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Scope of the Suzuki-Miyaura cross-coupling reaction of potassium trifluoroboratoketohomoenolates.

ABSTRACT: Potassium trifluoroboratoketohomoenolates were prepared in good yields from either the corresponding alpha,beta-unsaturated compounds or methyl ketones. These organoboron reagents were effectively cross-coupled with various aryl and heteroaryl chlorides.

SUBMITTER: Molander GA

PROVIDER: S-EPMC2676431 | biostudies-literature | 2009 Feb

REPOSITORIES: biostudies-literature

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Scope of the Suzuki-Miyaura cross-coupling reaction of potassium trifluoroboratoketohomoenolates.

Molander Gary A GA Jean-Gérard Ludivine L

The Journal of organic chemistry 20090201 3

Potassium trifluoroboratoketohomoenolates were prepared in good yields from either the corresponding alpha,beta-unsaturated compounds or methyl ketones. These organoboron reagents were effectively cross-coupled with various aryl and heteroaryl chlorides. ...[more]

PMID: 19133770

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