Beilstein Journal of Organic Chemistry (Oct 2013)

Regioselective carbon–carbon bond formation of 5,5,5-trifluoro-1-phenylpent-3-en-1-yne

  • Motoki Naka,
  • Tomoko Kawasaki-Takasuka,
  • Takashi Yamazaki

DOI
https://doi.org/10.3762/bjoc.9.256
Journal volume & issue
Vol. 9, no. 1
pp. 2182 – 2188

Abstract

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The regioselective carbon–carbon bond formation was studied using 5,5,5-trifluoro-1-phenylpent-3-en-1-yne as a model substrate, and predominant acceptance of electrophiles β to a CF3 group as well as a deuterium trap experiment of the lithiated species led to the conclusion that the obtained regioselectivity is kinetically determined for the reactions with electrophiles, under equilibration of the possible two anionic species.

Keywords