分子内力
铱
化学
胺化
电泳剂
组合化学
催化作用
亲电取代
亲电芳香族取代
立体化学
药物化学
有机化学
作者
Yeongyu Hwang,Yoonsu Park,Yeong Bum Kim,Dongwook Kim,Sukbok Chang
标识
DOI:10.1002/anie.201808892
摘要
Abstract Two mechanistic pathways, that is, electrocyclization and electrophilic aromatic substitution, are operative in most intramolecular C−H amination reactions proceeding by metal nitrenoid catalysis. Reported here is an alternative mechanistic scaffold leading to benzofused δ‐lactams selectively. Integrated experimental and computational analysis revealed that the reaction proceeds by a key spirocyclization step followed by a skeletal rearrangement. Based on this mechanistic insight, a new synthetic route to spirolactams has been developed.
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