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Synthesis of Fully Substituted Difluoromethylpyrazoles by Cyclization of Difluoroacetohydrazonoyl Bromides with 2-Acylacetonitriles or Malononitrile.

Si-Wei WangJianzhong ZhangZhoubin DengYuyu LvDanfeng HuangKe-Hu WangJunJiao WangYulai Hu
Published in: The Journal of organic chemistry (2024)
A concise and efficient method for the construction of fully substituted difluoromethylpyrazoles is achieved by a cyclization reaction between difluoroacetohydrazonoyl bromides and 2-acylacetonitrile or malononitrile. The method features advantages such as mild reaction conditions, broad substrate scope, good product yields, and high regioselectivity.
Keyphrases
  • molecular docking
  • amino acid
  • structural basis