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Conformational analysis and intramolecular interactions in monosubstituted phenylboranes and phenylboronic acids

  • Josué M. Silla,
  • Rodrigo A. Cormanich,
  • Roberto Rittner and
  • Matheus P. Freitas

Beilstein J. Org. Chem. 2013, 9, 1127–1134, doi:10.3762/bjoc.9.125

Graphical Abstract
  • corresponding conformers appreciably populated, because of steric effects and the loss of πCC→pB resonance. Thus, the results found earlier for 2-fluorophenol about the lack of intramolecular hydrogen bonding are now corroborated. Keywords: conformational analysis; hydrogen bond; interactions with boron
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Published 11 Jun 2013
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