NMR study of conformation and isomerization of aryl- and heteroarylaldehyde 4-tert-butylphenoxyacetylhydrazones

doi:10.1016/J.MOLSTRUC.2005.11.018

Paper

NMR study of conformation and isomerization of aryl- and heteroarylaldehyde 4-tert-butylphenoxyacetylhydrazones

Published May 8, 2006 · V. Syakaev, S. Podyachev, B. I. Buzykin

Journal of Molecular Structure

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98

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2

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Abstract

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Study Snapshot

Nitrogen-carbonyl bond rotation leads to the existence of rotamers in 4-tert-butylphenoxyacetylhydrazones, with E/Z isomerization found only for pyridin-2-carbaldehyde.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

NMR study of conformation and isomerization of aryl- and heteroarylaldehyde 4-tert-butylphenoxyacetylhydrazones

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