| Literature DB >> 22804460 |
Tony S N Zhao1, Kálmán J Szabó.
Abstract
A copper-mediated trifluoromethylation of propargylic halides and trifluoroacetates was performed with high allenyl or propargyl selectivity. The reaction proceeds smoothly with aliphatic and aromatic substituents bearing either electron-withdrawing or -supplying groups. Preliminary mechanistic results indicate an ionic mechanism involving nucleophilic transfer of the CF(3) group from the Cu complex to the propargylic substrate.Entities:
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Year: 2012 PMID: 22804460 DOI: 10.1021/ol3017287
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005