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通过铜催化的烯基肟的多米诺环化/氰化反应来获得含氰基异恶唑啉。

Access to Cyano-Containing Isoxazolines via Copper-Catalyzed Domino Cyclization/Cyanation of Alkenyl Oximes.

机构信息

Jiangsu Key Laboratory of Pesticide Science and Department of Chemistry, College of Sciences, Nanjing Agricultural University , Nanjing 210095, P. R. China.

出版信息

J Org Chem. 2017 Oct 6;82(19):10742-10747. doi: 10.1021/acs.joc.7b02133. Epub 2017 Sep 26.

Abstract

A highly efficient copper-catalyzed cyclization/cyanation cascade of unactivated olefins bearing oximes is described. A variety of cyano-containing isoxazolines have been obtained in high yields with cheap Cu(NO)·3HO as the catalyst and TMSCN as the non-metallic cyanide source. The present method provides a mild, simple, and practical access to cyano-substituted isoxazolines and is amenable to gram scale. The simultaneous construction of C(sp)-CN and C-O bonds can be achieved in one step.

摘要

描述了一种高效的铜催化未活化肟取代烯烃的环化/氰化级联反应。以廉价的硝酸铜和 TMSCN 作为催化剂和非金属氰源,多种氰基取代的异恶唑啉以高产率得到。该方法提供了一种温和、简单、实用的氰基取代异恶唑啉的合成方法,适用于克级规模。可以一步实现 C(sp)-CN 和 C-O 键的同时构建。

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