Synthesis of 4-membered carbasugars by way of stereoselective SmI2-mediated aldehyde-alkene cyclization

J Org Chem. 2013 Jul 5;78(13):6751-7. doi: 10.1021/jo400732a. Epub 2013 Jun 21.

Abstract

A stereodivergent synthesis of the first examples of 4-membered carbasugars has been achieved from vitamin C by way of an efficient intramolecular SmI2-mediated aldehyde-alkene coupling. In this key step, cylobutanes with four contiguous asymmetric centers are generated with a high level of stereocontrol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry*
  • Alkenes / chemistry*
  • Carbasugars / chemical synthesis*
  • Carbasugars / chemistry
  • Cyclization
  • Molecular Conformation
  • Stereoisomerism

Substances

  • Aldehydes
  • Alkenes
  • Carbasugars