Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Toshishige Inui"'
Autor:
Takeo Kaneko, Toshishige Inui
Publikováno v:
Nippon kagaku zassi. 82:1078-1081
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb6d52b09d32bb3155ab918691d4c5a2
https://doi.org/10.1246/nikkashi1948.82.8_1078
https://doi.org/10.1246/nikkashi1948.82.8_1078
Autor:
Toshishige Inui, Takeo Kaneko
Publikováno v:
Nippon kagaku zassi. 82:1075-1078
オキシアミノ酸はべンジルオキシカルボニルク糧リドを炭酸水素ナトリウムの存在で作用させると通常の N-ペンジルオキシカルボニル誘導体を生成するが,水酸化ナトリウムの存在では閉
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5524c8031d0b0d3daa199b5fbae57138
https://doi.org/10.1246/nikkashi1948.82.8_1075
https://doi.org/10.1246/nikkashi1948.82.8_1075
Autor:
Max Safdy, Roger A. Upham, Toshishige Inui, Warren C. Jun. Jones, Richard G. Hiskey, Gerald E. Davis
Publikováno v:
The Journal of Organic Chemistry. 35:4148-4156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a9f87e19806b651ee3c9e7b600eccd3
https://doi.org/10.1021/jo00837a603
https://doi.org/10.1021/jo00837a603
Publikováno v:
The Journal of Organic Chemistry. 31:1192-1195
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c93130dce8b5f3764d92b0b4fa231e85
https://doi.org/10.1021/jo01342a049
https://doi.org/10.1021/jo01342a049
Publikováno v:
Bulletin of the Chemical Society of Japan. 41:2155-2161
Threonine peptide was converted to an oxazolidone derivative via an O-chlorocarbonyl derivative by treatment with phosgene and dimethylaniline followed by refluxing in xylene, wherever the threonin...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c3ba9c77ceb9e128801628ca66427b4
https://doi.org/10.1246/bcsj.41.2155
https://doi.org/10.1246/bcsj.41.2155
Publikováno v:
Bulletin of the Chemical Society of Japan. 41:974-979
The treatment of N-benzyloxycarbonyl-L-alanyl-L-serine methyl ester (I) with phosgene afforded the corresponding O-chlorocarbonyl derivative (II), which was then cyclized to methyl L-3-(N-benzyloxycarbonyl-L-alanyl)-2-oxo-oxazolidine-4-carboxylate (I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdbb097b18310845582cde163d48034a
https://doi.org/10.1246/bcsj.41.974
https://doi.org/10.1246/bcsj.41.974
Autor:
Takeo Kaneko, Toshishige Inui
Publikováno v:
Bulletin of the Chemical Society of Japan. 35:1145-1149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e951260aa61aa3fe9ced68a5a863c4ff
https://doi.org/10.1246/bcsj.35.1145
https://doi.org/10.1246/bcsj.35.1145
Autor:
Toshishige Inui
Publikováno v:
Bulletin of the Chemical Society of Japan. 44:2515-2520
The cysteine peptides such as IV were cyclized to thiazolidone peptides through the corresponding S-chlorocarbonyl derivatives. In some peptides such as XXII, however, no cyclized products were isolated because of decomposition of the S-chlorocarbony
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b97932d3b2ad46766b58dcb07f71e7a0
https://doi.org/10.1246/bcsj.44.2515
https://doi.org/10.1246/bcsj.44.2515
Autor:
Toshishige Inui, Masazumi Nakagawa
Publikováno v:
Nippon kagaku zassi. 73:143-145
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d4200fdc4569a89d8790ad4cd527ab1
https://doi.org/10.1246/nikkashi1948.73.143
https://doi.org/10.1246/nikkashi1948.73.143
Publikováno v:
Bulletin of the Chemical Society of Japan. 43:1582-1584
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36b65e24d3ffa433bc0c47a81b531cb0
https://doi.org/10.1246/bcsj.43.1582
https://doi.org/10.1246/bcsj.43.1582