Hydrazones from hydroxy naphthaldehydes. Part 2. Condensations with aromatic N-aminoheterocycles and elucidation of tautomeric structures-Reference-Cited by-同舟云学术

Hydrazones from hydroxy naphthaldehydes. Part 2. Condensations with aromatic N-aminoheterocycles and elucidation of tautomeric structures

Published:2014-04 Issue:14 Volume:70 Page:2319-2329
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Martínez R. Fernando,Ávalos Martín,Babiano Reyes,Cintas Pedro,Light Mark E.,Jiménez José L.,Palacios Juan C.

Funder

Ministerio de Ciencia e Innovación

Junta de Extremadura

FEDER

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference62 articles.

1. Excited State Intramolecular Proton Transfer in Schiff Bases. Decay of the Locally Excited Enol State Observed by Femtosecond Resolved Fluorescence

2. The Nature of Solid-State N−H···O/O−H···N Tautomeric Competition in Resonant Systems. Intramolecular Proton Transfer in Low-Barrier Hydrogen Bonds Formed by the ···OC−CN−NH··· ⇄ ···HO−CC−NN··· Ketohydrazone−Azoenol System. A Variable-Temperature X-ray Crystallographic and DFT Computational Study

3. In general, Schiff bases originating from o-hydroxy-carbocycles and heterocycles have been reported with imine structures. For related studies involving 3-hydroxy-4-pyridinecarboxaldehyde derivatives:

4. Synthesis and spectroscopic properties of Schiff bases derived from 3-hydroxy-4-pyridinecarboxaldehyde

5. Syntheses and Structural Studies of Schiff Bases Involving Hydrogen Bonds

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