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Direct C3 Carbamoylation of 2H-Indazoles

  • Vighneshwar Shridhar Bhat
  • , Anna Lee*
  • *Corresponding author for this work
  • Jeonbuk National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

We developed a novel method for direct C3 carbamoylation of 2H-indazoles using oxamic acids as carbamoyl radical sources. In the presence of ammonium persulfate, carbamoyl radicals were generated from oxamic acids, then used for further reactions with 2H-indazoles to afford the desired products. The reaction proceeds under metal- and catalyst-free conditions. This simple process allows for the efficient synthesis of C3 carbamoylated 2H-indazoles, which are important scaffolds in organic synthesis.

Original languageEnglish
Pages (from-to)3382-3385
Number of pages4
JournalEuropean Journal of Organic Chemistry
Volume2021
Issue number23
DOIs
StatePublished - 2021.06.21

Keywords

  • 2H-Indazoles
  • Carbamoylation
  • Minisci reaction
  • Radical reaction
  • Synthetic methods

Quacquarelli Symonds(QS) Subject Topics

  • Engineering - Petroleum
  • Chemistry

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