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Silver-catalyzed cyclization of α-imino-oxy acids to fused tetralone derivatives.
Liu, Kai; Li, Feng; Wang, Jingjing; Zhang, Zhaowei; Du, Fengge; Su, Hanxiao; Wang, Yonghong; Yuan, Qingqing; Li, Fei; Wang, Teng.
Afiliação
  • Liu K; School of Petrochemical Engineering, Liaoning Petrochemical University, Fushun 113001, China. lnpulf@126.com.
  • Li F; College of Food Science and Pharmaceutical Engineering, Zaozhuang University, Zaozhuang 277160, China. lifeng20150720@163.com.
  • Wang J; College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.
  • Zhang Z; College of Food Science and Pharmaceutical Engineering, Zaozhuang University, Zaozhuang 277160, China. lifeng20150720@163.com.
  • Du F; College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.
  • Su H; College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.
  • Wang Y; College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.
  • Yuan Q; College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.
  • Li F; College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.
  • Wang T; College of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000, China.
Org Biomol Chem ; 21(13): 2700-2704, 2023 Mar 29.
Article em En | MEDLINE | ID: mdl-36912118
A silver-catalyzed intramolecular radical relay cyclization of α-imino-oxy acids under mild conditions has been described. This reaction offers facile access to a diverse range of fused tetralone derivatives with exquisite stereoselectivity in moderate to good yields (40-98%). Experimental studies show that the reaction undergoes a decarboxylation and acetone fragmentation/1,5-hydrogen atom transfer (HAT)/cyclization process.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article