Chemistry Letters p. 677 - 678 (1995)
Update date:2022-08-05
Topics:
Matsumoto, Takashi
Sohma, Tsukasa
Yamaguchi, Hiroki
Suzuki, Keisuke
An efficient two-step access to C-glycosyl juglones promising synthetic intermediates toward aryl C-glycoside antibiotics, has been developed based on (1) the O->C-glycoside rearrangement and (2) the regioselective cycloaddition of α-alkoxybenzyne and α-oxyfuran.
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