Ultimate convergence for the total synthesis of calicheamicin γ has been achieved thanks to a remarkable glycosidation between the glycosyl donor 2 and aglycone ent-1 (see preceeding communication; R = SSMe, ketal-protected); after glycosidation the natural product is obtained in two steps.
No takes yet. Share an insight, caveat, or question.
Hitchcock et al. (1994) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: