Studies on Oxytetracycline and Related Compounds. XIII. Synthesis and Stereoisomers of (α-Methylbenzyl) succinic Acid. (2).
スポンサーリンク
概要
- 論文の詳細を見る
The configuration of the diastereoisomers, (Ia) and (Ib), of (α-methylbenzyl) succinic acid was determined by preparing them by the cis-reduction of cis- and trans-(α-methylbenzylidene) succinic acid, (IIa) and (IIb). It was also found that the Schwenk-Papa reduction of (IIa) and (IIb) proceeded stereospecifically and cis-addition of hydrogen to the double bond was observed. This stereospecificity of the reduction was further confirmed in other cases.
- 公益社団法人日本薬学会の論文
- 1961-06-25
著者
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堀井 善一
School of Pharmacy, Osaka University
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田村 恭光
School of Pharmacy, Osaka University
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酒井 立夫
Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University
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酒井 立夫
School of Pharmacy, University of Osaka
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