Abstract
The new ferrocene-based P,S-chiral auxiliary 1, derived from thioglucose, has been prepared and used in the palladium-catalyzed enantioselective allylic alkylation reaction. The X-ray structure of the allyl cationic complex [Pd(η3-PhCHCHCHPh)(1)]CF3SO3 (2) reveals a markedly rotated 1,3-diphenylallyl ligand such that the terminal allyl carbon C(3), trans to the phosphorus donor, is ca. 0.85(3) A below the coordination plane. This distortion is pertinent to the Pd(0) transition state complex expected in the allylic alkylation reaction.
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