Enhancement of enantioselectivity by THF in asymmetric mo-catalyzed olefin metathesis. Catalytic enantioselective synthesis of cyclic tertiary ethers and spirocycles

J Am Chem Soc. 2002 Sep 11;124(36):10779-84. doi: 10.1021/ja020671s.

Abstract

Mo-catalyzed enantioselective rearrangement of achiral cyclopentenyl tertiary ethers to chiral cyclohexenyl tertiary ethers are reported. These olefin metathesis transformations proceed efficiently and with high levels of enantioselectivity. A noteworthy feature of these reactions is that added tetrahydrofuran exerts a remarkably positive influence on the enantioselectivity of the metathesis-based rearrangement. The first examples of catalytic asymmetric synthesis of spirocyclic structures by enantioselective olefin metathesis are also disclosed.

Publication types

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

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Ethers, Cyclic / chemical synthesis*
  • Furans / chemistry*
  • Molybdenum / chemistry*
  • Organometallic Compounds / chemistry
  • Solvents
  • Spiro Compounds / chemical synthesis*
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Alkenes
  • Ethers, Cyclic
  • Furans
  • Organometallic Compounds
  • Solvents
  • Spiro Compounds
  • tetrahydrofuran
  • Molybdenum