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Silver-mediated radical oxytrifluoromethylation of unsaturated carboxylic acids for the synthesis of γ-trifluoromethylthio lactones.
Ru-Jian, Yu; Zhang, Chun-Yan; Hai-Yan, Huang; Pei, Wang; Fu, Wen-Yu; Cheng, Jian-Xin; Xiong, Yan-Shi.
Afiliação
  • Ru-Jian Y; School of Pharmacy, Jiangxi Science & Technology Normal University, Nanchang, 330013, Jiangxi, P. R. China. xiongys1214@163.com.
  • Zhang CY; School of Pharmacy, Jiangxi Science & Technology Normal University, Nanchang, 330013, Jiangxi, P. R. China. xiongys1214@163.com.
  • Hai-Yan H; School of Pharmacy, Jiangxi Science & Technology Normal University, Nanchang, 330013, Jiangxi, P. R. China. xiongys1214@163.com.
  • Pei W; School of Pharmacy, Jiangxi Science & Technology Normal University, Nanchang, 330013, Jiangxi, P. R. China. xiongys1214@163.com.
  • Fu WY; School of Pharmacy, Jiangxi Science & Technology Normal University, Nanchang, 330013, Jiangxi, P. R. China. xiongys1214@163.com.
  • Cheng JX; School of Pharmacy, Jiangxi Science & Technology Normal University, Nanchang, 330013, Jiangxi, P. R. China. xiongys1214@163.com.
  • Xiong YS; School of Pharmacy, Jiangxi Science & Technology Normal University, Nanchang, 330013, Jiangxi, P. R. China. xiongys1214@163.com.
Org Biomol Chem ; 20(10): 2109-2114, 2022 03 09.
Article em En | MEDLINE | ID: mdl-35199820
An efficient silver-mediated oxidative trifluoromethylthiolation of unsaturated carboxylic acids to construct trifluoromethylthiol-containing lactones has been disclosed. In this protocol no metal-catalysts was added, and preliminary mechanism investigations suggested that a free-radical pathway should be involved in the process. High functional group tolerance and excellent yields were demonstrated by the efficient preparation of a wide range of γ-trifluoromethylthiolated phthalides.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article