Dictating Thermodynamic Control through Tethering: Applications to Stereoselective Bis-Spiroketal Synthesis

Angew Chem Int Ed Engl. 2020 Apr 16;59(16):6622-6626. doi: 10.1002/anie.201916270. Epub 2020 Feb 25.

Abstract

Approaches to stereocontrol that invoke thermodynamic control fail when two or more potential products are energetically similar, but rational structural perturbations can be employed to break the energetic degeneracy and provide selective transformations. This manuscript illustrates that tethering is an effective approach for the stereoselective construction of bis-spiroketals with thermodynamically similar stereoisomers, providing a new approach to set remote stereocenters and prepare complex structures that have not previously been accessed stereoselectively.

Keywords: cyclization; diastereoselectivity; macrocycles; oxygen heterocycles; spiro compounds.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biological Products / chemical synthesis
  • Biological Products / chemistry
  • Catalysis
  • Coordination Complexes / chemistry
  • Cyclization
  • Furans / chemical synthesis*
  • Furans / chemistry
  • Rhenium / chemistry
  • Spiro Compounds / chemical synthesis*
  • Spiro Compounds / chemistry
  • Stereoisomerism
  • Thermodynamics

Substances

  • Biological Products
  • Coordination Complexes
  • Furans
  • Spiro Compounds
  • spiroketal
  • Rhenium