Synthetic Route to Oscillatoxin D and Its Analogues

Org Lett. 2017 Nov 3;19(21):5992-5995. doi: 10.1021/acs.orglett.7b03032.

Abstract

O-Methyloscillatoxin D and its analogues were concisely synthesized by a bioinspired intramolecular Mukaiyama aldol reaction as a key step, which involves the construction of a novel spiro-ether moiety.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Molecular Structure
  • Spiro Compounds / chemistry*
  • Stereoisomerism

Substances

  • Spiro Compounds