Usami Yoshihide, Numata Atsushi
Osaka University of Pharmaceutical Sciences, Takatsuki, Osaka 569-1094, Japan.
Chem Pharm Bull (Tokyo). 2004 Sep;52(9):1125-9. doi: 10.1248/cpb.52.1125.
The reactivity of two hydroxy groups in some multioxygenated cyclohexanoids was examined for basic study of the synthesis of the cytotoxic marine natural product pericosine B and related compounds. Differences in reactivity for O-methylation or O-acylation among substrates were observed.
为了对具有细胞毒性的海洋天然产物紫苏霉素B及相关化合物的合成进行基础研究,对一些多氧化环己烷类化合物中两个羟基的反应活性进行了研究。观察到底物之间在O-甲基化或O-酰化反应活性上的差异。