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Sc(OTf) 催化的全氟烷基化 3-吲哚甲醇的 C2-选择性氰化/脱氟级联反应及在 3-氟(全氟烷基)-β-咔啉合成中的应用。

Sc(OTf)-Catalyzed C2-Selective Cyanation/Defluorination Cascade of Perfluoroalkylated 3-Indolylmethanols and Application to the Synthesis of 3-Fluoro(perfluoroalkyl)-β-carbolines.

机构信息

Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources, Jiangsu Key Lab of Biomass-Based Green Fuels and Chemicals, College of Chemical Engineering, Nanjing Forestry University, Nanjing, 210037, China.

出版信息

Org Lett. 2021 Oct 1;23(19):7666-7671. doi: 10.1021/acs.orglett.1c02932. Epub 2021 Sep 20.

Abstract

An unprecedented Sc(OTf)-catalyzed C2-selective cyanation/defluorination cascade of perfluoroalkylated 3-indolylmethanols with TMSCN is described, which provides a novel and practical strategy for the synthesis of structurally diverse 3-(2-cyano)-indolyl substituted -difluoroalkenes and β-fluoro-β-perfluoroalkylalkenes. The reaction features excellent regio- and stereoselectivity and broad substrate scope. Notably, the obtained -difluoroalkenes and β-fluoro-β-perfluoroalkylalkenes could be easily transformed into 3-fluoro(perfluoroalkyl)-β-carbolines with excellent efficiency simply by treating them with Grignard reagents or DIBAL-H under mild reaction conditions.

摘要

本文描述了一种史无前例的 Sc(OTf)-催化的全氟烷基化 3-吲哚甲醇与 TMSCN 的 C2 选择性氰化/脱氟级联反应,为合成结构多样的 3-(2-氰基)-吲哚基取代的 -二氟烯烃和β-氟-β-全氟烷基烯烃提供了一种新颖实用的策略。该反应具有优异的区域和立体选择性以及广泛的底物范围。值得注意的是,通过在温和的反应条件下用格氏试剂或 DIBAL-H 处理,所得的 -二氟烯烃和β-氟-β-全氟烷基烯烃可以很容易地转化为 3-氟(全氟烷基)-β-咔啉,收率极好。

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