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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)

Abstract

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: oai:figshare.com:article/2194294
Provided by: FigShare
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