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January 1, 2000Synthesis113 citations

Diastereoselective Allylation and Crotylation Reactions of Aldehydes with Potassium Allyl- and Crotyltrifluoroborates under Lewis Acid Catalysis

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RBRobert A. BateyATAvinash N. ThadaniDSDavid Smil

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Abstract

All articles of this category Potassium allyl- and crotyltrifluoroborates react with aldehydes in a process catalyzed by a variety of Lewis acids, to give the corresponding homoallylic alcohols. Of the Lewis acids examined, BF 3 · OEt 2 , used either stoichiometrically or catalytically, was found to most efficiently catalyze this reaction. The air and moisture stable potassium organotrifluoroborate salts react with a variety of alkyl, α- or β-substituted alkyl, and aryl aldehydes, and lead to the adducts in high yield and with high diastereoselectivity. allylations - boron - alcohols - Lewis acids - catalysis

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Cite This Study

Batey et al. (2000) studied this question.

synapsesocial.com/papers/6a9913de0b64aa5b17f0cd35https://doi.org/10.1055/s-2000-6303
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