Journal article

Total synthesis of the proposed structure for spirofungin B: A reassignment of the stereochemistry

SD Zanatta, JM White, MA Rizzacasa

Organic Letters | AMER CHEMICAL SOC | Published : 2004

Abstract

(Equation presented) The total synthesis of the proposed structure for spirofungin B (2) is described. The data for the synthetic material did not compare with that for the natural product leading to the conclusion that the structure 2 assigned for spirofungin B is incorrect. Analysis of the NMR data reported for spirofungins A and B as well as related spiroketals allowed for the reassignment of the stereochemistry of spirofungin B to be that corresponding to 15-epi-spirofungin A (27).

University of Melbourne Researchers