Toward the total synthesis of carthamin, a stereoselective approach to the C-glycosyl quinochalcone intermediate is reported via the desymmetrization of a pseudo-Cs-symmetric C-glycosyl cyclohexadienone. Click to show full abstract
Toward the total synthesis of carthamin, a stereoselective approach to the C-glycosyl quinochalcone intermediate is reported via the desymmetrization of a pseudo-Cs-symmetric C-glycosyl cyclohexadienone.
               
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