炔丙基
化学
反应性(心理学)
区域选择性
试剂
电泳剂
有机化学
组合化学
碘化物
卤化
炔丙醇
碘
催化作用
医学
替代医学
病理
作者
Tabassum Khan,Srinivasarao Yaragorla
标识
DOI:10.1002/ejoc.201900474
摘要
Iodocyclization of propargyl alcohols is an active area for the construction of hetero/carbocyclic iodides. Ambiphilic reactivity of propargyl alcohols made it more attractive to tune their reactivity towards the development of regioselective synthetic strategies. In general, iodocyclization reactions are atom and step economic, promoted by simple and readily available inexpensive electrophilic iodine reagents at ambient temperature. These compounds find potential applications in pharmaceutical and material sciences, because of the presence of a preinstalled reactive iodide functionality. Therefore, many researchers are actively involved in developing synthetic strategies towards iodocyclizations from propargyl alcohols for various applications. In this mini‐review, we emphasize the full list of synthetic endeavors made towards the “iodocyclization of propargyl alcohols, propargyl ethers and homopropargyl alcohols”.
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