Purines. XXVIII. Preparation of Some 3,7-Dialkyladenines from 3-Alkyladenines by Alkylation : A Subordinate Formation of 3,9-Dialkyladenines
スポンサーリンク
概要
- 論文の詳細を見る
A detailed account is given of the preferential alkylation at the 7-position of 3-alkyladenines (1-3), which has been effected with MeI, EtI, and PhCH_2Br in AcNMe_2 or acetone to prepare the corresponding 3,7-dialkyladenine salts (4a-i). In the cases of benzylation of 3-methyladenine (1) and 3-ethyladenine (2) and methylation of 3-benzyladenine (3), the 9-position has been found to be another, but much less favored site of alkylation.
- 公益社団法人日本薬学会の論文
- 1986-04-25
著者
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斎藤 徹
Faculty Of Pharmaceutical Sciences Kanazawa University
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井上 勲
Faculty Of Pharmaceutical Sciences Kanazawa University
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藤井 澄三
Faculty Of Pharmaceutical Sciences Kanazawa University
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Leonard N
School Of Chemical Sciences University Of Illinois
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熊澤 幸成
Faculty of Pharmaceutical Sciences, Kanazawa University
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LEONARD NELSON
School of Chemical Sciences, University of Illinois
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藤井 澄三
Shinshu Univ. Nagano Jpn
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熊澤 幸成
Faculty Of Pharmaceutical Sciences Kanazawa University
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