Efficient aqueous-phase Suzuki coupling of activated aryl chlorides with arylboronic acids using d-glucosamine-based dicyclohexylarylphosphine

[Display omitted] The synthesis of a new d-glucosamine-based dicyclohexylarylphosphine has been developed. The catalytic performance of this neutral ligand is demonstrated in the Suzuki–Miyaura cross-coupling reaction between several arylboronic acids and aryl or heteroaryl chlorides.

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Bibliographic Details
Published in:Tetrahedron letters 2005-05, Vol.46 (18), p.3205-3208
Main Authors: Konovets, Anzhelika, Penciu, Alexandra, Framery, Eric, Percina, Nathalie, Goux-Henry, Catherine, Sinou, Denis
Format: Article
Language:English
Subjects:
Carbohydrate
Catalysis
Chemical Sciences
Dicyclohexylarylphosphine
Suzuki coupling
Water soluble
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Description
Summary:[Display omitted] The synthesis of a new d-glucosamine-based dicyclohexylarylphosphine has been developed. The catalytic performance of this neutral ligand is demonstrated in the Suzuki–Miyaura cross-coupling reaction between several arylboronic acids and aryl or heteroaryl chlorides.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2005.03.049