Issue 19, 2003

Rhodium-catalyzed Heck-type reaction of arylboronic acids with α,β-unsaturated esters: tuning β-hydrogen elimination vs.hydrolysis of alkylrhodium species

Abstract

The elusive rhodium-catalyzed Heck-type coupling of arylboronic acids with α,β-unsaturated esters is effected using rhodium chloride as catalyst, indicating the hydrolysis of Rh–C bond could be finely tuned by the steric environment around rhodium.

Graphical abstract: Rhodium-catalyzed Heck-type reaction of arylboronic acids with α,β-unsaturated esters: tuning β-hydrogen elimination vs. hydrolysis of alkylrhodium species

Article information

Article type
Communication
Submitted
22 May 2003
Accepted
12 Aug 2003
First published
20 Aug 2003

Chem. Commun., 2003, 2438-2439

Rhodium-catalyzed Heck-type reaction of arylboronic acids with α,β-unsaturated esters: tuning β-hydrogen elimination vs. hydrolysis of alkylrhodium species

G. Zou, Z. Wang, J. Zhu and J. Tang, Chem. Commun., 2003, 2438 DOI: 10.1039/B305771M

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