Synthesis and functionalization of 3-alkylidene-1,2-diazetidines using transition metal catalysis

Org Lett. 2011 Apr 1;13(7):1686-9. doi: 10.1021/ol200193n. Epub 2011 Mar 2.

Abstract

An efficient two-step synthesis of a wide range of 3-methylene-1,2-diazetidines has been developed through application of a Cu(I)-catalyzed 4-exo ring closure. The double bond of this new class of strained heterocycle can be functionalized in a stereocontrolled manner by using palladium-catalyzed Heck reactions. Moreover, chemoselective reduction of 3-alkylidene-1,2-diazetidines gives access to saturated 1,2-diazetidines and vicinal diamines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Azetidines / chemical synthesis*
  • Azetidines / chemistry
  • Catalysis
  • Copper / chemistry*
  • Molecular Structure
  • Oxidation-Reduction
  • Palladium / chemistry*
  • Stereoisomerism

Substances

  • Azetidines
  • azetidine
  • Palladium
  • Copper