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Stereoselective Synthesis of (Z)-2-Acylamido-4-phenylcrotonates
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作者 Yi Nong XIE fan min fu +1 位作者 Ai Qiao MI Yao Zhong JIANG(Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences,Chengdu 610041) 《Chinese Chemical Letters》 SCIE CAS CSCD 2000年第7期567-570,共4页
Two practical methods for highly stereoselective synthesis of (Z)-2-acylamido-4-phenylcrotonates 2a similar to b have been developed. The key step in the first route was how to control the acid-catalyzed isomerization... Two practical methods for highly stereoselective synthesis of (Z)-2-acylamido-4-phenylcrotonates 2a similar to b have been developed. The key step in the first route was how to control the acid-catalyzed isomerization of condensation mixtures of alpha-keto ester 5 with carbomite. In the second route the key step was reduction of oxime 8, derived from alpha-keto ester 5, with iron powder in the presence of acetic anhydride. 展开更多
关键词 (Z)-alpha beta-dehydroamino acids stereoselective synthesis E -> Z isomerization Fe/Ac2O reduction of oxime
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