Experts has a new look! Let us know what you think of the updates.

Provide feedback
Home
Scholarly Works
Efficient palladium-catalysed carbonylative and...
Journal article

Efficient palladium-catalysed carbonylative and Suzuki–Miyaura cross-coupling reactions with bis(di-tert-butylphosphino)-o-xylene

Abstract

The use of the ligand bis(di-tert-butylphosphino)-o-xylene (dtbpx) in palladium-catalysed carbonylative and Suzuki–Miyaura cross-coupling reactions is described. Aryl and vinyl halides readily entered into the carbonylative catalytic cycle affording carboxylic acids, amides as well as primary, secondary and tertiary esters, respectively, in good yields. Aryl iodides, bromides and chlorides gave high yields of biphenyl products upon reaction …

Authors

McNulty J; Nair JJ; Sliwinski M; Robertson AJ

Journal

Tetrahedron Letters, Vol. 50, No. 20, pp. 2342–2346

Publisher

Elsevier

Publication Date

May 2009

DOI

10.1016/j.tetlet.2009.02.200

ISSN

0040-4039