Asymmetric Hydrogenation of Cyclic Imines of Benzoazepines and Benzodiazepines with Chiral, Cationic Ruthenium–Diamine Catalysts
Zhusheng Yang, Ziyuan Ding, Fei Chen, Yan‐Mei He, Nianfa Yang, Qing‐Hua Fan
Abstract
Zhusheng Yang, Ziyuan Ding, Fei Chen, Yan‐Mei He, Nianfa Yang, Qing‐Hua Fan
Abstract
A method for the highly enantioselective hydrogenation of diverse seven‐membered N‐containing heterocycles, including 2,4‐diaryl‐3H‐benzo[b]azepines, racemic 2,2,4‐trisubstituted 2,3‐dihydrobenzo[b][1,4]diazepines, and 4‐substituted 1H‐benzo[b][1,4]diazepin‐2(3H)‐ones by using chiral, cationic ruthenium–diamine catalysts was developed. Reversal of enantioselectivity was observed for all of these substrates simply by changing the achiral counteranion of the catalyst. This method thus provided facile access to both enantiomers of these optically pure seven‐membered heterocycles.
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A method for the highly enantioselective hydrogenation of diverse seven‐membered N‐containing heterocycles, including 2,4‐diaryl‐3H‐benzo[b]azepines, racemic 2,2,4‐trisubstituted 2,3‐dihydrobenzo[b][1,4]diazepines, and 4‐substituted 1H‐benzo[b][1,4]diazepin‐2(3H)‐ones by using chiral, cationic ruthenium–diamine catalysts was developed. Reversal of enantioselectivity was observed for all of these substrates simply by changing the achiral counteranion of the catalyst. This method thus provided facile access to both enantiomers of these optically pure seven‐membered heterocycles.
Key concepts: Enantioselective synthesis, Chemistry, Ruthenium, Cationic polymerization, Diamine, Asymmetric hydrogenation, Catalysis, Enantiomer