Palladium-catalyzed Suzuki-Miyaura cross-couplings of sulfonyl chlorides and boronic acids
Dubbaka, S. R.; Vogel, P.
2004

Abstract

Arene-, arylmethane, and alk-2-ene-1-sulfonyl chlorides undergo Suzuki-Miyaura cross-coupling with arene-, heteroarene-, and alkeneboronic acids in THF at reflux. The reactivity order is Arl > ArSO2Cl > ArBr much greater than ArCl.

Details

Title Palladium-catalyzed Suzuki-Miyaura cross-couplings of sulfonyl chlorides and boronic acids
Author(s) Dubbaka, S. R. ; Vogel, P.
Published in Organic Letters
Volume 6
Issue 1
Pages 95-98
Date 2004
ISSN 1523-7060
Keywords
Note Swiss Fed Inst Technol, Inst Mol & Biol Chem, BCH, CH-1015 Lausanne, Switzerland.
DOI https://doi.org/10.1021/ol036131x
Other identifier(s) DAR: 4603
View record in Web of Science
Laboratories LGSA
Record Appears in Scientific production and competences > SB - School of Basic Sciences > SB Archives > LGSA - Laboratory of Glycochemistry and Asymmetric Synthesis
Peer-reviewed publications
Work produced at EPFL
Journal Articles
Published
Record creation date 2005-11-09

Actions