A silver-mediated radical process of ß-keto sulfones for the synthesis of 2,3-diacyl furans.

Fan, Jian; Zu, Yanhong; Zheng, Zhimin; Song, Lulu; Wang, Yating; Zhou, Zhou; Liu, Yujun; Xu, Shuwen

Fan, Jian; Zu, Yanhong; Zheng, Zhimin; Song, Lulu; Wang, Yating; Zhou, Zhou; Liu, Yujun; Xu, Shuwen.

Afiliação

Fan J; Anhui Academy of Science and Technology, Hefei 230088, China. jianF@ahnu.edu.cn.
Zu Y; Anhui Academy of Science and Technology, Hefei 230088, China. jianF@ahnu.edu.cn.
Zheng Z; University of Science and Technology of China, Hefei 230026, China.
Song L; Anhui Academy of Science and Technology, Hefei 230088, China. jianF@ahnu.edu.cn.
Wang Y; Anhui Academy of Science and Technology, Hefei 230088, China. jianF@ahnu.edu.cn.
Zhou Z; Anhui Academy of Science and Technology, Hefei 230088, China. jianF@ahnu.edu.cn.
Liu Y; Anhui Academy of Science and Technology, Hefei 230088, China. jianF@ahnu.edu.cn.
Xu S; Anhui Academy of Science and Technology, Hefei 230088, China. jianF@ahnu.edu.cn.

Org Biomol Chem ; 22(9): 1770-1774, 2024 Feb 28.

Article em En | MEDLINE | ID: mdl-38324332

ABSTRACT

ABSTRACT

A facile and efficient method for constructing 2,3-diacyl trisubstituted furans via a silver-mediated radical process of ß-keto sulfones is developed. The reaction mechanism has been carefully investigated, revealing that the transformation proceeds through a radical pathway, leading to moderate to good yields of desired products.

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

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