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氰基引入反应:镍催化氰醇与醛/酮直接转化为β-氰基酮。

Cyano-borrowing reaction: nickel-catalyzed direct conversion of cyanohydrins and aldehydes/ketones to β-cyano ketone.

作者信息

Li Zhao-Feng, Li Qian, Ren Li-Qing, Li Qing-Hua, Peng Yun-Gui, Liu Tang-Lin

机构信息

School of Chemistry and Chemical Engineering , Southwest University , Chongqing 400715 , China . Email:

出版信息

Chem Sci. 2019 May 6;10(22):5787-5792. doi: 10.1039/c9sc00640k. eCollection 2019 Jun 14.

Abstract

A direct nickel-catalyzed, high atom- and step-economical reaction of cyanohydrins with aldehydes or ketones an unprecedented "cyano-borrowing reaction" has been developed. Cleavage of the C-CN bond of cyanohydrins followed by aldol condensation and conjugate addition of cyanide to α,β-unsaturated ketones proceeded to deliver a range of racemic β-cyano ketones with good to high yields. The practical procedure with the use of a commercial and less-toxic CN source bodes well for wide application of this protocol.

摘要

已开发出一种直接镍催化的、具有高原子经济性和步骤经济性的氰醇与醛或酮的反应——一种前所未有的“氰基转借反应”。氰醇的C-CN键断裂,随后进行羟醛缩合以及氰化物对α,β-不饱和酮的共轭加成,从而以良好至高收率得到一系列外消旋β-氰基酮。使用商业且毒性较小的氰源的实用方法预示着该方案将得到广泛应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d3/6568282/098c2719c09c/c9sc00640k-s1.jpg

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