Synthesis, tautomeric forms, specific intermolecular interactions, and lipophilicity of methylated 6-hydroxypyridazine-3-carboxylic acid and its 4,5-dihydro analogs

doi:10.1016/J.MOLSTRUC.2011.05.016

Paper

Synthesis, tautomeric forms, specific intermolecular interactions, and lipophilicity of methylated 6-hydroxypyridazine-3-carboxylic acid and its 4,5-dihydro analogs

Published Jul 13, 2011 · A. Katrusiak, Paweł Piechowiak, A. Katrusiak

Journal of Molecular Structure

Q2 SJR score

2

Citations

0

Influential Citations

Full textSemantic Scholar

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

Methylated 6-hydroxypyridazine-3-carboxylic acid and its 4,5-dihydro analogs exhibit increased lipophilicity due to the formation of CHO bonds, affecting intermolecular interactions and tautomer formation.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Sign up to use Study Snapshot

Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.

Create an account

Synthesis, tautomeric forms, specific intermolecular interactions, and lipophilicity of methylated 6-hydroxypyridazine-3-carboxylic acid and its 4,5-dihydro analogs

Sign up to use Study Snapshot

References

Citations