Biomimetic cationic polyannulation reaction catalyzed by Bi(OTf)3: cyclization of 1,6-dienes, 1,6,10-trienes, and aryl polyenes

Org Lett. 2011 Jul 1;13(13):3320-3. doi: 10.1021/ol201028f. Epub 2011 Jun 1.

Abstract

Nonactivated trienes and aryltrienes were cyclized into polycyclic compounds in good to excellent yields under bismuth triflate catalysis in a biomimetic fashion. The reaction showed broad applicability and allowed for the formation of functionalized bicyclic to tetracyclic structures from simple precursors in one pot. For some specific substrates, the cyclization was followed by a methyl shift as encountered in terpenoid biosynthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomimetic Materials / chemistry*
  • Catalysis
  • Cations / chemistry
  • Cyclization
  • Mesylates / chemistry*
  • Molecular Structure
  • Polycyclic Compounds / chemistry*
  • Polyenes / chemistry*

Substances

  • Cations
  • Mesylates
  • Polycyclic Compounds
  • Polyenes
  • Bi(OTf)3