C-Glycosylanthraquinone synthesis: total synthesis of vineomycinone B2 methyl ester
作者:Marcus A. Tius、Jorge Gomez-Galeno、Xue Qin Gu、Javid H. Zaidi
DOI:10.1021/ja00015a035
日期:1991.7
A synthesis of substituted anthraquinones has been developed. Commercially available anthrarufin and 1,8-dihydroxyanthraquinone were converted to the corresponding (methoxymethoxy)anthracenes. Directed metalation followed by stannylation produced stable intermediates that were either alkylated, arylated, acylated, and/or C-glycosylated. The value of this new methodology was demonstrated by the triply convergent total synthesis of vineomycinone B2 methyl ester, a representative C-glycosylanthraquinone antibiotic.
TIUS, MARCUS A.;GU, XUE-QIN;GOMEZ-GALENO, JORGE, J. AMER. CHEM. SOC., 112,(1990) N2, C. 8188-8189
作者:TIUS, MARCUS A.、GU, XUE-QIN、GOMEZ-GALENO, JORGE