Nodulisporic acid side-chain modifications: access to the 2", 3", 4", and 6" registers

Bioorg Med Chem Lett. 2003 Jan 6;13(1):147-50. doi: 10.1016/s0960-894x(02)00826-0.

Abstract

Efficient routes to access the 2", 3", 4", and 6" registers of the nodulisporic acid (NsA) side chain are disclosed. A mild one-carbon, Ph(2)CdoublebondNCH(2)CtriplebondN mediated homologation of NsA's 3"-aldehyde permitted access to the 4"-register. Curtius reaction of NsA's 3"-acid yielded the corresponding 2"-aldehyde 4 from which the unnatural Delta(2",3")-olefin isomer 2b was obtained. In addition, Arndt-Eistert reactions of the parent NsA permitted a one-carbon homologation to the 6" register. These efforts identified new analogues with significant flea activity and illustrated the biological significance of unsaturation at the 1",2" register.

MeSH terms

  • Alkenes
  • Animals
  • Dose-Response Relationship, Drug
  • Indoles / chemistry*
  • Indoles / pharmacology
  • Insecticides / chemical synthesis*
  • Insecticides / pharmacology
  • Siphonaptera / drug effects
  • Structure-Activity Relationship

Substances

  • Alkenes
  • Indoles
  • Insecticides
  • nodulisporic acid A