首页> 外文期刊>Advanced synthesis & catalysis >Oxidative Heck Coupling of Allylic Amines with 2,2,6,6-Tetramethylpiperidine-N-oxyl (TEMPO) as Oxidant for the Preparation of Tetrasubstituted Alkenes
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Oxidative Heck Coupling of Allylic Amines with 2,2,6,6-Tetramethylpiperidine-N-oxyl (TEMPO) as Oxidant for the Preparation of Tetrasubstituted Alkenes

机译:以2,2,6,6-四甲基哌啶-N-氧基(TEMPO)为氧化剂的烯丙基胺的氧化Heck偶联制备四取代的烯烃

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摘要

The paper describes the oxidative Heck ar-ylation of various allylic amines using arylboronic acids for the preparation of tetrasubstituted alkenes. As oxidant the commercially available 2,2,6,6-tetra-methylpiperidine-N-oxyl (TEMPO) is used and coupling reactions occur under very mild conditions at room temperature. The densely substituted alkenes are formed in good to excellent yields with complete control of the diastereoselectivity. Substrate scope with respect to the allylic amine and the arylboronic acid is investigated.
机译:该论文描述了使用芳基硼酸制备四取代烯烃时各种烯丙基胺的氧化Heck烷基化反应。作为氧化剂,使用可商购的2,2,6,6-四甲基哌啶-N-氧基(TEMPO),偶联反应在非常温和的室温条件下发生。在完全控制非对映选择性的情况下,以良好或优异的收率形成了稠密取代的烯烃。研究了关于烯丙基胺和芳基硼酸的底物范围。

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