Copper-Catalyzed Di- and Trifluoromethylation of α,β-Unsaturated Carboxylic Acids: A Protocol for Vinylic Fluoroalkylations

Dual action: The Lewis acid CuF2⋅2 H2O efficiently catalyzes the reaction between electrophilic fluoroalkylating agents and α,β‐unsaturated carboxylic acids by dually activating both reactants, thus affording di‐ and trifluoromethyl alkenes in high yields with excellent E/Z selectivity.

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Veröffentlicht in:Angewandte Chemie International Edition 2012-04, Vol.51 (16), p.3944-3947
Hauptverfasser: He, Zhengbiao, Luo, Tao, Hu, Mingyou, Cao, Yanjing, Hu, Jinbo
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container_title Angewandte Chemie International Edition
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creator He, Zhengbiao
Luo, Tao
Hu, Mingyou
Cao, Yanjing
Hu, Jinbo
description Dual action: The Lewis acid CuF2⋅2 H2O efficiently catalyzes the reaction between electrophilic fluoroalkylating agents and α,β‐unsaturated carboxylic acids by dually activating both reactants, thus affording di‐ and trifluoromethyl alkenes in high yields with excellent E/Z selectivity.
doi_str_mv 10.1002/anie.201200140
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Alkenes
Alkylation
carboxylic acids
Carboxylic Acids - chemistry
Catalysis
copper
Copper - chemistry
fluorine
Fluorine - chemistry
stereoselectivity
synthetic methods
Vinyl Compounds - chemistry
title Copper-Catalyzed Di- and Trifluoromethylation of α,β-Unsaturated Carboxylic Acids: A Protocol for Vinylic Fluoroalkylations
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