4.8 Article

Ruthenium-catalyzed arylation of 2-alkenylpyridines with aryl bromides:: Alternative E,Z-selectivity to Mizoroki-Heck reaction

Journal

ORGANIC LETTERS
Volume 7, Issue 18, Pages 4009-4011

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol051654l

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[Graphics] Regio- and stereoselective arylation of 2-alkenylpyridines with aryl bromides is catalyzed by specific Ru(II)-phosphine complexes affording beta-arylated (Z)-2-alkenylpyridines, in which the aryl moiety is introduced cis to the pyridyl group. This geometrical selectivity is in sharp contrast to the Mizoroki-Heck reaction.

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