-
found early in the
total synthesis of the
biologically active cardenolide ouabagenin by Phil
Baran and coworkers. The
optimized conditions minimize side reactions...
-
ester bonds in G were
hydrolyzed to
produce ouabagenin, a
precursor to ouabain. The
glycosylation of
ouabagenin with
rhamnose produced ouabain.
Poisons derived...
- (±)-garsubellin A, stigmalone, vinblastine, (±)-cortistatin A, (±)-lahadinine B,
ouabagenin, pectenotoxin-2, (±)-indoxamycin B, tri****rmatide A, (+)-omphadiol and...
