作者:Mahender Reddy Marri、Arun Kumar Macharla、Swamy Peraka、Narender Nama
DOI:10.1016/j.tetlet.2011.09.106
日期:2011.12
A simple, efficient, mild, and regioselective method for oxyiodination of carbonyl compounds has been reported by using NH4I as the source of iodine and Oxone® as an oxidant. Various carbonyl compounds such as aralkyl ketones, aliphatic ketones (acyclic and cyclic), and β-keto esters proceeded to the respective α-monoiodinated products in moderate to excellent yields. Unsymmetrical aliphatic ketones
通过使用NH 4 I作为碘的来源和Oxone®作为氧化剂,已经报道了一种简单,有效,温和和区域选择性的羰基化合物氧碘化方法。各种羰基化合物(如芳烷基酮,脂族酮(无环和环状)和β-酮酯)以中等至优异的收率发展为各自的α-单碘化产物。不对称脂族酮反应平稳,生成1-碘和3-碘酮的混合物,主要形成1-碘产物。