Paper
The chemistry of thiamine: Studies on the dimerization of thiazolium salts
Published Mar 1, 1987 · M. Doughty, G. E. Risinger
Bioorganic Chemistry
Q1 SJR score
12
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0
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Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Thiazolium salts with electron-withdrawing substituents can produce stable rearranged dimers, demonstrating their nucleophilic carbene nature in aprotic basic solutions.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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