4.5 Article

Convenient synthesis of difluoromethyl alcohols from both enolizable and non-enolizable carbonyl compounds with difluoromethyl phenyl sulfone

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2005, 期 11, 页码 2218-2223

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200500101

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difluoromethyl phenyl sulfone; nucleophilic reaction; difluoromethylation; fluorine; reductive desulfonylation

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A general and efficient nucleophilic difluoromethylation of carbonyl compounds (both enolizable and non-enolizable aldehydes and ketones) has been achieved by using a nucleophilic (phenylsulfonyl)difluoromethylation-reductive desul-fonylation strategy. Difluoromethyl phenyl sulfone acts as a difluoromethyl anion (CF2H-) equivalent. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005).

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