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Divergent synthesis of 1,3,5-tri and 1,3-disubstituted pyrazoles under transition metal-free conditions.
Ma, Liyao; Ou, Pengcheng; Huang, Xueliang.
Afiliação
  • Ma L; College of Chemistry, Fuzhou University, Fuzhou 350116, China and Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter, Fujian College, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China. huangxl@fjirsm.ac.cn.
  • Ou P; College of Chemistry, Fuzhou University, Fuzhou 350116, China and Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter, Fujian College, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China. huangxl@fjirsm.ac.cn.
  • Huang X; Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter, Fujian College, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China. huangxl@fjirsm.ac.cn.
Org Biomol Chem ; 18(33): 6487-6491, 2020 08 26.
Article em En | MEDLINE | ID: mdl-32785327
ABSTRACT
Pyrazole cores are common structural motifs existing in various agrochemicals and pharmaceuticals. Herein, a transition metal-free, three-component reaction of arylaldehydes, ethyl acrylate and N-tosylhydrazones is described, which leads to the formation of 1,3,5-trisubstituted and 1,3-disubstituted pyrazoles divergently under slightly different conditions.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article