Abstract
AbstractThe cross coupling reaction of aryl and vinyl boronic acids and allylic alcohols proceeded smoothly in toluene or dioxane in the presence of a (triphenyl phosphite)palladium catalyst to give the corresponding allylbenzene derivatives and 1,4‐dienes. Neither cocatalysts for promoting C−O bond cleavage of allylic alcohols nor bases for activation of organoboron reagents are required for promoting the coupling process. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)
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