Direct and Enantioselective Synthesis of N-H-Free 1,5-Benzodiazepin-2-ones by an N-Heterocyclic Carbene Catalyzed [3+4] Annulation Reaction.

Fang, Chao; Cao, Jing; Sun, Kewen; Zhu, Jindong; Lu, Tao; Du, Ding

Fang, Chao; Cao, Jing; Sun, Kewen; Zhu, Jindong; Lu, Tao; Du, Ding.

Afiliación

Fang C; State Key Laboratory of Natural Medicines, Department of Organic Chemistry, China Pharmaceutical University, Nanjing, 210009, P. R. China.
Cao J; State Key Laboratory of Natural Medicines, Department of Organic Chemistry, China Pharmaceutical University, Nanjing, 210009, P. R. China.
Sun K; State Key Laboratory of Natural Medicines, Department of Organic Chemistry, China Pharmaceutical University, Nanjing, 210009, P. R. China.
Zhu J; State Key Laboratory of Natural Medicines, Department of Organic Chemistry, China Pharmaceutical University, Nanjing, 210009, P. R. China.
Lu T; State Key Laboratory of Natural Medicines, Department of Organic Chemistry, China Pharmaceutical University, Nanjing, 210009, P. R. China.
Du D; State Key Laboratory of Natural Medicines, Department of Organic Chemistry, China Pharmaceutical University, Nanjing, 210009, P. R. China.

Chemistry ; 24(9): 2103-2108, 2018 Feb 09.

Article en En | MEDLINE | ID: mdl-29236349

Palabras clave

annulation; asymmetric synthesis; benzodiazepinone; carbenes; unsaturated acylazolium

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2018 Tipo del documento: Article Pais de publicación: Alemania

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