Synthesis of C-19-functionalized 1alpha-hydroxyvitamin D(2) analogues via ring-closing metathesis

Org Lett. 2003 Mar 6;5(5):669-72. doi: 10.1021/ol027406w.

Abstract

A heteroatom-tethered regioselective ring-closing metathesis reaction was used for the C-19 functionalization of 1alpha-hydroxy-5,6-trans-vitamin D(2) analogues. Applications of the reaction to form a range of analogues by manipulation of the tether using both organolithium reagents and Diels-Alder cycloadditions are described.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Ergocalciferols / chemical synthesis
  • Ergocalciferols / chemistry*
  • Indicators and Reagents
  • Metalloporphyrins / chemistry
  • Stereoisomerism
  • Zinc

Substances

  • Ergocalciferols
  • Indicators and Reagents
  • Metalloporphyrins
  • 1 alpha-hydroxyergocalciferol
  • Zinc