From 2-aminomethyl-1,4-benzodioxane enantiomers to unichiral 2-cyano- and 2-carbonyl-substituted benzodioxanes via dichloroamine

J Org Chem. 2014 Jul 18;79(14):6732-7. doi: 10.1021/jo500964y. Epub 2014 Jun 26.

Abstract

2-Substituted 1,4-benzodioxanes, such as 2-cyano-, 2-methoxycarbonyl-, 2-aminocarbonyl-, and 2-formyl-1,4-benzodioxane, are key synthons that for the most part are never described as enantiomers or are inadequately characterized for enantiomeric purity. They were prepared by quantitative N,N-dichlorination of (R)- and (S)-2-aminomethyl-1,4-benzodioxane and successive functional group conversions in high yields without any racemization of the stereogenic benzodioxane C(2).

MeSH terms

  • Chloramines / chemistry*
  • Dioxanes / chemical synthesis*
  • Dioxanes / chemistry
  • Methylamines / chemistry*
  • Molecular Structure
  • Stereoisomerism

Substances

  • 2-aminomethyl-1,4-benzodioxane
  • Chloramines
  • Dioxanes
  • Methylamines