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Zinc-Catalyzed Asymmetric Cascade Michael/Acyl Transfer Reaction between α-Hydroxy Aryl Ketones and Enynones.
Yan, Hang; Zhang, Cui; Han, Jiao-Jiao; Du, Si-Si; Hua, Yuan-Zhao; Wang, Min-Can; Mei, Guang-Jian; Jia, Shi-Kun.
Afiliación
  • Yan H; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
  • Zhang C; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
  • Han JJ; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
  • Du SS; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
  • Hua YZ; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
  • Wang MC; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
  • Mei GJ; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
  • Jia SK; College of Chemistry and Institute of Green Catalysis, Zhengzhou University, Zhengzhou, Henan 450000, People's Republic of China.
Org Lett ; 25(11): 1918-1923, 2023 Mar 24.
Article en En | MEDLINE | ID: mdl-36926928
We described herein a neoteric enantioselective cascade Michael/acyl transfer reaction of enynones and α-hydroxy aryl ketones catalyzed by dinuclear zinc cooperative catalysis. A series of structurally diverse chiral 1,5-dicarbonyl compounds were synthesized in good yields with excellent stereoselectivities. This strategy features broad substrate scope, high atom economy, as well as enynones as efficient electrophilic acyl transfer reagents in asymmetric cascade reactions for the first time.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos