Issue 57, 2016, Issue in Progress

Propargylation of 1,3-dicarbonyl compounds catalyzed by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and sodium nitrite in the presence of molecular oxygen and formic acid

Abstract

Catalyzed by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and sodium nitrite, the coupling reaction of 1,3-diarylpropynes and 1,3-dicarbonyl compounds using molecular oxygen as a terminal oxidant was developed. The reaction was promoted dramatically in the presence of HCOOH. The corresponding products were obtained within half an hour in 37–87% yields.

Graphical abstract: Propargylation of 1,3-dicarbonyl compounds catalyzed by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and sodium nitrite in the presence of molecular oxygen and formic acid

Supplementary files

Article information

Article type
Communication
Submitted
15 Mar 2016
Accepted
12 May 2016
First published
24 May 2016

RSC Adv., 2016,6, 52459-52463

Propargylation of 1,3-dicarbonyl compounds catalyzed by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and sodium nitrite in the presence of molecular oxygen and formic acid

D. Cheng, X. Zhou, X. Xu and J. Yan, RSC Adv., 2016, 6, 52459 DOI: 10.1039/C6RA06704B

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