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Use of potassium beta-trifluoroborato amides in Suzuki-Miyaura cross-coupling reactions.

ABSTRACT: Potassium beta-trifluoroborato amides were prepared and used as successful partners in Suzuki-Miyaura reactions with various aryl chlorides, including electron-rich and electron-poor derivatives, as well as several heteroaryl chloride partners.

SUBMITTER: Molander GA

PROVIDER: S-EPMC2736348 | biostudies-literature | 2009 Aug

REPOSITORIES: biostudies-literature

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Use of potassium beta-trifluoroborato amides in Suzuki-Miyaura cross-coupling reactions.

Molander Gary A GA Jean-Gérard Ludivine L

The Journal of organic chemistry 20090801 15

Potassium beta-trifluoroborato amides were prepared and used as successful partners in Suzuki-Miyaura reactions with various aryl chlorides, including electron-rich and electron-poor derivatives, as well as several heteroaryl chloride partners. ...[more]

PMID: 19572522

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