Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Chem Commun (Camb). 2013 Apr 14;49(29):2989-91. doi: 10.1039/c3cc40757h.

Abstract

Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H)-furanones resulted in rigid products (53-75%) with three spatially defined positions for further functionalisation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry
  • Azabicyclo Compounds / chemistry
  • Cycloaddition Reaction
  • Furans / chemistry
  • Heptanes / chemistry
  • Photochemical Processes
  • Pyrrolidines / chemistry*
  • Stereoisomerism

Substances

  • Amines
  • Azabicyclo Compounds
  • Furans
  • Heptanes
  • Pyrrolidines