Elemental Sulfur Mediated Decarboxylative Redox Cyclization Reaction of <i>o</i>‑Chloronitroarenes and Arylacetic Acids
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- Text
- Journal contribution
- 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
Similar works
This paper was published in FigShare.
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