Efficient one step procedure for the synthesis of α- trifluoromethylated arylacetates

Article abstract of DOI:10.1080/00397919808007172

The reaction of β,β-difluoro-α-trifluoromethylstyrene derivatives 1 with 3 equiv. of sodium methoxide in acetonitrile at 25°C afforded a- trifluoromethylated arylacetates 3 in good yields.

Full text of DOI:10.1080/00397919808007172

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
Efficient One Step Procedure for the Synthesis of
α-Trifluoromethylated Arylacetates
In Howa Jeong , Tae Won Park & Bum Tae Kim
To cite this article: In Howa Jeong , Tae Won Park & Bum Tae Kim (1998) Efficient One Step
Procedure for the Synthesis of α-Trifluoromethylated Arylacetates, Synthetic Communications,
28:11, 1981-1987, DOI: 10.1080/00397919808007172
To link to this article: http://dx.doi.org/10.1080/00397919808007172
Published online: 20 Aug 2006.
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Date: 12 June 2016, At: 20:12