Abstract
Allylic alkylation of racemic 1-arylprop-2-enyl acetates [ArCH(OAc)CHCH 2 ] with the sodium enolate of dimethyl methylmalonate in the presence of a palladium catalyst coordinated with (R)-2-diphenylphosphino-2′-methoxy-1,1′-binaphthyl [(R)-MeO-MOP] proceeds with high branch selectivity (90%) to give chiral products [ArC*H(Nu)CHCH 2 ] of up to 87% ee.
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