337367-48-3Relevant academic research and scientific papers
Low temperature domino reactions. A ready access to trifluoromethyl substituted butenolides and their thioanalogues
Burger, Klaus,Fuchs, Annett,Hennig, Lothar,Helmreich, Brigitte
, p. 1657 - 1659 (2001)
Domino reactions are described, including nucleophilic substitution, Claisen rearrangement and Cope rearrangement, which provide ready access to trifluoromethyl substituted butenolides and their thioanalogues, starting from 2-fluoro-3-trifluoromethyl furans and thiophenes, respectively.
Domino reactions with fluorinated five-membered heterocycles - Syntheses of trifluoromethyl substituted butenolides and γ-ketoacids
Burger, Klaus,Hennig, Lothar,Fuchs, Annett,Greif, Dieter,Spengler, Jan,Albericio, Fernando
, p. 1763 - 1779 (2007/10/03)
A new approach to trifluoromethyl substituted butenolides and their thioanalogues is described starting from 2-fluoro-3-trifluoromethylfurans and -thiophenes, respectively. The reaction sequence includes three steps - nucleophilic displacement reaction, Claisen, and finally Cope rearrangement - which can be run as domino reaction. A modification of the domino reaction (transesterification instead of Cope rearrangement) provides a concise access to α-trifluoromethyl-γ-ketoacids. Springer-Verlag 2005.
