1021/Jacs.5B03499  0.535
2015 Yan W, Li Z, Kishi Y. Selective activation/coupling of polyhalogenated nucleophiles in ni/cr-mediated reactions: synthesis of c1-c19 building block of halichondrin bs. Journal of the American Chemical Society. 137: 6219-25. PMID 25923602 DOI: 10.1021/Jacs.5B03498  0.323
2015 Kishi Y, Goto T, Hirata Y, Shimomura O, Johnson FH. The structure of Cypridina luciferin Bioluminescence in Progress. 89-113. DOI: 10.1016/S0040-4039(01)82760-X  0.516
2015 Li X, Babu VS, Kishi Y. Stereoselective total synthesis and stereochemistry confirmation of photo-mycolactones Tetrahedron Letters. 56: 3220-3224. DOI: 10.1016/J.Tetlet.2014.12.024  0.35
2014 Ueda A, Yamamoto A, Kato D, Kishi Y. Total synthesis of halichondrin A, the missing member in the halichondrin class of natural products. Journal of the American Chemical Society. 136: 5171-6. PMID 24606005 DOI: 10.1021/Ja5013307  0.397
2014 Converse PJ, Xing Y, Kim KH, Tyagi S, Li SY, Almeida DV, Nuermberger EL, Grosset JH, Kishi Y. Accelerated detection of mycolactone production and response to antibiotic treatment in a mouse model of Mycobacterium ulcerans disease. Plos Neglected Tropical Diseases. 8: e2618. PMID 24392174 DOI: 10.1371/Journal.Pntd.0002618  0.597
2012 Xing Y, Hande SM, Kishi Y. Photochemistry of mycolactone A/B, the causative toxin of Buruli ulcer. Journal of the American Chemical Society. 134: 19234-9. PMID 23121070 DOI: 10.1021/Ja309215M  0.617
2012 Liu X, Li X, Chen Y, Hu Y, Kishi Y. On Ni catalysts for catalytic, asymmetric Ni/Cr-mediated coupling reactions. Journal of the American Chemical Society. 134: 6136-9. PMID 22443690 DOI: 10.1021/Ja302177Z  0.31
2012 Shan M, Kishi Y. Concise and highly stereoselective synthesis of the C20-C26 building block of halichondrins and Eribulin. Organic Letters. 14: 660-3. PMID 22236198 DOI: 10.1021/Ol203373D  0.389
2012 Yamamoto A, Ueda A, Brémond P, Tiseni PS, Kishi Y. Total synthesis of halichondrin C. Journal of the American Chemical Society. 134: 893-6. PMID 22188422 DOI: 10.1021/Ja2108307  0.364
2010 Spangenberg T, Aubry S, Kishi Y. Synthesis and structure assignment of the minor metabolite arising from the frog pathogen Mycobacterium liflandii. Tetrahedron Letters. 51: 1782-1785. PMID 20305830 DOI: 10.1016/J.Tetlet.2010.01.105  0.307
2010 Jackson KL, Li W, Chen CL, Kishi Y. Scalable and efficient synthesis of the mycolactone core. Tetrahedron. 66: 2263-2272. PMID 20228884 DOI: 10.1016/J.Tet.2010.02.010  0.326
2009 Liu S, Kim JT, Dong CG, Kishi Y. Catalytic enantioselective Cr-mediated propargylation: application to halichondrin synthesis. Organic Letters. 11: 4520-3. PMID 19810761 DOI: 10.1021/Ol9016595  0.342
2009 Dong CG, Henderson JA, Kaburagi Y, Sasaki T, Kim DS, Kim JT, Urabe D, Guo H, Kishi Y. New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks: reductive cyclization and oxy-Michael cyclization approaches. Journal of the American Chemical Society. 131: 15642-6. PMID 19807077 DOI: 10.1021/Ja9058487  0.378
2009 Kim DS, Dong CG, Kim JT, Guo H, Huang J, Tiseni PS, Kishi Y. New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks: double-inversion approach. Journal of the American Chemical Society. 131: 15636-41. PMID 19807076 DOI: 10.1021/Ja9058475  0.364
2009 Guo H, Dong CG, Kim DS, Urabe D, Wang J, Kim JT, Liu X, Sasaki T, Kishi Y. Toolbox approach to the search for effective ligands for catalytic asymmetric Cr-mediated coupling reactions. Journal of the American Chemical Society. 131: 15387-93. PMID 19795862 DOI: 10.1021/Ja905843E  0.318
2009 Yang YR, Kim DS, Kishi Y. Second generation synthesis of C27-C35 building block of E7389, a synthetic halichondrin analogue. Organic Letters. 11: 4516-9. PMID 19754145 DOI: 10.1021/Ol9016589  0.39
2009 Chen CL, Namba K, Kishi Y. Attempts to improve the overall stereoselectivity of the Ireland-Claisen rearrangement. Organic Letters. 11: 409-12. PMID 19128191 DOI: 10.1021/Ol8027225  0.323
2008 Wang Y, Cheon HS, Kishi Y. Unique reactivity of the Mukaiyama glycosidation catalyst (SnCl3ClO4) toward beta-mannopyranosides. Chemistry, An Asian Journal. 3: 319-26. PMID 18183569 DOI: 10.1002/Asia.200700297  0.663
2007 Kaburagi Y, Kishi Y. Effective Procedure for Selective Ammonolysis of Monosubstituted Oxiranes: Application to E7389 Synthesis. Tetrahedron Letters. 48: 8967-8971. PMID 19050739 DOI: 10.1016/J.Tetlet.2007.10.116  0.332
2007 Papaioannou N, Cheon HS, Lian Y, Kishi Y. Product-regulation mechanisms for fatty acid biosynthesis catalyzed by Mycobacterium smegmatis FAS I. Chembiochem : a European Journal of Chemical Biology. 8: 1775-80. PMID 17893901 DOI: 10.1002/Cbic.200700380  0.725
2007 Cheon HS, Lian Y, Kishi Y. Practical and scalable synthesis of alpha-(1-->4)-linked polysaccharides composed of 6-O-methyl-D-glucose. Organic Letters. 9: 3327-9. PMID 17658840 DOI: 10.1021/Ol071334X  0.697
2007 Cheon HS, Lian Y, Kishi Y. Highly stereoselective and iterative synthesis of alpha-(1-->4)-linked polysaccharides composed of 3-O-methyl-D-mannose. Organic Letters. 9: 3323-6. PMID 17658839 DOI: 10.1021/Ol0713335  0.712
2007 Hsu MC, Lee J, Kishi Y. Synthetic 3-O-methylmannose-containing polysaccharides (sMMPs): design and synthesis. The Journal of Organic Chemistry. 72: 1931-40. PMID 17274657 DOI: 10.1021/Jo061991N  0.304
2007 Meppen M, Wang Y, Cheon HS, Kishi Y. Synthetic 6-O-methylglucose-containing polysaccharides (sMGPs): design and synthesis. The Journal of Organic Chemistry. 72: 1941-50. PMID 17274656 DOI: 10.1021/Jo061990V  0.69
2007 Ma J, Cheon HS, Kishi Y. Chiral aggregates formed from methylated tetraenoic fatty acids: formation of both antipodes of chiral aggregates from a single enantiomer and time-dependent stereomutation. Organic Letters. 9: 319-22. PMID 17217294 DOI: 10.1021/Ol062834D  0.704
2007 Cheon HS, Wang Y, Ma J, Kishi Y. Complexation of fatty acids and fatty acid-CoAs with synthetic O-methylated polysaccharides. Chembiochem : a European Journal of Chemical Biology. 8: 353-9. PMID 17216665 DOI: 10.1002/Cbic.200600499  0.675
2007 Wang Y, Ma J, Cheon HS, Kishi Y. Aggregation behavior of tetraenoic fatty acids in aqueous solution. Angewandte Chemie (International Ed. in English). 46: 1333-6. PMID 17211902 DOI: 10.1002/Anie.200603979  0.656
2006 Seike H, Ghosh I, Kishi Y. Stereochemistry of sagittamide A: prediction and confirmation. Organic Letters. 8: 3865-8. PMID 16898837 DOI: 10.1021/Ol061582D  0.341
2006 Matsuura F, Hao J, Reents R, Kishi Y. Total synthesis and stereochemistry of pinnatoxins B and C. Organic Letters. 8: 3327-30. PMID 16836397 DOI: 10.1021/Ol0611548  0.338
2006 Hao J, Matsuura F, Kishi Y, Kita M, Uemura D, Asai N, Iwashita T. Stereochemistry of pteriatoxins A, B, and C. Journal of the American Chemical Society. 128: 7742-3. PMID 16771480 DOI: 10.1021/Ja061893J  0.568
2006 Matsuura F, Peters R, Anada M, Harried SS, Hao J, Kishi Y. Unified total synthesis of pteriatoxins and their diastereomers. Journal of the American Chemical Society. 128: 7463-5. PMID 16756299 DOI: 10.1021/Ja0618954  0.702
2005 Johannes JW, Wenglowsky S, Kishi Y. Biomimetic macrocycle-forming Diels-Alder reaction of an iminium dienophile: synthetic studies directed toward gymnodimine. Organic Letters. 7: 3997-4000. PMID 16119951 DOI: 10.1021/Ol051553N  0.679
2004 Judd TC, Bischoff A, Kishi Y, Adusumilli S, Small PL. Structure determination of mycolactone C via total synthesis. Organic Letters. 6: 4901-4. PMID 15606095 DOI: 10.1021/Ol0479996  0.762
2004 Adams CM, Ghosh I, Kishi Y. Validation of lanthanide chiral shift reagents for determination of absolute configuration: total synthesis of glisoprenin A. Organic Letters. 6: 4723-6. PMID 15575670 DOI: 10.1021/Ol048059O  0.337
2004 Ghosh I, Kishi Y, Tomoda H, Omura S. Use of a chiral praseodymium shift reagent in predicting the complete stereostructure of glisoprenin A. Organic Letters. 6: 4719-22. PMID 15575669 DOI: 10.1021/Ol048060N  0.305
2004 Kurosu M, Lin MH, Kishi Y. Fe/Cr- and Co/Cr-mediated catalytic asymmetric 2-haloallylations of aldehydes. Journal of the American Chemical Society. 126: 12248-9. PMID 15453741 DOI: 10.1021/Ja045557J  0.497
2004 Namba K, Jun HS, Kishi Y. A simple but remarkably effective device for forming the C8-C14 polycyclic ring system of halichondrin B. Journal of the American Chemical Society. 126: 7770-1. PMID 15212512 DOI: 10.1021/Ja047826B  0.309
2003 Higashibayashi S, Czechtizky W, Kobayashi Y, Kishi Y. Universal NMR databases for contiguous polyols. Journal of the American Chemical Society. 125: 14379-93. PMID 14624586 DOI: 10.1021/Ja0375481  0.576
2003 Kobayashi Y, Czechtizky W, Kishi Y. Complete stereochemistry of tetrafibricin. Organic Letters. 5: 93-6. PMID 12509899 DOI: 10.1021/Ol0272895  0.597
2003 Choi H, Demeke D, Kang F, Kishi Y, Nakajima K, Nowak P, Wan Z, Xie C. Synthetic studies on the marine natural product halichondrins Pure and Applied Chemistry. 75: 1-17. DOI: 10.1351/Pac200375010001  0.361
2003 Kobayashi Y, Hayashi N, Kishi Y. Application of chiral bidentate NMR solvents for assignment of the absolute configuration of alcohols: Scope and limitation Tetrahedron Letters. 44: 7489-7491. DOI: 10.1016/J.Tetlet.2003.08.022  0.62
2002 Xie C, Nowak P, Kishi Y. Synthesis of the C20-C26 building block of halichondrins via a regiospecific and stereoselective S(N)2' reaction. Organic Letters. 4: 4427-9. PMID 12465904 DOI: 10.1021/Ol026982P  0.314
2002 Kobayashi Y, Hayashi N, Kishi Y. Toward the creation of NMR databases in chiral solvents: bidentate chiral NMR solvents for assignment of the absolute configuration of acyclic secondary alcohols. Organic Letters. 4: 411-4. PMID 11820892 DOI: 10.1021/Ol0171160  0.618
2002 Kishi Y. Palytoxin: an inexhaustible source of inspiration—personal perspective Tetrahedron. 58: 6239-6258. DOI: 10.1016/S0040-4020(02)00624-5  0.328
2002 Schmid G, Fukuyama T, Akasaka K, Kishi Y. Synthetic Studies On Polyether Antibiotics. 4. Total Synthesis Of Monensin. 1. Stereocontrolled Synthesis Of The Left Half Of Monensin Cheminform. 10. DOI: 10.1002/Chin.197915380  0.311
2001 Li HY, Qiu YL, Moyroud E, Kishi Y. Synthesis of DNA Oligomers Possessing a Covalently Cross-Linked Watson-Crick Base Pair Model. Angewandte Chemie (International Ed. in English). 40: 1471-1475. PMID 29712372 DOI: 10.1002/1521-3773(20010417)40:8<1471::Aid-Anie1471>3.0.Co;2-I  0.417
2001 Topalov G, Kishi Y. Chlorophyll Catabolism Leading to the Skeleton of Dinoflagellate and Krill Luciferins: Hypothesis and Model Studies. Angewandte Chemie (International Ed. in English). 40: 3892-3894. PMID 29712155 DOI: 10.1002/1521-3773(20011015)40:20<3892::Aid-Anie3892>3.0.Co;2-H  0.78
2001 Topalov G, Kishi Y. Chlorophyll Catabolism Leading to the Skeleton of Dinoflagellate and Krill Luciferins: Hypothesis and Model Studies Financial support from the National Institutes of Health (NS 12108) is gratefully acknowledged. Angewandte Chemie (International Ed. in English). 40: 3892-3894. PMID 11668566 DOI: 10.1002/1521-3773(20011015)40:20<3892::AID-ANIE3892>3.0.CO;2-H  0.739
2001 Kobayashi Y, Tan CH, Kishi Y. Toward creation of a universal NMR database for stereochemical assignment: complete structure of the desertomycin/oasomycin class of natural products. Journal of the American Chemical Society. 123: 2076-8. PMID 11456839 DOI: 10.1021/Ja004154Q  0.693
2001 Kobayashi Y, Hayashi N, Kishi Y. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: NMR desymmetrization of meso compounds. Organic Letters. 3: 2253-5. PMID 11440592 DOI: 10.1021/Ol010110Q  0.644
2001 Hayashi N, Kobayashi Y, Kishi Y. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: scope and limitation. Organic Letters. 3: 2249-52. PMID 11440591 DOI: 10.1021/Ol010109R  0.662
2001 Kobayashi Y, Hayashi N, Tan CH, Kishi Y. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: proof of concept. Organic Letters. 3: 2245-8. PMID 11440590 DOI: 10.1021/Ol010108Z  0.719
2001 Li HY, Qiu YL, Moyroud E, Kishi Y. Synthesis of DNA Oligomers Possessing a Covalently Cross-Linked Watson-Crick Base Pair Model Financial support from the National Institutes of Health (Grant: NS 12108) is gratefully acknowledged. Angewandte Chemie (International Ed. in English). 40: 1471-1475. PMID 11317306 DOI: 10.1002/1521-3773(20010417)40:8<1471::AID-ANIE1471>3.0.CO;2-I  0.324
2000 Kobayashi Y, Tan CH, Kishi Y. Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Prediction. Angewandte Chemie (International Ed. in English). 39: 4279-4281. PMID 29711895 DOI: 10.1002/1521-3773(20001201)39:23<4279::Aid-Anie4279>3.0.Co;2-R  0.637
2000 Tan CH, Kobayashi Y, Kishi Y. Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Proof. Angewandte Chemie (International Ed. in English). 39: 4282-4284. PMID 29711890 DOI: 10.1002/1521-3773(20001201)39:23<4282::AID-ANIE4282>3.0.CO;2-U  0.628
2000 Numano F, Kishi Y, Tanaka A, Ohkawara M, Kakuta T, Kobayashi Y. Inflammation and atherosclerosis. Atherosclerotic lesions in Takayasu arteritis. Annals of the New York Academy of Sciences. 902: 65-76. PMID 10865826  0.546
2000 Qiu YL, Li HY, Topalov G, Kishi Y. Covalently cross-linked Watson-Crick base pair models. Part 2 Tetrahedron Letters. 41: 9425-9429. DOI: 10.1016/S0040-4039(00)01572-0  0.756
2000 Kobayashi Y, Tan CH, Kishi Y. Toward creation of a universal NMR database for stereochemical assignment: The case of 1,3,5-trisubstituted acyclic systems Helvetica Chimica Acta. 83: 2562-2571. DOI: 10.1002/1522-2675(20000906)83:9<2562::Aid-Hlca2562>3.0.Co;2-Z  0.703
1999 Lee J, Kobayashi Y, Tezuka K, Kishi Y. Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: proof of concept. Organic Letters. 1: 2181-4. PMID 10836073 DOI: 10.1021/Ol990379Y  0.664
1999 Kobayashi Y, Lee J, Tezuka K, Kishi Y. Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: the case of two contiguous propionate units. Organic Letters. 1: 2177-80. PMID 10836072 DOI: 10.1021/Ol9903786  0.643
1998 Kurosu M, Kishi Y. A Novel Example for Optical Resolution of Racemic Ketones Originating from Batrachotoxin Synthesis. The Journal of Organic Chemistry. 63: 6100-6101. PMID 11672234 DOI: 10.1021/Jo981416M  0.502
1998 Moncada G, Kobayashi Y, Kaneko E, Nishiwaki Y, Kishi Y, Numano F. Subclavian steal syndrome secondary to Takayasu arteritis. International Journal of Cardiology. 66: S231-6. PMID 9951824  0.546
1998 Moncada G, Kobayashi Y, Maruyama Y, Kato T, Noda M, Kakuta T, Kishi Y, Numano F. Long-term patency of an aorta-aortic graft bypass in a patient with Takayasu arteritis. Internal Medicine (Tokyo, Japan). 37: 934-9. PMID 9868955  0.536
1998 Ravishankar R, Surolia A, Vijayan M, Lim S, Kishi Y. Preferred Conformation ofC-Lactose at the Free and Peanut Lectin Bound States Journal of the American Chemical Society. 120: 11297-11303. DOI: 10.1021/Ja982193K  0.316
1998 Hayward MM, Roth RM, Duffy KJ, Dalko PI, Stevens KL, Guo J, Kishi Y. Totalsynthese Von Altohyrtin A (Spongistatin 1) : Teil 2 Angewandte Chemie. 110: 202-206. DOI: 10.1002/(Sici)1521-3757(19980116)110:1/2<202::Aid-Ange202>3.0.Co;2-J  0.514
1998 Guo J, Duffy KJ, Stevens KL, Dalko PI, Roth RM, Hayward MM, Kishi Y. Totalsynthese von Altohyrtin A (Spongistatin 1): Teil 1 Angewandte Chemie. 110: 198-202. DOI: 10.1002/(Sici)1521-3757(19980116)110:1/2<198::Aid-Ange198>3.0.Co;2-0  0.514
1997 Stamos DP, Chen aSS, Kishi Y. New Synthetic Route to the C.14−C.38 Segment of Halichondrins Journal of Organic Chemistry. 62: 7552-7553. DOI: 10.1021/Jo971713B  0.315
1997 Shi Y, Peng aLF, Kishi Y. Enantioselective Total Synthesis of Fumonisin B2 Journal of Organic Chemistry. 62: 5666-5667. DOI: 10.1021/Jo9711347  0.309
1996 Numano F, Kobayashi Y, Maruyama Y, Kakuta T, Miyata T, Kishi Y. Takayasu arteritis: clinical characteristics and the role of genetic factors in its pathogenesis. Vascular Medicine (London, England). 1: 227-33. PMID 9546941  0.531
1996 Zheng W, DeMattei JA, Wu JP, Duan JJW, Cook LR, Oinuma H, Kishi Y. Complete relative stereochemistry of maitotoxin Journal of the American Chemical Society. 118: 7946-7968. DOI: 10.1021/Ja961230+  0.395
1995 Strichartz GR, Hall S, Magnani B, Hong CY, Kishi Y, Debin JA. The potencies of synthetic analogues of saxitoxin and the absolute stereoselectivity of decarbamoyl saxitoxin. Toxicon : Official Journal of the International Society On Toxinology. 33: 723-37. PMID 7676464 DOI: 10.1016/0041-0101(95)00031-G  0.339
1995 Wei A, Haudrechy A, Audin C, Jun H, Haudrechy-Bretel N, Kishi Y. Preferred Conformations of C-Glycosides. 14. Synthesis and Conformational Analysis of Carbon Analogs of the Blood Group Determinant H-Type II Journal of Organic Chemistry. 60: 2160-2169. DOI: 10.1021/Jo00112A040  0.517
1995 Wei A, Boy KM, Kishi Y. Biological Evaluation of Rationally Modified Analogs of the H-Type II Blood Group Trisaccharide. A Correlation between Solution Conformation and Binding Affinity Journal of the American Chemical Society. 117: 9432-9436. DOI: 10.1021/Ja00142A008  0.453
1994 Tse B, Kishi Y. Conformationally Rigid Tricyclic Tripods: Synthesis and Application to Preparation of Enterobactin Analogs Journal of Organic Chemistry. 59: 7807-7814. DOI: 10.1021/Jo00104A043  0.326
1994 O'Leary DJ, Kishi Y. Preferred Conformation of C-Glycosides. 13. A Comparison of the Conformational Behavior of Several C-, N-, and O-Furanosides Journal of Organic Chemistry. 59: 6629-6636. DOI: 10.1021/Jo00101A022  0.303
1994 Wei A, Kishi Y. Preferred conformation of C-glycosides. 12. Synthesis and conformational analysis of .alpha.,.alpha.-, .alpha.,.beta.-, and .beta.,.beta.-C-trehaloses Journal of Organic Chemistry. 59: 88-96. DOI: 10.1021/Jo00080A016  0.507
1994 Grinsteiner TJ, Kishi Y. Synthetic studies towards batrachotoxin 1. A furan-based intramolecular diels-alder route to construct the a-d ring system Tetrahedron Letters. 35: 8333-8336. DOI: 10.1016/S0040-4039(00)74400-5  0.326
1993 Shimomura O, Musicki B, Kishi Y, Inouye S. Light-emitting properties of recombinant semi-synthetic aequorins and recombinant fluorescein-conjugated aequorin for measuring cellular calcium. Cell Calcium. 14: 373-8. PMID 8519061 DOI: 10.1016/0143-4160(93)90041-4  0.434
1993 Shimomura O, Satoh S, Kishi Y. Structure and non-enzymatic light emission of two luciferin precursors isolated from the luminous mushroom Panellus stipticus. Journal of Bioluminescence and Chemiluminescence. 8: 201-5. PMID 8372704 DOI: 10.1002/Bio.1170080403  0.462
1993 Shimomura O, Kishi Y, Inouye S. The relative rate of aequorin regeneration from apoaequorin and coelenterazine analogues. The Biochemical Journal. 296: 549-51. PMID 8280050 DOI: 10.1042/Bj2960549  0.455
1993 O'Leary DJ, Kishi Y. Preferred conformation of C-glycosides. 11. C-Sucrose: new practical synthesis, structural reassignment, and solid-state and solution conformation of its octaacetate Journal of Organic Chemistry. 58: 304-306. DOI: 10.1021/Jo00054A006  0.36
1993 Duan JJ-, Kishi Y. Synthetic studies on halichondrins: A new practical synthesis of the C.1–C.12 segment Tetrahedron Letters. 34: 7541-7544. DOI: 10.1016/S0040-4039(00)60394-5  0.37
1992 Haneda T, Goekjian PG, Kim SH, Kishi Y. Preferred conformation of C-glycosides. 10. Synthesis and conformational analysis of carbon trisaccharides Journal of Organic Chemistry. 57: 490-498. DOI: 10.1021/Jo00028A019  0.33
1992 Wang Y, Babirad SA, Kishi Y. Preferred conformation of C-glycosides. 8. Synthesis of 1,4-linked carbon disaccharides Journal of Organic Chemistry. 57: 468-481. DOI: 10.1021/Jo00028A017  0.345
1992 Fang FG, Kishi Y, Matclich MC, Scola PM. Synthetic studies towards halichondrins synthesis of the left halves of norhalichondrins and homohalichondrins Tetrahedron Letters. 33: 1557-1560. DOI: 10.1016/S0040-4039(00)91673-3  0.3
1992 Buszek KR, Fang FG, Forsyth CJ, Jung SH, Kishi Y, Scola PM, Yoon SK. Synthetic Studies Towards Halichondrins: Synthesis of the Left Half of Halichondrins Tetrahedron Letters. 33: 1553-1556. DOI: 10.1016/S0040-4039(00)91672-1  0.544
1992 Aicher TD, Buszek KR, Fang FG, Forsyth CJ, Jung SH, Kishi Y, Scola PM. Synthetic Studies towards Halichondrins: Synthesis of the C.27-C.38 Segment Tetrahedron Letters. 33: 1549-1552. DOI: 10.1016/S0040-4039(00)91671-X  0.58
1990 Shimomura O, Inouye S, Musicki B, Kishi Y. Recombinant aequorin and recombinant semi-synthetic aequorins. Cellular Ca2+ ion indicators. The Biochemical Journal. 270: 309-12. PMID 2400391 DOI: 10.1042/Bj2700309  0.451
1990 Kong F, Kishi Y, Perez-Sala D, Rando RR. The stereochemical requirement for protein kinase C activation by 3-methyldiglycerides matches that found in naturally occurring tumor promoters aplysiatoxins. Febs Letters. 274: 203-6. PMID 2253773 DOI: 10.1016/0014-5793(90)81364-T  0.329
1990 Campbell AK, Sala-Newby G, Aston PJ, Kalsheker N, Kishi Y, Shimomura O. From Luc and Phot genes to the hospital bed. Journal of Bioluminescence and Chemiluminescence. 5: 131-9. PMID 1970919 DOI: 10.1002/Bio.1170050209  0.429
1989 Shimomura O, Musicki B, Kishi Y. Semi-synthetic aequorins with improved sensitivity to Ca2+ ions. The Biochemical Journal. 261: 913-20. PMID 2803250 DOI: 10.1042/Bj2610913  0.442
1989 Kishi Y. Natural products synthesis: palytoxin Pure and Applied Chemistry. 61: 313-324. DOI: 10.1351/Pac198961030313  0.388
1989 Nakamura H, Kishi Y, Shimomura O, Morse D, Hastings JW. Structure of dinoflagellate luciferin and its enzymic and nonenzymic air-oxidation products Journal of the American Chemical Society. 111: 7607-7611. DOI: 10.1021/Ja00201A050  0.436
1989 Rowley M, Tsukamoto M, Kishi Y. Total synthesis of (+)-ophiobolin C Journal of the American Chemical Society. 111: 2735-2737. DOI: 10.1021/Ja00189A069  0.393
1988 Shimomura O, Musicki B, Kishi Y. Semi-synthetic aequorin. An improved tool for the measurement of calcium ion concentration. The Biochemical Journal. 251: 405-10. PMID 3401214 DOI: 10.1042/Bj2510405  0.446
1988 Miller WH, Ryckman DM, Goekjian PG, Wang Y, Kishi Y. Preferred conformation of C-glycosides. 5. Experimental support for the conformational similarity between C- and O-disaccharides Journal of Organic Chemistry. 53: 5580-5582. DOI: 10.1021/Jo00258A046  0.313
1988 Nakamura H, Musicki B, Kishi Y, Shimomura O. Structure of the light emitter in krill (Euphausia pacifica) bioluminescence Journal of the American Chemical Society. 110: 2683-2685. DOI: 10.1021/Ja00216A070  0.433
1988 Nakamura H, Kishi Y, Shimomura O. Panal: A possible precursor of fungal luciferin Tetrahedron. 44: 1597-1602. DOI: 10.1016/S0040-4020(01)86719-3  0.478
1987 Babirad SA, Wang Y, Kishi Y. Synthesis of C-disaccharides Journal of Organic Chemistry. 52: 1370-1372. DOI: 10.1021/Jo00383A045  0.393
1987 Goekjian PG, Wu TC, Kishi Y. Preferred conformation of C-glycosides. 6. Conformational similarity of glycosides and corresponding C-glycosides Journal of Organic Chemistry. 52: 4819-4823. DOI: 10.1021/Jo00022A038  0.328
1987 Uenishi J, Beau JM, Armstrong RW, Kishi Y. Dramatic rate enhancement of Suzuki diene synthesis: its application to palytoxin synthesis Journal of the American Chemical Society. 109: 4756-4758. DOI: 10.1021/Ja00249A069  0.313
1986 Musicki B, Kishi Y, Shimomura O. Structure of the functional part of photoprotein aequorin Journal of the Chemical Society, Chemical Communications. 1566-1568. DOI: 10.1039/C39860001566  0.499
1985 Lee HW, Kishi Y. Synthesis of mono- and unsymmetrical bis-orthoesters of scyllo-inositol Journal of Organic Chemistry. 50: 4402-4404. DOI: 10.1021/Jo00222A046  0.351
1983 Ko SS, Klein LL, Pfaff KP, Kishi Y. Synthetic studies on palytoxin. Stereocontrolled, practical synthesis of the C.101-C.115 segment Tetrahedron Letters. 23: 4415-4418. DOI: 10.1016/S0040-4039(00)81682-2  0.372
1983 CHA JK, CHRIST WJ, FINAN JM, FUJIOKA H, KISHI Y, KLEIN LL, KO SS, LEDER J, MCWHORTER WWJ, PFAFF K, YONAGA M, UEMURA D, HIRATA Y. ChemInform Abstract: STEREOCHEMISTRY OF PALYTOXIN. PART 4. COMPLETE STRUCTURE Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198312364  0.573
1983 Klein LL, Mcwhorter WWJ, Ko SS, Pfaff K-, Kishi Y, Uemura D, Hirata Y. Stereochemistry Of Palytoxin. Part 1. C85-C115 Segment Cheminform. 14. DOI: 10.1002/Chin.198312361  0.599
1982 McNamara JM, Kishi Y. Practical asymmetric synthesis of aklavinone Journal of the American Chemical Society. 104: 7371-7372. DOI: 10.1021/Ja00389A102  0.303
1982 Fujioka H, Christ WJ, Cha JK, Leder J, Kishi Y, Uemura D, Hirata Y. Stereochemistry of palytoxin. Part 3. C7-C51 segment Journal of the American Chemical Society. 104: 7367-7369. DOI: 10.1021/Ja00389A100  0.599
1982 Ko SS, Finan JM, Yonaga M, Kishi Y, Uemura D, Hirata Y. Stereochemistry of palytoxin. Part 2. C1-C6, C47-C74, and C77-C83 segments Journal of the American Chemical Society. 104: 7364-7367. DOI: 10.1021/Ja00389A099  0.604
1982 Klein L, McWhorter WW, Ko SS, Pfaff KP, Kishi Y, Uemura D, Hirata Y. Stereochemistry of palytoxin. Part 1. C85-C115 segment Journal of the American Chemical Society. 104: 7362-7364. DOI: 10.1021/Ja00389A098  0.538
1981 Pearlman BA, McNamara JM, Hasan I, Hatakeyama S, Sekizaki H, Kishi Y. Practical total synthesis of (.+-.)-aklavinone and total synthesis of aklavin Journal of the American Chemical Society. 103: 4248-4251. DOI: 10.1021/Ja00404A047  0.327
1981 Iio H, Nagaoka H, Kishi Y. A model study for the biomimetic-type synthesis of rifamycin S Tetrahedron Letters. 22: 2451-2454. DOI: 10.1016/S0040-4039(01)92930-2  0.334
1981 Pearlman BA, Mcnamara JM, Hasan I, Hatakeyama S, Sekizaki H, Kishi Y. Practical total synthesis of (.+-.)-aklavinone and total synthesis of aklavin Cheminform. 12. DOI: 10.1002/Chin.198143317  0.327
1980 Iio H, Nagaoka H, Kishi Y. Total synthesis of rifamycins. 2. Total synthesis of racemic rifamycin S Journal of the American Chemical Society. 102: 7965-7967. DOI: 10.1021/Ja00547A038  0.332
1980 Nagaoka H, Rutsch W, Schmid G, Iio H, Johnson MR, Kishi Y. Total synthesis of rifamycins. 1. Stereocontrolled synthesis of the aliphatic building block Journal of the American Chemical Society. 102: 7962-7965. DOI: 10.1021/Ja00547A037  0.335
1980 Fujimoto R, Kishi Y, Blount JF. Total synthesis of (.+-.)-gephyrotoxin Journal of the American Chemical Society. 102: 7154-7156. DOI: 10.1021/Ja00543A067  0.34
1979 Hutchison AJ, Kishi Y. Stereospecific total synthesis of dl-austamide Journal of the American Chemical Society. 101: 6786-6788. DOI: 10.1021/Ja00516A067  0.332
1979 Fukuyama T, Akasaka K, Karanewsky DS, Wang CLJ, Schmid G, Kishi Y. Synthetic studies on polyether antibiotics. 6. Total synthesis of monensin. 3. Stereocontrolled total synthesis of monensin Journal of the American Chemical Society. 101: 262-263. DOI: 10.1021/Ja00495A066  0.601
1979 Schmid G, Fukuyama T, Akasaka K, Kishi Y. Synthetic studies on polyether antibiotics. 4. Total synthesis of monensin. 1. Stereocontrolled synthesis of the left half of monensin Journal of the American Chemical Society. 101: 259-260. DOI: 10.1021/Ja00495A064  0.597
1979 Johnson MR, Nakata T, Kishi Y. Stereo- and regioselective methods for the synthesis of three consecutive asymmetric units found in many natural products Tetrahedron Letters. 20: 4343-4346. DOI: 10.1016/S0040-4039(01)86584-9  0.369
1979 FUKUYAMA T, AKASAKA K, KARANEWSKY DS, WANG CJ, SCHMID G, KISHI Y. ChemInform Abstract: SYNTHETIC STUDIES ON POLYETHER ANTIBIOTICS. 6. TOTAL SYNTHESIS OF MONENSIN. 3. STEREOCONTROLLED TOTAL SYNTHESIS OF MONENSIN Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197915382  0.603
1978 Nakata T, Schmid G, Vranesic B, Okigawa M, Smith-Palmer T, Kishi Y. A total synthesis of lasalocid A Journal of the American Chemical Society. 100: 2933-2935. DOI: 10.1021/Ja00477A081  0.34
1978 Nakata T, Kishi Y. Synthetic studies on polyether antibiotics. III. A stereocontrolled synthesis of isolasalocid ketone from acyclic precursors Tetrahedron Letters. 19: 2745-2748. DOI: 10.1016/S0040-4039(01)94850-6  0.343
1978 Fukuyama T, Vranesic B, Negri D, Kishi Y. Synthetic studies on polyether antibiotics. II. Stereocontrolled syntheses of epoxides of bishomoallylic alcohols. Tetrahedron Letters. 19: 2741-2744. DOI: 10.1016/S0040-4039(01)94849-X  0.546
1978 Hutchison AJ, Kishi Y. The stereospecific synthesis of tetrahydroaustamide Tetrahedron Letters. 19: 539-542. DOI: 10.1016/S0040-4039(01)85326-0  0.344
1977 Nakatsubo F, Cocuzza AJ, Keeley DE, Kishi Y. Synthetic studies toward mitomycins. 1. Total synthesis of deiminomitomycin A. Journal of the American Chemical Society. 99: 4835-4836. PMID 874235 DOI: 10.1021/Ja00456A056  0.352
1977 Nakatsubo F, Fukuyama T, Cocuzza AJ, Kishi Y. Synthetic studies toward mitomycins. 2. Total synthesis of dl-porfiromycin Journal of the American Chemical Society. 99: 8115-8116. DOI: 10.1021/Ja00466A089  0.344
1977 Fukuyama T, Nakatsubo F, Cocuzza AJ, Kishi Y. Synthetiic studies toward mitomycins. III. Total syntheses of mitomycins A and C Tetrahedron Letters. 18: 4295-4298. DOI: 10.1016/S0040-4039(01)83489-4  0.355
1976 Fukuyama T, Kishi Y. A total synthesis of gliotoxin. Journal of the American Chemical Society. 98: 6723-4. PMID 61223  0.558
1976 Fukuyama T, Nakatsuka S, Kishi Y. A new synthesis of epidithiapiperazinediones Tetrahedron Letters. 17: 3393-3396. DOI: 10.1016/S0040-4039(00)93053-3  0.311
1975 Nakatsuka S, Tanino H, Kishi Y. Letter: Biogenetic-type synthesis of penicillin-cephalosporin antibiotics. I. A stereocontrolled synthesis of the penam- and cephem-ring systems from an acyclic tripeptide equivalent. Journal of the American Chemical Society. 97: 5008-5010. PMID 1165351 DOI: 10.1021/Ja00850A042  0.31
1975 Fukuyama T, Dunkerton LV, Aratani M, Kishi Y. Letter: Synthetic studies on histrionicotoxins. II. A practical synthetic route to (plus or minus)-perhydro-and (plus or minus)-octahydrohistrionicotoxin. The Journal of Organic Chemistry. 40: 2011-12. PMID 1133613 DOI: 10.1021/Jo00901A038  0.552
1975 Aratani M, Dunkerton LV, Fukuyama T, Kishi Y, Kakoi H, Sugiura S, Inoue S. Letter: Synthetic studies on histrionicotoxins. I. A stereocontrolled synthesis of (plus or minus)-perhydrohistrionicotoxin. The Journal of Organic Chemistry. 40: 2009-11. PMID 1133612 DOI: 10.1021/Jo00901A037  0.606
1975 Sasaki K, Fukuyama T, Nakatsuka S, Kishi Y. X-Ray structure determination of 3,6-p-anisylidenedithio-3-ethyl-NN′-dimethylpiperazine-2,5-dione Journal of the Chemical Society, Chemical Communications. 542-543. DOI: 10.1039/C39750000542  0.553
1975 Nakatsuka S, Tanino H, Kishi Y. Biogenetic-Type Synthesis Of Penicillin-Cephalosporin Antibiotics Part 1, A Stereocontrolled Synthesis Of The Penam- And Cephem-Ring Systems From An Acyclic Tripeptide Equivalent Cheminform. 6. DOI: 10.1002/Chin.197544402  0.31
1973 Kishi Y, Nakatsuka S, Fukuyama T, Havel M. A total synthesis of sporidesmin A. Journal of the American Chemical Society. 95: 6493-5. PMID 4733402 DOI: 10.1002/Chin.197347320  0.558
1973 Kishi Y, Fukuyama T, Nakatsuka S. A total synthesis of dehydrogliotoxin. Journal of the American Chemical Society. 95: 6492-3. PMID 4733401 DOI: 10.1002/Chin.197347476  0.558
1973 Kobayashi Y, Komiya I, Utsuno Y, Kishi Y, Hayashi Y. [Symposium. Our methods in public health nursing]. [Hokenfu Zasshi] the Japanese Journal For Public Health Nurse. 29: 698-711. PMID 4491700  0.537
1973 Kobayashi Y, Komiya I, Utsuno Y, Kishi Y, Hayashi Y. [Symposium. Our methods in public health nursing activities]. [Hokenfu Zasshi] the Japanese Journal For Public Health Nurse. 29: 774-83. PMID 4491179  0.537
1973 Terashima T, Idaka E, Kishi Y, Goto T. Biosynthesis of nigrifactin Journal of the Chemical Society, Chemical Communications. 75-76. DOI: 10.1039/C39730000075  0.304
1973 Kishi Y, Fukuyama T, Nakatsuka S. New method for the synthesis of epidithiodiketopiperazines Journal of the American Chemical Society. 95: 6490-6492. DOI: 10.1021/Ja00800A077  0.57
1973 Kishi Y, Fukuyama T, Aratani M, Nakatsubo F, Goto T, Inoue S, Tanino H, Sugiura S, Kakoi H. Synthese-Untersuchungen An Tetrodotoxin Und Verwandten Verbindungen 4. Mitt. Stereospezifische Totalsynth. Von Dl-Tetrodotoxin Cheminform. 4. DOI: 10.1002/Chin.197310356  0.348
1972 Kishi Y, Fukuyama T, Aratani M, Nakatsubo F, Goto T. Synthetic studies on tetrodotoxin and related compounds. IV. Stereospecific total syntheses of DL-tetrodotoxin. Journal of the American Chemical Society. 94: 9219-21. PMID 4642371 DOI: 10.1021/Ja00781A039  0.549
1972 Kishi Y, Aratani M, Fukuyama T, Nakatsubo F, Goto T. Synthetic studies on tetrodotoxin and related compounds. 3. A stereospecific synthesis of an equivalent of acetylated tetrodamine. Journal of the American Chemical Society. 94: 9217-9. PMID 4642370 DOI: 10.1021/Ja00781A038  0.571
1972 Kishi Y, Aratani M, Tanino H, Fukuyama T, Goto T, Inoue S, Sugiura S, Kakoi H. New epoxidation with m-chloroperbenzoic acid at elevated temperatures Journal of the Chemical Society, Chemical Communications. 64-65. DOI: 10.1039/C39720000064  0.324
1972 Kishi Y, Tanino H, Goto T. The structure confirmation of the light-emitting moiety of bioluminescent jellyfish Tetrahedron Letters. 13: 2747-2748. DOI: 10.1016/S0040-4039(01)84922-4  0.312
1972 Kishi Y, Aratani M, Tanino H, Fukuyama T, Goto T, Inoue S, Sugiura S, Kakoi H. Eine Neue Epoxidierung Mit M-Chlorperbenzoesaeure Bei Erhoehter Temperatur Cheminform. 3. DOI: 10.1002/Chin.197217254  0.32
1972 Kishi Y, Nakatsuka S, Fukuyama T, Goto T. Eine Stereoselektive Decarboxylierung Von 1,6-Dimethyl-3-(3′-Indolyl)-Methyl-3-Carboxy-2,5-Piperazin-Dion Cheminform. 3. DOI: 10.1002/Chin.197210313  0.323
1970 Kishi Y, Nakatsubo F, Aratani M, Goto T, Inoue S. Synthetic approach towards tetrodotoxin. I. Diels-Alder reaction of alpha-oximinoethylbenzooquinones with butadiene. Tetrahedron Letters. 5127-8. PMID 5501331 DOI: 10.1016/S0040-4039(00)96956-9  0.315
1970 Nakatsubo F, Kishi Y, Goto T. Synthesis and stereochemistry of latia luciferin Tetrahedron Letters. 11: 381-382. DOI: 10.1016/0040-4039(70)80090-9  0.419
1968 Kishi Y, Matsuura S, Inoue S, Shimomura O, Goto T. Luciferin and luciopterin isolated from the Japanese firefly, Luciola cruciata. Tetrahedron Letters. 2847-50. PMID 5655703 DOI: 10.1016/S0040-4039(00)75644-9  0.396
1965 Goto T, Kishi Y, Takahashi S, Hirata Y. Tetrodotoxin. Tetrahedron. 21: 2059-88. PMID 5896483  0.308
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