Issue 57, 2015

I2/Cu-mediated self-sorting domino reaction of aryl β-ketoesters into symmetrical 2-carboalkoxy-1,4-enediones: application to synthesis of pyrazine, β-carboline and quinoxalines

Abstract

A self-sorting domino reaction of aryl β-ketoesters into symmetrical 1,4-enediones is reported by an I2/Cu system. The reaction proceeds through tandem iodination, self-dimerization and Krapcho dealkoxycarbonylation in one pot under open air condition. Further, 1,4-enediones were successfully employed for the synthesis of bioactive pyrazine, β-carboline and quinoxalines via aza-Michael addition, intramolecular cyclization and C–C bond cleavage of 1,3-dicarbonyl unit under mild reaction condition.

Graphical abstract: I2/Cu-mediated self-sorting domino reaction of aryl β-ketoesters into symmetrical 2-carboalkoxy-1,4-enediones: application to synthesis of pyrazine, β-carboline and quinoxalines

Supplementary files

Article information

Article type
Paper
Submitted
01 May 2015
Accepted
18 May 2015
First published
18 May 2015

RSC Adv., 2015,5, 46163-46172

Author version available

I2/Cu-mediated self-sorting domino reaction of aryl β-ketoesters into symmetrical 2-carboalkoxy-1,4-enediones: application to synthesis of pyrazine, β-carboline and quinoxalines

G. Satish and A. Ilangovan, RSC Adv., 2015, 5, 46163 DOI: 10.1039/C5RA08030D

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