Year |
Citation |
Score |
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 |
0.499 |
|
2009 |
Takita M, Tanaka Y, Matsumura T, Kishi Y, Kodama Y, Nishimura T, Goto T, Nagai M, Kami M. Regional social system for specialized medical care in hematologic malignancies: a pilot study. Rural and Remote Health. 9: 1106. PMID 19637934 |
0.318 |
|
1991 |
Ohki K, Kishi Y, Nishino Y, Sumiya M, Kimura T, Goto T, Nakai M, Ikuta K. Noninfectious doughnut-shaped human immunodeficiency virus type 1 can induce syncytia mediated by fusion of the particles with CD4-positive cells. Journal of Acquired Immune Deficiency Syndromes. 4: 1233-40. PMID 1682474 |
0.314 |
|
1977 |
Sakabe N, Goto T, Hirata Y. Structure of citreoviridin, a mycotoxin produced by penicillium citreo-viride molded on rice Tetrahedron. 33: 3077-3081. DOI: 10.1016/0040-4020(77)80452-3 |
0.415 |
|
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 |
0.415 |
|
1973 |
Kishi Y, Aratani M, Fukuyama T, Nakatsubo F, Goto T, Inoue S, Tanino H, Sugiura S, Kakoi H. Synth.-Untersuchungen An Tetrodotoxin Und Verwandten Verbindungen 3. Mitt. Stereospezifische Synth. Einer ′Aequivalenten′ Verbindung Von Acetyliertem Tetrodamin Cheminform. 4. DOI: 10.1002/Chin.197311338 |
0.408 |
|
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 |
0.46 |
|
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 |
0.573 |
|
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 |
0.576 |
|
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 |
0.434 |
|
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 |
0.451 |
|
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 |
0.441 |
|
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 |
0.433 |
|
1971 |
Kishi Y, Nakatsuka S, Fukuyama T, Goto T. A stereoselective decarboxylation of 1,6-dimethyl-3-(3′-indolyl)methyl-3-carboxy-2,5-piperazinedione Tetrahedron Letters. 12: 4657-4660. DOI: 10.1016/S0040-4039(01)97555-0 |
0.426 |
|
1971 |
Kishi Y, Nakatsubo F, Aratani M, Goto T, Inoue S, Kakoi H, Sugiura S. Synthesewege Zum Tetrodotoxin 1. Mitt. Diels-Alder-Rk. Von Alpha-Oximinoaethyl-Benzochinonen Mit Butadien 2. Mitt. Eine Stereospezifische Synth. Einer Verbindung Mit Den Gleichen Sechs Chiralen Zentren Im Cyclohexanring Wie Im Tetrodo Cheminform. 2. DOI: 10.1002/Chin.197113292 |
0.405 |
|
1970 |
Kishi Y, Nakatsubo F, Aratani M, Goto T, Inoue S. Synthetic approach towards tetrodotoxin. II. A stereospecific synthesis of a compound having the same six chiral centers on the cyclohexane ring as those of tetrodotoxin. Tetrahedron Letters. 5129-32. PMID 5501332 |
0.417 |
|
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 |
0.419 |
|
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 |
0.458 |
|
1969 |
Kishi Y, Sugiura S, Inoue S, Goto T. [Synthesis of Cypridina luciferin and related compounds. 3. Synthesis of cypridina luciferin]. Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan. 89: 1657-60. PMID 5392847 DOI: 10.1248/Yakushi1947.89.12_1657 |
0.483 |
|
1969 |
Sugiura S, Inoue S, Kishi Y, Goto T. [Synthesis of Cypridina luciferin and related compounds. II. Synthesis of etioluciferamine]. Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan. 89: 1652-6. PMID 5392846 DOI: 10.1248/Yakushi1947.89.12_1652 |
0.491 |
|
1969 |
Sugiura S, Inoue S, Kishi Y, Goto T. [Synthesis of Cypridina luciferin and related compounds. I. Synthesis of 2-amino-5-(3-indolyl)-pyrazine]. Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan. 89: 1646-51. PMID 5392845 DOI: 10.1248/Yakushi1947.89.12_1646 |
0.486 |
|
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 |
0.416 |
|
1968 |
Goto T, Kishi Y. Luciferins, bioluminescent substances. Angewandte Chemie (International Ed. in English). 7: 407-14. PMID 4385699 DOI: 10.1002/anie.196804071 |
0.31 |
|
1966 |
Wada H, Goto G, Goto T, Hirata Y. Two new triterpenes having a -diol function obtained from Tetrahedron Letters. 7: 3461-3464. DOI: 10.1016/S0040-4039(01)82811-2 |
0.36 |
|
1966 |
Kishi Y, Goto T, Eguchi S, Hirata Y, Watanabe E, Aoyama T. Cypridina bioluminescence II structural studies of luciferin by means of a high resolution mass spectrometer and an amino acid analyzer Tetrahedron Letters. 7: 3437-3444. DOI: 10.1016/S0040-4039(01)82807-0 |
0.403 |
|
1966 |
Kishi T, Goto T, Hirata Y, Shimomura O, Johnson FH. Cypridina bioluminescence I Sructure of luciferin Tetrahedron Letters. 7: 3427-3436. DOI: 10.1016/S0040-4039(01)82806-9 |
0.338 |
|
1965 |
Goto T, Kishi Y, Takahashi S, Hirata Y. Tetrodotoxin. Tetrahedron. 21: 2059-88. PMID 5896483 |
0.443 |
|
1965 |
Nakamura S, Yamada T, Wada H, Inoue Y, Goto T, Hirata Y. The structures of five new triterpenoids obtained from Tetrahedron Letters. 6: 2017-2022. DOI: 10.1016/S0040-4039(01)83902-2 |
0.423 |
|
1964 |
Takahashi S, Goto T, Hirata Y. IR-Spectra of Guanidinium Group in Tetrodotoxin Derivatives Nippon Kagaku Kaishi. 85. DOI: 10.1246/Nikkashi1948.85.9_586 |
0.359 |
|
1964 |
Takahashi S, Goto T, Hirata Y. Structures of Anhydrotetrodoic Acid and Bromoanhydrotetrodoic Lactone Nippon Kagaku Kaishi. 85. DOI: 10.1246/Nikkashi1948.85.9_579 |
0.421 |
|
1964 |
Kishi Y, Goto T, Hirata Y. Structure of Tetrodoic Add, a Hydrolysis Product of Tetrodotoxin Nippon Kagaku Kaishi. 85. DOI: 10.1246/Nikkashi1948.85.9_572 |
0.417 |
|
1964 |
Kishi Y, Taguchi H, Goto T, Hirata Y. Structure of C9-Base, C8-Base and Oxy-C8-Base, Alkaline and Acid Degradation Products of Tetrodotoxin and its Derivatives Nippon Kagaku Kaishi. 85. DOI: 10.1246/Nikkashi1948.85.9_564 |
0.363 |
|
1964 |
Goto T, Takahashi S, Kishi Y, Hirata Y. Extraction and Purification of Tetrodotoxin Nippon Kagaku Kaishi. 85. DOI: 10.1246/Nikkashi1948.85.8_508 |
0.328 |
|
1964 |
Goto T, Kishi Y, Takahashi S, Hirata Y. Acetylation of Tetrodotoxin Nippon Kagaku Kaishi. 85. DOI: 10.1246/Nikkashi1948.85.10_667 |
0.367 |
|
1964 |
Goto T, Kishi Y, Takahashi S, Hirata Y. The Structures of Tetrodotoxin and Anhydroepitetrodotoxin Nippon Kagaku Kaishi. 85. DOI: 10.1246/Nikkashi1948.85.10_661 |
0.41 |
|
1964 |
Goto T, Takahashi S, Kishi Y, Hirata Y. Tetrodotoxin. III. A Revised Molecular Formula for Tetrodotoxin Bulletin of the Chemical Society of Japan. 37: 283-284. DOI: 10.1246/Bcsj.37.283 |
0.358 |
|
1964 |
Sakabe N, Goto T, Hirata Y. The structure of citreoviridin, a toxic compound produced by . molded on rice Tetrahedron Letters. 5: 1825-1830. DOI: 10.1016/S0040-4039(01)89494-6 |
0.441 |
|
1964 |
Goto T, Kishi Y, Takahashi S, Hirata Y. Further studies on the structure of tetrodotoxin Tetrahedron Letters. 5: 779-786. DOI: 10.1016/0040-4039(64)83035-5 |
0.431 |
|
1963 |
Goto T, Kakisawa H, Hirata Y. The structure of grifolin, an antibiotic from a basidiomycete. Tetrahedron. 19: 2079-83. PMID 5879215 DOI: 10.1016/0040-4020(63)85023-1 |
0.429 |
|
1963 |
Goto T, Takahashi S, Kishi Y, Hirata Y, Tomiie Y, Nitta I. The structure and stereochemistry of tetrodotoxin Tetrahedron Letters. 4: 2115-2118. DOI: 10.1016/S0040-4039(01)90980-3 |
0.438 |
|
1962 |
Goto T, Kishi Y, Hirata Y. Structure of the C8-Base, an Acid Degradation Product of Tetrodotoxin Bulletin of the Chemical Society of Japan. 35: 1244-1245. DOI: 10.1246/Bcsj.35.1244 |
0.412 |
|
1962 |
Goto T, Kishi Y, Hirata Y. Structure of the C9-Base, an Alkaline Degradation Product of Tetrodotoxin Bulletin of the Chemical Society of Japan. 35: 1045-1046. DOI: 10.1246/Bcsj.35.1045 |
0.405 |
|
1962 |
Goto T, Kato N, Hirata Y, Hayashi Y. The Structure of Leonurine Tetrahedron Letters. 3: 545-548. DOI: 10.1016/S0040-4039(00)76926-7 |
0.425 |
|
1961 |
Goto T, Fieser LF. Mechanism Of The Serini Reaction Journal of the American Chemical Society. 83: 251-252. DOI: 10.1021/Ja01462A054 |
0.363 |
|
1960 |
Fieser LF, Yuan C, Goto T. Reaction of cholestenolone acetates with ethanedithiol Journal of the American Chemical Society. 82: 1996-2001. DOI: 10.1021/Ja01493A037 |
0.377 |
|
1960 |
Fieser LF, Bhattacharyya BK, Goto T. Reactions of ketone 104 Journal of the American Chemical Society. 82: 1706-1709. DOI: 10.1021/Ja01492A045 |
0.376 |
|
1960 |
Fieser LF, Goto T, Bhattacharyya BK. Identification of ketone 104 as 3,4-secocholestane-6-one-(3α,5α)(3β,4)-dioxide Journal of the American Chemical Society. 82: 1700-1706. DOI: 10.1021/Ja01492A044 |
0.353 |
|
1960 |
Fieser LF, Goto T. Anhydro derivatives of strophanthidin Journal of the American Chemical Society. 82: 1697-1700. DOI: 10.1021/Ja01492A043 |
0.397 |
|
1960 |
Fieser LF, Goto T. Oxido alcohols and ketoxides Journal of the American Chemical Society. 82: 1693-1697. DOI: 10.1021/Ja01492A042 |
0.342 |
|
1960 |
Fieser LF, Huang WY, Goto T. Origin of ketone 104 and isolation of a companion acid Journal of the American Chemical Society. 82: 1688-1693. DOI: 10.1021/Ja01492A041 |
0.399 |
|
1959 |
Goto T, Fieser LF. B-Norcoprostane Derivatives Journal of the American Chemical Society. 81: 2276-2277. DOI: 10.1021/Ja01518A072 |
0.373 |
|
1957 |
Shimomura O, Goto T, Hirata Y. Crystalline Cypridina Luciferin Bulletin of the Chemical Society of Japan. 30: 929-933. DOI: 10.1246/Bcsj.30.929 |
0.348 |
|
1957 |
Goto T, Hirata Y, Hosoya S, Komatsu N. Structure of Roseothricin A Bulletin of the Chemical Society of Japan. 30: 729-737. DOI: 10.1246/Bcsj.30.729 |
0.425 |
|
1957 |
Goto T, Hirata Y, Hosoya S, Komatsu N. Structure of Compound A, α Hydrolysis Product of Roseothricin A Bulletin of the Chemical Society of Japan. 30: 304-305. DOI: 10.1246/Bcsj.30.304 |
0.433 |
|
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