A new sulfonamide possessing strong carbonic anhydrase (CA) inhibitory properties has
been prepared by reaction of 5-amino-1, 3, 4-thiadiazole-2-sulfonamide with adamantyl-1 …

This study focused on the synthesis and characterization of hydrazide ligands and their
respective Pd (II) complexes and used high throughput screening to determine their α …

Reaction of five aromatic/heterocyclic sulfonamides containing free amino, groups with 5-
nitro-α-2-toluenesultone and diethyl pyrocarbonate, respectively, afforded novel inhibitors of …

Two acetazolamide (AAZ) complexes with ruthenium (II) η6-p-cymene chloride were
synthesised, characterised and tested for their inhibitory effects on several carbonic …

A series of organometallic acylhydrazones was prepared, incorporating Re (CO) 3, Mn (CO)
3 and ferrocenyl moieties, which were subsequently reacted with amino-sulfonamides in …

Reaction of three aromatic sulfonamides possessing a primary amino group, ie,
sulfanilamide, homosulfanilamide and p-aminoethyl-benzenesulfonamide with heterocyclic …

Sulfonamides represent an important class of biologically active compounds. A sulfonamide
possessing carbonic anhydrase (CA) inhibitory properties obtained from a pyrazole based …

Complexes containing the anions of 5-benzoylamido-l, 3, 4-thiadiazole-2-sulfonamide and 5-
(3-nitrobenzoylamido)-l, 3, 4-thiadiazole-2-sulfonamide as ligands, and main group metal …

The title compound was prepared by an improved variant of the literature procedure, and
metal complexes containing its anion and the following metal ions: Zn (II), Cd (II), Hg (II), Co …

Reaction of aromatic/heterocyclic sulfonamides containing a free amino group with triflic
anhydride afforded compounds possessing trifluoromethanesulfonamido moieties in their …