Paper
Synthesis of certain 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and thieno[2,3-b]thiophene-2-sulfonamide 6,6-dioxides
Published 1999 · Hwang-Hsing Chen, J. May, V. Lynch
Journal of Heterocyclic Chemistry
Q3 SJR score
9
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0
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Abstract
A series of the title compounds were prepared for evaluation as inhibitors of carbonic anhydrase II. Oxidation of 5-substituted thieno[2,3-b]thiophene-2-sulfonamides provided the first examples of thiophene[2,3-b]thiophene-2-sulfonarnide 6,6-dioxides. These cyclic vinyl sulfones readily underwent addi tion to give predominately that 4,5-cis addition product.
Study Snapshot
5-substituted thieno[2,3-b]thiophene-2-sulfonamides show potential as inhibitors of carbonic anhydrase II, with 4,5-cis addition product being the most abundant product.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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