Regioselective functionalization of 2-arylazetidines: evaluating the ortho-directing ability of the azetidinyl ring and the α-directing ability of the N-substituent

Chem Commun (Camb). 2014 Feb 18;50(14):1698-700. doi: 10.1039/c3cc48555b. Epub 2014 Jan 6.

Abstract

The regioselective lithiation-functionalization of 2-arylazetidines has been explored. The nature of the N-substituent is mainly responsible for a regioselectivity switch. ortho-Lithiation occurred, using hexyllithium as a greener base, in N-alkylazetidines, while α-benzylic lithiation has been observed with N-Boc azetidines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azetidines / chemistry*
  • Magnetic Resonance Spectroscopy
  • Nitrogen / chemistry*
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Azetidines
  • Nitrogen