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I2/CF3CO2Ag-mediated iodolactonization of various allenoic acids to access versatile 6- to 9-membered ring vinylic iodolactones.
Bao, Xiaobo; Wang, Guoli; Dong, Xu; Zhu, Mengxiao; Yang, Lili; Zhu, Junjie; Shi, Qingyuan; Zhang, Hongzhen; Chen, Dongyin.
Afiliación
  • Bao X; College of Pharmacy, Jiangsu Vocational College of Medicine, Yancheng, 224005, China.
  • Wang G; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
  • Dong X; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
  • Zhu M; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
  • Yang L; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
  • Zhu J; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
  • Shi Q; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
  • Zhang H; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
  • Chen D; School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China. chendongyin@njmu.edu.cn.
Org Biomol Chem ; 22(12): 2443-2450, 2024 Mar 20.
Article en En | MEDLINE | ID: mdl-38416045
ABSTRACT
Medium-sized lactones are important structural units, but their synthesis remains a great challenge. Herein, we report I2/CF3CO2Ag-mediated iodolactonization of allenoic acids to synthesize various 6- to 9-membered ring vinylic iodolactones in 16-89% yield. This protocol not only develops a new cyclization strategy of allenoic acids, but also provides highly functionalized medium-sized lactones containing alkene and halogen groups.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China