ol016365l_si_001.pdf (94.93 kB)
Total Synthesis of (−)-Callystatin A
journal contribution
posted on 2001-09-07, 00:00 authored by Markus Kalesse, Monika Quitschalle, Chary P. Khandavalli, Aamer SaeedThe enantioselective synthesis of callystatin A is described. The pivotal step in the synthesis is the stereoselective aldol reaction that generates
the β-hydroxy ketone moiety. Utilizing the allylic strain within the ethyl ketone precursor, we were able to generate the all-syn configuration
of callystatin A. For the construction of the two diene moieties, both a Heck coupling and a Wittig reaction were employed.