Issue 9, 2015

Synthesis of aromatic β-keto esters via a carbonylative Suzuki–Miyaura coupling reaction of α-iodo esters with arylboronic acids

Abstract

Aromatic β-keto esters were synthesized via a carbonylative cross-coupling reaction of alkyl iodides and arylboronic acids in the presence of a catalytic amount of Pd catalyst. A cooperative radical and Pd-catalyzed mechanism is proposed.

Graphical abstract: Synthesis of aromatic β-keto esters via a carbonylative Suzuki–Miyaura coupling reaction of α-iodo esters with arylboronic acids

Supplementary files

Article information

Article type
Research Article
Submitted
10 Jun 2015
Accepted
13 Jul 2015
First published
14 Jul 2015

Org. Chem. Front., 2015,2, 1085-1087

Author version available

Synthesis of aromatic β-keto esters via a carbonylative Suzuki–Miyaura coupling reaction of α-iodo esters with arylboronic acids

S. Sumino, T. Ui and I. Ryu, Org. Chem. Front., 2015, 2, 1085 DOI: 10.1039/C5QO00185D

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