酰胺
试剂
化学
酰化
组合化学
六氟磷酸盐
反应性(心理学)
肽键
功能群
有机合成
有机化学
基质(水族馆)
工具箱
化学选择性
高分子化学
密度泛函理论
群(周期表)
离子液体
保护组
氢键
固相合成
作者
Gregory L. Beutner,Ian S. Young
标识
DOI:10.1021/acs.oprd.6c00060
摘要
N, N, N′, N ′ -Tetramethylchloroformamidinium hexafluorophosphate and N -methylimidazole (TCFH-NMI), a reagent combination for acylation reactions first described in 2018, is gaining recognition and finding applications from research laboratories through to large-scale manufacturing. In this review, we will detail the unique properties of this method for amide bond formation before discussing its extension into the synthesis of esters, ketones, and other functional group transformations. The high reactivity of the N -acyl imidazolium ion, the unique activated ester intermediate accessible by this method, provides for a broad substrate scope under mild conditions. In combination with the favorable safety characteristics of these reagents and ease of isolation provided by the simple water-soluble byproducts, TCFH-NMI should prove an impactful addition to the organic chemists’ toolbox alongside more commonly used amide bond-forming reagents.
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