DEVELOPMENT OF A NEW N^π-PROTECTING GROUP FOR HISTIDINE, N^π-1-ADAMANTYLOXYMETHYLSHISTIDINE
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概要
- 論文の詳細を見る
N^π-1-Adamantyloxymethylhistidine, His(N^π-1-Adom) was prepared, and the properties of the 1-Adom group were examined. 1-Adom group can be easily removed by TFA ; it is stable to 20% piperidine/DMF and 1N NaOH. His(N^π-1-Adom) derivatives can suppress racemization during coupling reaction. TRH was synthesized using His(N^π-1-Adom), successfully.
- 公益社団法人日本薬学会の論文
- 1996-04-15
著者
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OKADA Yoshio
Faculty of Pharmaceutical Sciences, Kobe Gakuin University
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Okada Yoshio
Faculty Of Pharmaceutical Sciences Kobe Gakuin University
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YOKOI Toshio
The Graduate School of Food and Medicinal Sciences, Kobe Gakuin University
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MU Yu
Faculty of Pharmaceutical Sciences, Osaka University
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Mu Y
Faculty Of Pharmaceutical Sciences Kobe Gakuin University
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Mu Yu
Faculty Of Pharmaceutical Sciences Kobe Gakuin University
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Wang J
Shenyang Pharmaceutical Univ. Shenyang Chn
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Yokoi T
Faculty Of Pharmaceutical Sciences And High-technology Research Center Kobe-gakuin University
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Yokoi T
Kobe‐gakuin Univ. Hyogo Jpn
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YAMAMOTO Takeshi
Faculty of Engineering, Kobe University
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Yamamoto T
R&d Laboratories Nippon Organon K.k.
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WANG Jidong
Faculty of Pharmaceutical Sciences, Kobe Gakuin University
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Wang J
Department Of Synchrotron Radiation Science The Graduate University For Advanced Studies
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Yokoi T
Fucunlty Of Pharmaceutical Sciences Kobe Gakuin University
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Yamamoto Takeshi
Faculty Of Agriculture Kochi University
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