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通过偕二氟烯烃与α,β-不饱和羰基化合物的光催化串联环化反应实现单氟环己烯的非对映选择性合成。

Diastereoselective Synthesis of Monofluorocyclohexenes through Photocatalyzed Cascade Cyclization of gem-Difluoroalkenes and α,β-Unsaturated Carbonyl Compounds.

作者信息

Li Zhengyu, Zhang Yizhi, Zhang Yunxiao, He Xingyi, Shen Xiao

机构信息

Institute for Advanced Studies, Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, Wuhan University, 299 Bayi Road, Wuhan, Hubei, 430072, China.

Shenzhen Research Institute of Wuhan University, Shenzhen, 518057, China.

出版信息

Angew Chem Int Ed Engl. 2023 May 8;62(20):e202303218. doi: 10.1002/anie.202303218. Epub 2023 Apr 12.

Abstract

Monofluoroalkenes are nonhydrolyzable mimetics of amides. Previous work focused on the synthesis of non-cyclic monofluoroalkenes. However, diastereoselective synthesis of monofluorocyclohexenes from non-cyclic substrates is challenging. Herein, we report the first photocatalyzed cascade cyclization reactions of readily available α,β-unsaturated carbonyl compounds and gem-difluoroalkenes for the synthesis of highly functionalized monofluorocyclohexenes. The reaction shows broad substrate scope with high diastereoselectivity (>30 examples, up to 86 % yield, >20 : 1 dr). The post-reaction transformations of the products demonstrate the synthetic potential of this methodology.

摘要

单氟烯烃是酰胺的不可水解模拟物。先前的工作集中在非环状单氟烯烃的合成上。然而,从非环状底物非对映选择性合成单氟环己烯具有挑战性。在此,我们报道了首例光催化的级联环化反应,该反应以易得的α,β-不饱和羰基化合物和偕二氟烯烃为原料,用于合成高度官能化的单氟环己烯。该反应底物范围广泛,具有高非对映选择性(>30个例子,产率高达86%,非对映体比例>20:1)。产物的反应后转化证明了该方法的合成潜力。

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