📜(2S,3S,4S,5R,6R)-6-[[(3S,4Ar,6Ar,6Bs,8As,12As,14Ar,14Br)-4,4,6A,6B,11,11,14B-Heptamethyl-8A-[(2S,3R,4S,5R,6R)-3,4,5-Tribenzoyloxy-6-(Benzoyloxymethyl)Oxan-2-Yl]Oxycarbonyl-1,2,3,4A,5,6,7,8,9,10,12,12A,14,14A-Tetradecahydropicen-3-Yl]Oxy]-4-Benzoyloxy-3-Hydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-Tribenzoyloxy-6-(Benzoyloxymethyl)Oxan-2-Yl]Oxyoxane-2-Carboxylic Acid置于sodium Methylate体系中,用 甲醇,二氯甲烷 作为反应溶剂,以72%的收率获得产物人参皂苷ro
参考文献:Facile Synthesis Of Ginsenoside Ro
标题:Facile Synthesis Of Ginsenoside Ro
摘要:我们开发了两条简明的合成路线,它们在糖基化顺序上有所不同,最终都导向人参皂苷 Ro (1).这些合成路线的特点是,在后期通过 Tempo 介导的选择性氧化来处理葡萄糖醛酸残基,并引入 Azmb 作为邻苯甲酰基参与基团,以便日后选择性去除.
DOI:10.1055/s-2003-44985