用o -酰基羟胺催化烯丙基胺化:直接进入多种n -烷基烯丙胺

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL
Eric J. McLaren, Guangshou Feng, Noah H. Watkins, Qiu Wang
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引用次数: 0

摘要

我们报告了一个铜催化烯烃的直接烯丙基胺化,使用现成的邻苯并羟胺作为烷基胺前体和内部氧化剂。一系列的伯烷基胺和仲烷基胺可以安装在不同取代的烯烃上,以快速构建n -烷基烯丙胺。机理研究表明,该反应的初始亲电胺化反应具有反马尔可夫尼科夫选择性,随后是区域选择性氧化消除,以提供双键转位。在亲电胺化步骤中,使用强Brønsted酸对于生成关键的胺基阳离子(ARC)物种至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Copper-Catalyzed Allylic Amination of Alkenes Using O-Acylhydroxylamines: A Direct Entry to Diverse N-Alkyl Allylamines

Copper-Catalyzed Allylic Amination of Alkenes Using O-Acylhydroxylamines: A Direct Entry to Diverse N-Alkyl Allylamines
We report a copper-catalyzed direct allylic amination of alkenes using readily available O-benzyolhydroxylamines as the alkylamine precursors and internal oxidant. A range of primary and secondary alkylamines can be installed onto diversely substituted alkenes for the rapid construction of N-alkyl allylamines. Mechanistic studies support that the reaction engages an initial electrophilic amination to alkenes with anti-Markovnikov selectivity and subsequently a regioselective oxidative elimination to furnish the double bond transposition. In the electrophilic amination step, the use of strong Brønsted acid is critical for generating the key aminium radical cation (ARC) species.
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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