Issue 78, 2017, Issue in Progress

Visible-light induced tandem radical cyanomethylation and cyclization of N-aryl acrylamides: access to cyanomethylated oxindoles

Abstract

A visible-light induced cyanomethylation of N-aryl acrylamides with bromoacetonitrile followed by intramolecular cyclization has been explored. This transformation exhibits a wide substrate scope and significant functional group tolerance, providing a facile synthetic approach and highly efficient access to cyanomethylated oxindoles.

Graphical abstract: Visible-light induced tandem radical cyanomethylation and cyclization of N-aryl acrylamides: access to cyanomethylated oxindoles

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2017
Accepted
16 Oct 2017
First published
23 Oct 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 49299-49302

Visible-light induced tandem radical cyanomethylation and cyclization of N-aryl acrylamides: access to cyanomethylated oxindoles

X. Gao, W. Dong, B. Hu, H. Gao, Y. Yuan, X. Xie and Z. Zhang, RSC Adv., 2017, 7, 49299 DOI: 10.1039/C7RA10090F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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