合成子
化学
废止
表面改性
级联
烷基
劈理(地质)
电化学
组合化学
分子间力
四级碳
级联反应
激进的
键裂
有机化学
氧化裂解
反应条件
氧化磷酸化
立体化学
高分子化学
光化学
自由基反应
作者
Xin-Yao LIU,Gui‐Fen Lv,Qing Sun,Jin‐Heng Li,Yang Li
标识
DOI:10.1021/acs.orglett.6c04666
摘要
Abstract A general electrochemical intermolecular cascade annulation between N-arylacrylamides and 1,3-dicarbonyl compounds through C(sp3)–H/C(sp2)–H functionalization and 1,4-aryl migration has been developed. This protocol employs 1,3-dicarbonyl compounds as C1 synthons that undergo [4+1] carboannulation, delivering diverse functionalized indanes with two distinct quaternary carbon centers under noble-metal- and external-oxidant-free conditions. Control experiments indicate that the reaction proceeds via a sequential cascade of oxidative C(sp3)–H cleavage to generate an alkyl radical, radical addition across the C═C bond, 1,4-aryl migration, a further oxidative C(sp3)–H cleavage to form another alkyl radical, [4+1] annulation, and deprotonation.
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