626242-99-7Relevant articles and documents
Total Synthesis and Conformational Analysis of the Antifungal Agent (-)-PF1163B
Bouazza, Fodil,Renoux, Brigitte,Bachmann, Christian,Gesson, Jean-Pierre
, p. 4049 - 4052 (2003)
(Equation presented) (-)-PF1163B, a new macrocyclic antifungal antibiotic isolated from Streptomyces sp., has been prepared in eight steps from (S)-citronellene. The key step is a ring-closing metathesis reaction of an ester and amide derivative obtained from a substituted N-methyl-L-tyrosine.
Total synthesis of the antifungal antibiotic PF1163A
Krishna, Palakodety Radha,Srinivas, Palabindela
, p. 769 - 774 (2012/09/05)
The total synthesis of a novel antifungal antibiotic PF1163A is reported utilising Keck asymmetric allylation, Sharpless kinetic resolution, regioselective epoxide-ring opening, esterification and ring-closing metathesis as the key reactions.