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铑(I)催化的乙烯基氮丙啶和炔烃的分子间环加成反应合成氮杂环化合物的多样性。

The Divergent Synthesis of Nitrogen Heterocycles by Rhodium(I)-Catalyzed Intermolecular Cycloadditions of Vinyl Aziridines and Alkynes.

机构信息

Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University , 3663 N. Zhongshan Road, Shanghai 200062, P. R. China.

出版信息

J Am Chem Soc. 2016 Feb 24;138(7):2178-81. doi: 10.1021/jacs.6b00386. Epub 2016 Feb 15.

Abstract

Catalyst-controlled divergent intermolecular cycloadditions of vinylaziridines with alkynes have been developed. By using [Rh(NBD)2]BF4 as the catalyst, a [3 + 2] cycloaddition reaction was achieved with broad substrate scope and high stereoselectivity under mild reaction conditions. Moreover, the chirality of vinylaziridines can be completely transferred to the [3 + 2] cycloadducts. When the catalyst was changed to [Rh(η(6)-C10H8) (COD)]SbF6, the alternative [5 + 2] cycloadducts were selectively formed under otherwise identical conditions.

摘要

已开发出乙烯基氮丙啶与炔烃的催化剂控制的发散分子间环加成反应。使用[Rh(NBD)2]BF4 作为催化剂,在温和的反应条件下,通过广泛的底物范围和高立体选择性实现了[3+2]环加成反应。此外,乙烯基氮丙啶的手性可以完全转移到[3+2]环加成产物中。当催化剂变为[Rh(η(6)-C10H8)(COD)]SbF6 时,在其他条件相同的情况下,选择性地形成了替代的[5+2]环加成产物。

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