Starting from epothilone A-D (1a-2b) obtained by large scale fermentation o
f the myxobacterium Sorangium cellulosum the thiazole side-chain was extens
ively modified by substitution, oxidation and replacement. Metallation affo
rded the C-19 carbanion 4 which was quenched by Various carbon and heteroat
om electrophiles to give C-19 substituted epothilones 5. Thiazole N-oxides
9 were obtained by treatment of 2a and 2b with m-chloroperbenzoic acid and
rearranged by acetic anhydride to 21-acetoxy epothilones 10. Cleavage of ep
othilones A and B with ozone gave methyl ketones 11 from which carbonyl der
ivatives 12, 13, 14, and aldol condensation products 16 were prepared. Simi
larly vinyl boronic acid 17 was obtained and transformed by Suzuki coupling
or iodination/Stille coupling to aryl and heteroaryl analogs 15.