A new strategy for the synthesis of amides has been developed using sulfur-mediated decarboxylative coupling of cinnamic acids with amines via oxidative cleavage of the C═C bond.
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http://dx.doi.org/10.1021/acs.joc.4c00669 | DOI Listing |
J Org Chem
July 2024
Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi 221005, India.
A new strategy for the synthesis of amides has been developed using sulfur-mediated decarboxylative coupling of cinnamic acids with amines via oxidative cleavage of the C═C bond.
View Article and Find Full Text PDFEnviron Sci Technol
November 2022
School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.
Incomplete mineralization of antibiotics in biological sludge systems poses a risk to the environment. In this study, the toxicity associated with ciprofloxacin (CIP) biodegradation in activated sludge (AS), anaerobic methanogenic sludge (AnMS), and sulfur-mediated sludge (SmS) systems was examined via long-term bioreactor tests and a series of bioassays. The AS and AnMS systems were susceptible to CIP and its biotransformation products (TPs) and exhibited performance deterioration, while the SmS system exhibited high tolerance against the toxicity of CIP and its TPs along with excellent pollutant removal.
View Article and Find Full Text PDFOrg Lett
February 2015
Department of Chemistry (Centre of Advanced Study), Faculty of Science, Banaras Hindu University, Varanasi-221005, India.
A decarboxylative redox cyclization strategy has been developed for the synthesis of 2-substituted benzothiazoles by the reaction of o-chloronitroarenes and arylacetic acids in the presence of elemental sulfur/N-methylmorpholine under metal- and solvent-free conditions.
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