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Synthesis of 3-Azabicyclo[m.2.0] Ring Systems via a Copper-Catalyzed Cascade Reaction of Diazo Compounds with 1,n-Allenynes.
He, Min; Chen, Nuan; Liu, Lala; Zhu, Yuqi; Li, Qing; Li, Hongguang; Lang, Ming; Wang, Jian; Peng, Shiyong.
Afiliação
  • He M; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, People's Republic of China.
  • Chen N; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, People's Republic of China.
  • Liu L; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, People's Republic of China.
  • Zhu Y; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, People's Republic of China.
  • Li Q; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, People's Republic of China.
  • Li H; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, People's Republic of China.
  • Lang M; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, People's Republic of China.
  • Wang J; School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 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.
J Org Chem ; 85(6): 4418-4429, 2020 03 20.
Article em En | MEDLINE | ID: mdl-32091906
A copper-catalyzed cascade reaction of diazo compounds with 1,n-allenynes (n = 6,7) was reported, which provides efficient access to various functionalized 3-azabicyclo[m.2.0] frameworks (m = 5,6) in moderate to excellent yields under mild reaction conditions. The reaction proceeds through intermolecular cross-coupling to form bisallene intermediates, followed by subsequent intramolecular [2+2] cycloaddition.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article