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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