Publication:
CATALYST-FREE SYNTHESIS OF A SERIES OF DIARYLSUFONYLUREAS

dc.contributor.authorSIVAKAMI JAYA SEELAN
dc.date.accessioned2023-10-06T15:31:55Z
dc.date.available2023-10-06T15:31:55Z
dc.date.issued2023
dc.description.abstractIn comparison to traditional organic synthesis, catalyst-free synthetic techniques provide several advantages and have been proved to be environmentally friendly. Here, a facile catalyst-free procedure for the synthesis of derivatives of diarylsulfonylureas was developed. The simple process involves reacting p-toluenesulfonyl isocyanate with various substituted primary amines in the presence of dichloromethane as the solvent at room temperature to produce the desired diarylsulfonylureas derivatives. Nine compounds with up to 94% yield have been synthesized successfully through this protocol. These products' structures were characterised using a variety of techniques, including fourier-transform infrared spectroscopy, mass spectroscopy, nuclear magnetic resonance spectroscopy, physical analysis, and melting point. Overall, this method has many benefits, including convenient room temperature synthesis, a straightforward workup procedure, rapid reaction times, and quantifiable reaction yields. Keywords: Diarylsulfonylureas, Green Chemistry, Catalyst-Free, Room Temperature synthesisen_US
dc.identifier.urihttps://hdl.handle.net/20.500.14377/32188
dc.language.isoenen_US
dc.publisherInternational Medical Universityen_US
dc.subjectChemistry Techniques, Syntheticen_US
dc.subjectMagnetic Resonance Spectroscopyen_US
dc.subjectSpectroscopy, Fourier Transform Infrareden_US
dc.subjectEnvironmental Pollutantsen_US
dc.subjectPhotosynthesisen_US
dc.titleCATALYST-FREE SYNTHESIS OF A SERIES OF DIARYLSUFONYLUREASen_US
dc.typeThesis
dspace.entity.typePublication
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