作者:Stephen J. Angyal、Léon Odier
DOI:10.1016/s0008-6215(00)81001-0
日期:1982.3
inositols by blocking all but one hydroxyl group, converting the free hydroxyl group into its S -methyl dithiocarbonate, and treating it with tributylstannane. Suitable blocking-groups are methyl, benzyl, and methylthiomethyl ethers, and acetals. One cyclohexanepentol was prepared by the reductive deamination of an aminodeoxyinositol.
摘要从肌醇中合成了几种环己烷戊醇,方法是封闭除一个羟基外的所有羟基,将游离羟基转化为S-甲基二硫代碳酸酯,并用三丁基锡烷处理。合适的保护基是甲基,苄基和甲硫基甲基醚和乙缩醛。一种环己烷戊醇是通过氨基脱氧肌醇的还原性脱氨基反应制得的。