Paper

Synthesis of 2-arylbenzothiazoles via direct condensation between in situ generated 2-aminothiophenol from disulfide cleavage and carboxylic acids

Published Jun 14, 2017 · Felipe L. Coelho, L. Campo

Tetrahedron Letters

Citations

Influential Citations

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

This study presents a simple and efficient method for preparing 2-arylbenzothiazoles using disulfides and carboxylic acids, with moderate to good yields, and successfully tested on the amyloid probe 2-(4-aminophenyl)-6-methoxybenzothiazole.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Synthesis of 2-arylbenzothiazoles via direct condensation between in situ generated 2-aminothiophenol from disulfide cleavage and carboxylic acids

References

Citations