Johnson-Claisen rearrangement of γ-fluoro-γ-(di- or tri-fluoromethyl)allyl alcohols affording stereoselective access to β-fluoro-β-di- or tri-fluoromethylated γ, δ-unsaturated carboxylic acid esters

Journal of Fluorine Chemistry

Volumn 122, Issue 2, 2003, Pages 237-242

  Funabiki, Kazumasa ^a   Hara, Naoki ^a   Nagamori, Masashi ^a   Shibata, Katsuyoshi ^a   Matsui, Masaki ^a  

^a GIFU UNIVERSITY   (Japan)

Author keywords

Allyl alcohol; Difluoromethyl; Johnson Claisen rearrangement; Trifluoromethyl

Indexed keywords

ACETIC ACID; ALLYL ALCOHOL; CARBOXYLIC ACID DERIVATIVE; ESTER DERIVATIVE; HYDROQUINONE; ORGANOFLUORINE DERIVATIVE; PROPIONIC ACID;

ARTICLE; CATALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; METHYLATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOCHEMISTRY; TEMPERATURE; TIME;

EID: 0041802873     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-1139(03)00108-8     Document Type: Article

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