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首页> 外文期刊>Angewandte Chemie >Highly Regio- and Enantioselective Synthesis of gamma,delta-Unsaturated Amido Esters by Catalytic Hydrogenation of Conjugated Enamides
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Highly Regio- and Enantioselective Synthesis of gamma,delta-Unsaturated Amido Esters by Catalytic Hydrogenation of Conjugated Enamides

机译:共轭酰胺的催化加氢对γ,δ-不饱和酰胺基酯的高度区域和对映选择性合成

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摘要

An efficient and highly regio- and enantioselective catalytic asymmetric hydrogenation of ,-dienamido esters to ,-unsaturated amido esters has been achieved using Rh/TangPhos as the catalyst. A series of ,-unsaturated amido acids were furnished in excellent yields with up to 99% ee. This effective methodology was applied in the asymmetric synthesis of key intermediate of Ramipril, an ACE inhibitor.
机译:使用Rh / TangPhos作为催化剂,已实现了高效的,高区域选择性和对映选择性的不对称加氢反应,将β-二酰胺基酯合成为α-不饱和酰胺基酯。以极高的产率提供了一系列99%ee的不饱和酰胺酸。这种有效的方法应用于ACE抑制剂雷米普利的关键中间体的不对称合成。

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