First enantioselective synthesis of tetracyclic intermediates en route to madangamine D

Chem Commun (Camb). 2013 Apr 18;49(30):3149-51. doi: 10.1039/c3cc41104d. Epub 2013 Mar 11.

Abstract

The enantioselective synthesis of advanced tetracyclic precursors of madangamine D, bearing rings ABCD of this alkaloid, is reported. The saturated 14-membered ring is assembled from functionalized diazatricyclic intermediates following either ring-closing metathesis or macrolactamization strategies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Heterocyclic Compounds, 4 or More Rings / chemical synthesis
  • Heterocyclic Compounds, 4 or More Rings / chemistry*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Heterocyclic Compounds, 4 or More Rings
  • madangamine D