首页> 外文期刊>Angewandte Chemie >Regio- and Stereoselective Construction of gamma-Butenolides through Phosphine-Catalyzed Substitution of Morita-Baylis-Hillman Acetates:An Organocatalytic Allylic Alkylation
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Regio- and Stereoselective Construction of gamma-Butenolides through Phosphine-Catalyzed Substitution of Morita-Baylis-Hillman Acetates:An Organocatalytic Allylic Alkylation

机译:通过膦催化的森田-贝利斯-希尔曼醋酸酯的γ-丁烯内酯的区域和立体选择性构建:有机催化的烯丙基烷基化

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摘要

The gamma-butenolide ring system ranks among the most ubiquitous structural motifs found in naturally occurring organic molecules.Owing to the prevalence of gamma-butenolides,their regio- and Stereoselective synthesis has been the focus of intensive effort.In this regard,the use of 2-silyloxy furans as nucleophilic partners in Mukaiyama-aldol-,Mukaiyama-Michael-,and Mukaiyama-Mannich-type additions has emerged as an effective strategy.Even broader access to butenolide substructures would be possible through the development of new electrophilic partners amenable to 2-silyloxy furan addition.
机译:γ-丁烯内酯环系统是天然存在的有机分子中最普遍存在的结构基序。由于γ-丁烯内酯的普遍性,其区域和立体选择性合成一直是研究的重点。在这方面,使用在Mukaiyama-aldol-,Mukaiyama-Michael-和Mukaiyama-Mannich型添加物中,作为亲核伙伴的2-甲硅烷氧基呋喃已经成为一种有效的策略。通过开发适合于人类的新的亲电子伙伴,甚至可以更广泛地使用丁烯内酯亚结构。 2-甲硅烷氧基呋喃加成。

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