Reactivity of 1,2,3-triazoles towards sulfonyl chlorides. A novel approach to 1- and 2-sulfonyl-4-azolyl-1,2,3-triazoles

doi:10.1016/J.TET.2015.06.088

Paper

Reactivity of 1,2,3-triazoles towards sulfonyl chlorides. A novel approach to 1- and 2-sulfonyl-4-azolyl-1,2,3-triazoles

Published Sep 9, 2015 · T. Beryozkina, I. Efimov, W. Fabian

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17

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Abstract

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Study Snapshot

1,2,3-triazoles react with sulfonyl chlorides to form regioisomers of 1- and 2-substituted 1,2,3-triazoles, with the ratio of isomers influenced by the nature of the azolyl ring and the size of the substituent

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Reactivity of 1,2,3-triazoles towards sulfonyl chlorides. A novel approach to 1- and 2-sulfonyl-4-azolyl-1,2,3-triazoles

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