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A cascade reaction for regioselective construction of pyrazole-containing aliphatic sulfonyl fluorides.
Yang, Wen-Fei; Shu, Tao; Chen, Hong-Ru; Qin, Hua-Li; Tang, Haolin.
Afiliación
  • Yang WF; School of Chemistry, Chemical Engineering and Life Sciences; and State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China. qinhuali@whut.edu.cn.
  • Shu T; School of Chemistry, Chemical Engineering and Life Sciences; and State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China. qinhuali@whut.edu.cn.
  • Chen HR; School of Chemistry, Chemical Engineering and Life Sciences; and State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China. qinhuali@whut.edu.cn.
  • Qin HL; School of Chemistry, Chemical Engineering and Life Sciences; and State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China. qinhuali@whut.edu.cn.
  • Tang H; School of Chemistry, Chemical Engineering and Life Sciences; and State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China. qinhuali@whut.edu.cn.
Org Biomol Chem ; 20(17): 3506-3510, 2022 05 04.
Article en En | MEDLINE | ID: mdl-35420611
ABSTRACT
A copper-catalyzed cascade reaction of α-diazocarbonyl compounds with ethenesulfonyl fluoride (ESF) is developed, affording a variety of highly functionalized pyrazolyl aliphatic sulfonyl fluorides in good to excellent yields (66-98%). This transformation features broad substrates, exclusive regioselectivity, high atom economy and operational simplicity, thus providing a straightforward method for the direct construction of pyrazole-containing aliphatic sulfonyl fluorides, which will provide great applicable value in medicinal chemistry and other related disciplines.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ácidos Sulfínicos / Fluoruros Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ácidos Sulfínicos / Fluoruros Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: China