化学选择性
化学
反应性(心理学)
多样性(控制论)
纳米技术
生化工程
组合化学
有机化学
计算机科学
催化作用
人工智能
工程类
替代医学
材料科学
医学
病理
作者
Jigyansa Sahoo,Jeetendra Panda,Sukanya Mandal,Gokarneswar Sahoo
标识
DOI:10.1002/ejoc.202400160
摘要
The most challenging aspect of chemical synthesis has always been attainment of high chemoselectivity levels. This review will provide a panoramic view on how the innate reactivity of two nearly reactive functional groups (‐O/‐N) can be controlled or reversed for the chemoselective functionalisation in alkanolamines. A comprehensive compilation of reports encasing various methodologies developed to accomplish selective O/N functionalisation in amino alcohols has been documented. In this review, we go over a number of findings that have been studied in recent decades using a variety of synthetic approaches. To help us organize and emphasize the important ideas that have been emerging as a result of these research, we have concentrated on the suggested mechanistic basis of the reactions that are being surveyed.
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