Issue 5, 2017

Oxidative decarbonylative coupling of aliphatic aldehydes with methacryloyl benzamides to generate isoquinoline-1,3(2H,4H)-diones

Abstract

Alkyl-substituted isoquinoline-1,3(2H,4H)-diones were prepared by decarbonylative coupling of N-alkyl-N-methacryloylbenzamides and aliphatic aldehydes under metal-free conditions. The reaction undergoes subsequent decarbonylation, radical addition and cyclization processes with aliphatic aldehydes as the cheap and abundant alkyl radical source. This procedure offers a complementary approach to the convenient generation of alkyl-substituted isoquinoline-1,3(2H,4H)-diones.

Graphical abstract: Oxidative decarbonylative coupling of aliphatic aldehydes with methacryloyl benzamides to generate isoquinoline-1,3(2H,4H)-diones

Supplementary files

Article information

Article type
Communication
Submitted
18 Nov 2016
Accepted
19 Dec 2016
First published
09 Jan 2017

Org. Biomol. Chem., 2017,15, 1096-1099

Oxidative decarbonylative coupling of aliphatic aldehydes with methacryloyl benzamides to generate isoquinoline-1,3(2H,4H)-diones

C. Pan, C. Chen and J. Yu, Org. Biomol. Chem., 2017, 15, 1096 DOI: 10.1039/C6OB02533A

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