化学
脱羧
电化学
级联
组合化学
立体选择性
金属
电解质
分子
转化(遗传学)
立体化学
脱质子化
立体异构
计算化学
动能
级联反应
同位素标记
产量(工程)
形式综合
氧化脱羧
光化学
支撑电解质
反应机理
作者
Sébastien Meyer,Aurélie Claraz
出处
期刊:Organic Letters
[American Chemical Society]
日期:2025-12-05
卷期号:27 (50): 13756-13761
被引量:1
标识
DOI:10.1021/acs.orglett.5c04198
摘要
Electrochemistry offers new opportunities for radical Truce-Smiles rearrangement (TSR). Herein, we disclose an electrochemical decarboxylation of redox-active esters that triggers a nondesulfonylative TSR of N-arylsulfonylpropiolamides, delivering 4-aryl-5-alkyl isothiazolidinone dioxides. We uncovered a subtle interplay between anodically generated metallic salts and the selected electrolyte anion, favoring either kinetic or thermodynamic isomers with moderate and high diastereoselectivities, respectively. Further transformation smoothly provides the formal desulfonylative TSR adduct, expanding the synthetic utility of the method.
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