Issue 44, 2018

Rh-Catalyzed C–H bond alkylation of indoles with α,α-difluorovinyl tosylate via indolyl group migration

Abstract

Herein we demonstrate that an alkylation of indoles could be accessed through C–H bond functionalization with α,α-difluorovinyl tosylate. The key aspect for the effective alkylation is the influence of the fluorine substituents on the reactivity of the C[double bond, length as m-dash]C double bond, allowing regioselective insertion as well as an indolyl group shift process. Furthermore, the fluorides are removed through alcoholysis to furnish the alkylation product as a traceless auxiliary.

Graphical abstract: Rh-Catalyzed C–H bond alkylation of indoles with α,α-difluorovinyl tosylate via indolyl group migration

Supplementary files

Article information

Article type
Communication
Submitted
19 Mar 2018
Accepted
04 May 2018
First published
05 May 2018

Chem. Commun., 2018,54, 5618-5621

Rh-Catalyzed C–H bond alkylation of indoles with α,α-difluorovinyl tosylate via indolyl group migration

L. Zhou, C. Zhu, T. Loh and C. Feng, Chem. Commun., 2018, 54, 5618 DOI: 10.1039/C8CC02183J

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