<p>The novel approach to the preparation of
imidazole-substituted cyclic iodonium salts has been developed via oxidative
cyclization of 1-phenyl-5-iodoimidazole
using cheap and available Oxone<sup>®</sup>/H<sub>2</sub>SO<sub>4</sub>
oxidative system. The structure of newly prepared compounds has been proved by
X-ray monocrystal diffractometry revealing the characteristic surface features
for cyclic iodonium salts. The prepared compounds demonstrated the high
reactivity in the heterocyclization reactions with elemental sulfur affording benzo[5,1-<i>b</i>]imidazothiazoles
with good yields.</p>
<p>The novel approach to the preparation of
imidazole-substituted cyclic iodonium salts has been developed via oxidative
cyclization of 1-phenyl-5-iodoimidazole
using cheap and available Oxone<sup>®</sup>/H<sub>2</sub>SO<sub>4</sub>
oxidative system. The structure of newly prepared compounds has been proved by
X-ray monocrystal diffractometry revealing the characteristic surface features
for cyclic iodonium salts. The prepared compounds demonstrated the high
reactivity in the heterocyclization reactions with elemental sulfur affording benzo[5,1-<i>b</i>]imidazothiazoles
with good yields.</p>
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