Issue 27, 2019

Visible-light-induced deboronative alkylarylation of acrylamides with organoboronic acids

Abstract

A visible-light-induced deboronative alkylarylation of acrylamides with organoboronic acids was developed. In this transformation, boronic acids could be activated by the organic photocatalyst of eosin Y, generating alky free radicals in high efficiency. A broad range of substrate scope was examined and a number of 3,3-disubstituted oxindoles were synthesized in high yields.

Graphical abstract: Visible-light-induced deboronative alkylarylation of acrylamides with organoboronic acids

Supplementary files

Article information

Article type
Paper
Submitted
04 May 2019
Accepted
15 Jun 2019
First published
17 Jun 2019

Org. Biomol. Chem., 2019,17, 6612-6619

Visible-light-induced deboronative alkylarylation of acrylamides with organoboronic acids

X. Li, M. Han, B. Wang, L. Wang and M. Wang, Org. Biomol. Chem., 2019, 17, 6612 DOI: 10.1039/C9OB01023H

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