Self-assembling bisurea macrocycles used as an organic zeolite for a highly stereoselective photodimerization of 2-cyclohexenone

J Am Chem Soc. 2006 Jun 28;128(25):8122-3. doi: 10.1021/ja062337s.

Abstract

We report a highly selective 2 + 2 cycloaddition of 2-cyclohexenone in the presence of self-assembled bisurea macrocycles that yields the head-to-tail photodimer. The reaction proceeds with high conversion and with decreased incidence of secondary photorearrangement. Furthermore, the product can be extracted from the assembly, and the solid assembly is readily recovered and reused, much like a zeolite.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Chemistry, Organic
  • Cyclohexanones / chemistry*
  • Dimerization
  • Macrocyclic Compounds / chemical synthesis*
  • Macrocyclic Compounds / chemistry
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Organic Chemistry Phenomena
  • Photochemistry
  • Porosity
  • Stereoisomerism
  • Urea / chemistry*
  • Zeolites / chemistry*

Substances

  • Cyclohexanones
  • Macrocyclic Compounds
  • Zeolites
  • 2-cyclohexen-1-one
  • Urea