脱羧
化学
甲基化
立体化学
可扩展性
组合化学
氧化脱羧
有机化学
药物化学
重排
作者
Shi‐Hui Shi,Siqi Liu,Jian Wei,Xue Sun,Xue Li,Meng-Yao Song,Haoyang Liu
标识
DOI:10.1021/acs.orglett.6c04317
摘要
Abstract Exploiting Kolbe decarboxylation for methyl-radical transformations beyond conventional dimerization remains a longstanding synthetic challenge. Herein, we address this challenge by switching from classical Kolbe decarboxylation to iodanyl radical-mediated electrolysis, which enables decarboxylative methylation of heterocycles on sustainable graphite anodes and is scalable to gram quantities. This strategy also supports CD3-methylation of heterocycles and the late-stage methylation of biomolecules. Nearly two centuries after Kolbe decarboxylation, this organoiodine-mediated protocol overcomes its limitations, opening a route to lead compounds.
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