Article thumbnail
Location of Repository

Elemental Sulfur Mediated Decarboxylative Redox Cyclization Reaction of <i>o</i>‑Chloronitroarenes and Arylacetic Acids

By Tirumaleswararao Guntreddi (1652185), Rajeshwer Vanjari (1652188) and Krishna Nand Singh (1652182)


A decarboxylative redox cyclization strategy has been developed for the synthesis of 2-substituted benzothiazoles by the reaction of <i>o</i>-chloronitroarenes and arylacetic acids in the presence of elemental sulfur/<i>N</i>-methylmorpholine under metal- and solvent-free conditions

Topics: Biophysics, Biochemistry, Medicine, Neuroscience, Computational Biology, Chemical Sciences not elsewhere classified, presence, Elemental Sulfur Mediated Decarboxylative Redox Cyclization Reaction, benzothiazole, synthesis, arylacetic acids, sulfur, Arylacetic AcidsA decarboxylative redox cyclization strategy
Year: 2015
DOI identifier: 10.1021/acs.orglett.5b00079.s001
OAI identifier:
Provided by: FigShare
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • (external link)
  • Suggested articles

    To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.