Asymmetric aza-[3+3] annulation in the synthesis of indolizidines: an unexpected reversal of regiochemistry

Org Lett. 2011 Aug 19;13(16):4402-5. doi: 10.1021/ol2017438. Epub 2011 Jul 25.

Abstract

An enantioselective and diastereoselective aza-[3+3] annulation of pyrrolidine-based exo-cyclic vinylogous amides and urethanes with chiral vinyl iminium salts is described. This asymmetric annulation manifold is possible because of an unexpected regiochemical reversal whereby head-to-tail annulations dominated over the predicted head-to-head. It should find prevalent synthetic applications in the enantioselective synthesis of indolizidines.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aza Compounds / chemistry*
  • Indolizidines / chemical synthesis*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Aza Compounds
  • Indolizidines