废止
炔烃
苯并咪唑
化学
异吲哚
合成子
催化作用
分子内力
毛竹
酰胺
立体化学
药物化学
有机化学
生物
生态学
竹子
作者
Ying‐Ti Huang,Indrajeet J. Barve,Ganesh P. Pawar,Chung‐Ming Sun
标识
DOI:10.1021/acs.joc.3c00937
摘要
A Rh(III)-catalyzed [4 + 1] cyclization of 2-arylbenzimidazoles with alkynoates through C-H activation/ortho-alkenylation/intramolecular annulation cascade to obtain benzimidazole-fused isoindoles is reported. The reaction of the Rh catalyst and internal alkyne ester provides benzo[4,5]imidazo[2,1-a]isoindole acetate exclusively. Conversely, internal alkyne amide participates in the annulation process in the presence of a Ru catalyst to provide benzo[4,5]imidazo[2,1-a]isoindole acetamide. The alkyne acts as a C1 synthon and undergoes [4 + 1] cyclization rather than traditional [4 + 2] annulation.
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