芳基
化学
亲核细胞
周环反应
试剂
反应性(心理学)
计算化学
反应中间体
组合化学
呋喃
俘获
有机化学
催化作用
病理
生物
医学
替代医学
生态学
作者
Theresa M. McCormick,David R. Stuart,Bryan E. Metze,Avik Bhattacharjee
出处
期刊:Synthesis
[Thieme Medical Publishers (Germany)]
日期:2022-05-06
卷期号:54 (22): 4989-4996
被引量:7
摘要
Abstract Arynes are highly reactive intermediates that may be used strategically in synthesis by trapping with arynophilic reagents. However, ‘arynophilicity’ of such reagents is almost completely anecdotal and predicting which ones will be efficient traps is often challenging. Here, we describe a systematic study to parameterize the arynophilicity of a wide range of reagents known to trap arynes. A relative reactivity scale, based on one-pot competition experiments, is presented by using furan as a reference arynophile and 3-chlorobenzyne as a the aryne. More than 15 arynophiles that react in pericyclic reactions, nucleophilic addition, and σ-bond insertion reactions are parameterized with arynophilicity (A) values, and multiple aryne precursors are applicable.
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