Asymmetric Hydroesterification Of Diarylmethyl Carbinols

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION(2021)

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Abstract
An efficient asymmetric hydroesterfication of diarylmethyl carbinols is developed for the first time with a Pd-WingPhos catalyst, resulting in a series of chiral 4-aryl-3,4-dihydrocoumarins in excellent enantioselectivities and good yields. The method features mild reaction conditions, a broad substrate scope, use of easily accessible starting materials, and low palladium loadings. A plausible stereochemical model is also proposed with the Pd-WingPhos catalyst. This method has enabled a 4-step asymmetric synthesis of (R)-tolterodine from readily available starting materials.
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Key words
carbon monoxide, diarylmethyl carbinols, enantioselectivity, hydroesterification, tolterodine
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