The Journal of Organic Chemistry

Scope and limitations of the palladium-catalyzed cross-coupling reaction of in situ generated organoboranes with aryl and vinyl halides

SP Maddaford, BA Keay

Index: Maddaford, Shawn P.; Keay, Brian A. Journal of Organic Chemistry, 1994 , vol. 59, # 22 p. 6501 - 6503

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Citation Number: 72

Abstract

Summary: The in situ palladium (0)-catalyzed Suzuki reaction is shown to be an efficient method for the crosscoupling of aryl-, furyl-, primary, and benzylic boranes with aryl or vinyl bromides and iodides without the isolation of the organoboronic acid or the addition of any external base.

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