作者:Md. Abul Hashem、Alexander Jung、Monika Ries、Andreas Kirschning
DOI:10.1055/s-1998-1596
日期:1998.2
A new and mild method for the bromoacetoxylation of olefins is presented, which is initiated by iodine(III). α-Acetoxy bromides 6-11 are generated from olefins 5 in the presence of tetraethylammonium bromide (1) and (diacetoxyiodo)benzene (2). The 1,2-addition to carbohydrate-derived enol ethers results in 2-deoxy-2-bromo-pyranosyl acetates which are versatile glycosyl donors for the synthesis of 2'-deoxy-2'-bromo glycosides 16.
提出了一种新的温和方法,用于烯烃的
溴乙酸酯化反应,该反应由
碘(III)启动。在
四乙基溴化铵(1)和(二
乙酸氧
碘)苯(2)的存在下,从烯烃5生成α-乙氧基
溴化物6-11。对
碳水化合物衍生的烯醇醚进行1,2-加成,得到2-脱氧-2-
溴-
吡喃糖
乙酸酯,这些化合物是合成2'-脱氧-2'-
溴糖苷16的多功能糖苷供体。