Functionalization of Polymethylcarboranes. Preparation and Reactivity of 2,3,4,5,6,7,8,9,10,11-Decamethyl-1,12-dicarba-closo-dodecaborane(12)-1-carboxylic Acid
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概要
- 論文の詳細を見る
The preparation and reactivity of poly-B-methyl-1,12-dicarba-closo-dodecaborane (poly-B-methyl-p-carborane) derivatives are described. 2,3,4,5,6,7,8,9,10,11-Decamethyl-1,12-dicarba-closo-dodecaborane(12)-1-carboxylic acid was prepared from 2,3,4,5,6,7,8,9,10,11-decamethyl-1,12-decarba-closo-dodecaborane(12) by lithiation with methyllithium, followed by carboxylaiton. Conversion of the carboxylic acid into its ester and amide were achieved through its acyl chloride. The ester and the amide could not be hydrolyzed due to severe steric hindrance around the carbonyl group of the molecules owing to the adjacent B-methyl groups.
- 社団法人日本薬学会の論文
- 1999-05-15
著者
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遠藤 泰之
東北薬科大学薬学部
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YAMAGUCHI KENTARO
Chemical Analytical Center, Chiba University
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Shudo Koichi
Graduate School Of Pharmaceutical Sciences The University Of Tokyo
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ENDO Yasuyuki
Graduate School of Pharmaceutical Sciences, The University of Tokyo
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YAGUCHI Kyoko
Graduate School of Pharmaceutical Sciences, University of Tokyo
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TSUJI Motonori
Graduate School of Pharmaceutical Sciences, University of Tokyo
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Shudo K
Research Foundation Itsuu Laboratory
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Yamaguchi Kentaro
Chemical Analysis Center Chiba University
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Yaguchi Kyoko
Graduate School Of Pharmaceutical Sciences University Of Tokyo
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Tsuji M
Univ. Tokyo Tokyo Jpn
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Tsuji Motonori
Graduate School Of Pharmaceutical Sciences University Of Tokyo
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Endo Yasuyuki
Graduate School Of Pharmaceutical Sciences University Of Tokyo
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Yamaguchi Kentaro
Chemical Analysis Center Chiba Univ. Chiba 263-8522 Jpn
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