Direct selenosulfonylation of unsaturated compounds: a review
TH Abdtawfeeq, EA Mahmood, SB Azimi, MM Kadhim… - RSC …, 2022 - pubs.rsc.org
In this review, we have discussed recent developments on the direct selenosulfonylation of
unsaturated compounds which lead to the formation of two new carbon-sulfur and carbon …
unsaturated compounds which lead to the formation of two new carbon-sulfur and carbon …
Hydrazinosulfonylation of aryl electrophiles: a straightforward approach for the synthesis of aryl N-aminosulfonamides
CY Hsu, AKO Aldulaimi, H Bahir, AH Adhab… - RSC …, 2023 - pubs.rsc.org
In recent years, the direct hydrazinosulfonylation of aryl electrophiles with SO2 and
hydrazines has emerged as an efficient and versatile method for the synthesis of aryl N …
hydrazines has emerged as an efficient and versatile method for the synthesis of aryl N …
4-Cyanamidobenzenesulfonamide derivatives: a novel class of human and bacterial carbonic anhydrase inhibitors
A one-pot two-step protocol was developed for the synthesis of a series of novel 4-
cyanamidobenzenesulfonamides from easily accessible methyl (4-sulfamoylphenyl) …
cyanamidobenzenesulfonamides from easily accessible methyl (4-sulfamoylphenyl) …
Benzenesulfonamides incorporating hydantoin moieties effectively inhibit eukaryoticand human carbonic anhydrases
A series of novel 1-(4-benzenesulfonamide)-3-alkyl/benzyl-hydantoin derivatives were
synthesized and evaluated for the inhibition of eukaryotic and human carbonic anhydrases …
synthesized and evaluated for the inhibition of eukaryotic and human carbonic anhydrases …
2-((1H-Benzo [d] imidazol-2-yl) amino) benzo [d] thiazole-6-sulphonamides: a class of carbonic anhydrase II and VII-selective inhibitors
M Abdoli, CT Supuran… - Journal of Enzyme …, 2023 - Taylor & Francis
A small library of substituted cyclic guanidine incorporated benzothiazole-6-sulphonamides
was synthesized. All obtained compounds were investigated for their inhibitory activity …
was synthesized. All obtained compounds were investigated for their inhibitory activity …
Novel thiazolone-benzenesulphonamide inhibitors of human and bacterial carbonic anhydrases
A small library of novel thiazolone-benzenesulphonamides has been prepared and
evaluated for their ability to inhibit three human cytosolic carbonic anhydrases (hCA I, hCA II …
evaluated for their ability to inhibit three human cytosolic carbonic anhydrases (hCA I, hCA II …
Investigation of novel alkyl/benzyl (4-sulphamoylphenyl) carbamimidothioates as carbonic anhydrase inhibitors
A library of novel alkyl/benzyl (4-sulphamoylphenyl) carbamimidothioates was synthesised
by selective S-alkylation of the easily accessible 4-thioureidobenzenesulphonamide. The …
by selective S-alkylation of the easily accessible 4-thioureidobenzenesulphonamide. The …
Inhibition studies on carbonic anhydrase isoforms I, II, IX, and XII with a series of sulfaguanidines
Two novel sulfaguanidine series, six N‐(N, N′‐dialkyl/dibenzyl‐carbamimidoyl)
benzenesulfonamide derivatives and nine N‐(N‐alkyl/benzyl‐carbamimidoyl) …
benzenesulfonamide derivatives and nine N‐(N‐alkyl/benzyl‐carbamimidoyl) …
Inhibition Profiles of Some Novel Sulfonamide-Incorporated α-Aminophosphonates on Human Carbonic Anhydrases
A series of hitherto unknown sulfonamide-incorporated α-aminophosphonate derivatives
were synthesized through the one-pot, two-step FeCl3-catalyzed coupling of 4 …
were synthesized through the one-pot, two-step FeCl3-catalyzed coupling of 4 …
Synthesis and carbonic anhydrase I, II, IX, and XII inhibition studies with a series of cyclic sulfonyl guanidines
A series of thirteen cyclic sulfonyl guanidines were prepared and evaluated against tumor‐
associated human (h) carbonic anhydrase (CA, EC 4.2. 1.1) isoforms hCA IX and hCA XII, as …
associated human (h) carbonic anhydrase (CA, EC 4.2. 1.1) isoforms hCA IX and hCA XII, as …