Synthesis and spectroscopic study of aminals derived from 2-aminopyridine and 3-aminopyridine

doi:10.1016/0022-2860(86)85152-3

Paper

Synthesis and spectroscopic study of aminals derived from 2-aminopyridine and 3-aminopyridine

Published Mar 1, 1986 · I. Iriepa, A. Lorente, E. Gálvez

Journal of Molecular Structure

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Abstract

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Study Snapshot

Aminals derived from 2-aminopyridine and 3-aminopyridine exhibit unusual stability due to intermolecular hydrogen bonding, contributing to their unusual IR and 1H NMR spectra.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

Synthesis and spectroscopic study of aminals derived from 2-aminopyridine and 3-aminopyridine

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References

Citations

NHC-Catalyzed Aza-Benzoin Condensation of N,N'-Dipyridin-2-yl Aminals with Aldehydes.

The NHC-catalyzed aza-benzoin reaction effectively synthesizes -amino ketones with up to 99% yield, offering potential for synthetic utility and bioactivities.

Designed synthesis of CO2-promoted copper(II) coordination polymers: synthesis, structural and spectroscopic characterization, and studies of versatile functional properties.

CO2-promoted Cu(II) coordination polymers show diverse functional properties, including mesoporosity and wide temperature range semiconductor activity.