We outline herein the protocols developed to synthesize a diverse
array of organic compounds: from carbimidothioates, we successfully synthesized
\(\beta\)-enaminones, 1,5-diaryl-1H-tetrazoles, and 1,3,4-oxadiazoles, each of
which has potential applications in various fields including pharmaceuticals
and materials science. From carbamimidothioates, our synthesis yielded both
imidazoles and 1,5-disubstituted tetrazoles, thus expanding the scope of these
nitrogen-rich heterocycles in medicinal chemistry. Additionally, the
transformation of 2-oxo-ethanimidothioates into 2-amino-3-aryl-quinoxalines
highlights a novel pathway for producing compounds that could be valuable in
light-emitting devices and as pharmacological agents. This detailed
investigation not only advances the field of synthetic organic chemistry but
also sets the stage for future innovations in the synthesis and application of
heterocyclic compounds.
Author(s)
Details
Toreshettahally
R. Swaroop
Department of Studies in Organic Chemistry, University of Mysore,
Manasagangotri, Mysuru - 570 006, Karnataka, India.
Muddegowda
Umashankara
Department of Chemistry, Karnataka State Open University,
Muktagangotri, Mysuru - 570 006, Karnataka, India.
Kanchugarakoppal
S. Rangappa
Institution of Excellence, University of Mysore, Manasagangotri,
Mysuru - 570 006, Karnataka, India.
Please see the book here:- https://doi.org/10.9734/bpi/rdcbr/v5/1329
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