胺化
化学
分子间力
烯丙基重排
氧化磷酸化
四氢呋喃
药物化学
硫黄
键裂
催化作用
甲烷氧化偶联
有机化学
分子
溶剂
生物化学
作者
Jiwei Wu,Yi Zhou,Yuchen Zhou,Chien‐Wei Chiang,Aiwen Lei
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-10-26
卷期号:7 (12): 8320-8323
被引量:183
标识
DOI:10.1021/acscatal.7b03551
摘要
A method for electrooxidative C(sp3)–H amination via intermolecular oxidative C(sp3)–H/N–H cross-coupling has been developed under metal- and oxidant-free conditions. The C(sp3)–H bonds adjacent to oxygen, nitrogen, and sulfur atoms could all react smoothly with various amines to give the corresponding products with moderate to good yields (30–93%). In addition, the C(sp3)–H bonds of benzylic and allylic are also tolerated in this reaction. A preliminary mechanistic study indicates that the C–H cleavage of tetrahydrofuran is probably not involved in the rate-determining step.
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