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B(C6F5)3-Catalyzed Formal (n + 3) (n = 5 and 6) Cycloaddition of Bicyclo[1.1.0]butanes to Medium Bicyclo[n.1.1]alkanes.
Yang, Liangliang; Wang, Haiyang; Lang, Ming; Wang, Jian; Peng, Shiyong.
Afiliación
  • Yang L; School of Pharmacy and Food Engineering, Wuyi University, Jiangmen, Guangdong 529020, People's Republic of China.
  • Wang H; School of Pharmacy and Food Engineering, Wuyi University, Jiangmen, Guangdong 529020, People's Republic of China.
  • Lang M; School of Pharmacy and Food Engineering, Wuyi University, Jiangmen, Guangdong 529020, People's Republic of China.
  • Wang J; School of Pharmacy and Food Engineering, Wuyi University, Jiangmen, Guangdong 529020, People's Republic of China.
  • Peng S; School of Pharmaceutical Sciences, Key Laboratory of Bioorganic Phosphorous Chemistry & Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, People's Republic of China.
Org Lett ; 26(19): 4104-4110, 2024 May 17.
Article en En | MEDLINE | ID: mdl-38700913
ABSTRACT
Herein, a B(C6F5)3-catalyzed formal (n + 3) (n = 5 and 6) cycloaddition of bicyclo[1.1.0]butanes (BCBs) with imidazolidines/hexahydropyrimidines is described. The reaction provides a modular, atom-economical, and efficient strategy to two libraries of synthetically challenging medium-bridged rings, 2,5-diazabicyclo[5.1.1]nonanes and 2,6-diazabicyclo[6.1.1]decanes, in moderate to excellent yields. This reaction also features simple operation, mild reaction conditions, and broad substrate scope. A scale-up experiment and various synthetic transformations of products further highlight the synthetic utility.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article
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