Formation of pinacol boronate esters via pyridine iodoborane hydroboration

J Org Chem. 2008 Dec 5;73(23):9508-10. doi: 10.1021/jo8020049.

Abstract

Hydroboration of alkenes with pyridine iodoborane followed by treatment with pinacol/NaOH affords monoalkyl pinacol boronates in moderate to good yield. Dialkylborinic acid derivatives are formed competitively, especially in the case of terminal alkenes. This side reaction can be minimized by using excess of pyridine iodoborane. More hindered alkenes give the best results.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkenes
  • Boranes / chemistry*
  • Boronic Acids / chemistry*
  • Chemistry, Organic / methods*
  • Esters
  • Iodine Compounds / chemistry*
  • Ions
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Pyridines / chemistry*
  • Temperature

Substances

  • Alkenes
  • Boranes
  • Boronic Acids
  • Esters
  • Iodine Compounds
  • Ions
  • Pyridines