Phosphine Oxide-Promoted Rh(I)-Catalyzed C-H Cyclization of Benzimidazoles with Alkenes

被引:2
作者
Lu, Mingzhen [1 ]
Xu, Weiwei [1 ]
Ye, Mengchun [1 ,2 ]
机构
[1] Nankai Univ, Coll Chem, Frontiers Sci Ctr New Organ Matter, State Key Lab Elemento Organ Chem, Tianjin 300071, Peoples R China
[2] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
基金
中国国家自然科学基金;
关键词
rhodium; C-H activation; benzimidazole; bimetal; phosphine oxide; BOND ACTIVATION; FUNCTIONALIZATION; HETEROCYCLES; SILYLATION; COMPLEXES;
D O I
10.3390/molecules28020736
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ligands play a critical role in promoting transition-metal-catalyzed C-H activation reactions. However, owing to high sensitivity of the reactivity of C-H activation to metal catalysts, the development of effective ligands has been a formidable challenge in the field. Rh(I)-catalyzed C-H cyclization of benzimidazoles with alkenes has been faced with low reactivity, often requiring very harsh conditions. To address this challenge, a phosphine oxide-enabled Rh(I)-Al bimetallic catalyst was developed for the reaction, significantly promoting the reactivity and allowing the reaction to run at 120 degrees C with up to 97% yield.
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页数:10
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