双环分子
酰胺
化学
内酰胺
喹啉
亲核细胞
组合化学
立体化学
药物化学
有机化学
催化作用
作者
Zhuang Xiong,Chunmei Hu,Wenjian Zhu,Simin Wu,Dan Wang,Yang Liu,Jing Lin,Suqin Guo,Jia‐Qiang Wu,Xue-Tao Xu
标识
DOI:10.1021/acs.joc.3c00405
摘要
Efficient access to the synthesis of lactam-derived quinoline through a bicyclic amidine-triggered cyclization reaction from readily prepared o-alkynylisocyanobenzenes has been developed. The reaction was initiated by nucleophilic attack of the bicyclic amidines to o-alkynylisocyanobenzenes, subsequently with intramolecular cyclization to produce a DBU-quinoline-based amidinium salt, followed by hydrolysis to afford the lactam-derived quinoline in moderate to good yields.
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