Indole diterpenoid synthetic studies. Construction of the heptacyclic core of (-)-nodulisporic acid D

Org Lett. 2006 Apr 13;8(8):1669-72. doi: 10.1021/ol0602912.

Abstract

[structure: see text] Construction of the heptacyclic core of (-)-nodulisporic acid D, a representative member of a recently discovered class of architecturally complex, ectoparasiticidal indole alkaloids, has been achieved. The modular synthetic strategy comprises an expedient, stereocontrolled synthesis of a tricyclic western hemisphere, in conjunction with union of an eastern hemisphere, exploiting the 2-substituted indole synthetic protocol introduced and developed in our laboratory.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diterpenes / chemical synthesis*
  • Diterpenes / chemistry
  • Indoles / chemical synthesis*
  • Indoles / chemistry*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Diterpenes
  • Indoles
  • nodulisporic acid D