Bis(methoxycarbonyl)[2.2](2,5)pyridinophanes as nicotinamide coenzyme models
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Enhanced rates of dihydropyridine to pyridinium hydrogen transfer in complexes of an active macrocyclic receptor molecule
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3. Intramolecular redox systems related to NAD/NADH, part 1. A kinetic study of intramolecular hydride exchange by 1-H-spin saturation transfer
4. Multicenter organic redox systems composed of bis(1,4-dihydronicotinamides): optimal conformation for intramolecular electronic interaction
5. 1,8‐Dipyrenylnaphthalenes: Syntheses, Molecular Structure, and Spectroscopic Properties
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1. Synthetic Strategy toward Skeletal Diversity via Solid-Supported, Otherwise Unstable Reactive Intermediates;Angewandte Chemie International Edition;2004-03-19
2. Theoretical analysis of the photoinduced electron transfer in porphyrin—quinone cyclophanes;Chemical Physics Letters;1992-03
3. Electron impact and chemical ionization mass spectra of bis(methoxycarbonyl) [2.2](2,5)pyridinophanes. Formation of quinolizinium ions under electron impact;Organic Mass Spectrometry;1986-06
4. ChemInform Abstract: Bis(methoxycarbonyl)[2.2](2,5)pyridinophanes as Nicotinamide Coenzyme Models.;Chemischer Informationsdienst;1986-04-22
5. Multistep Reversible Redox Systems, XLVII1)N,N′-Dicyanoquinonediimines - A New Class of Compounds, II: Comparison of Redox Properties with those of Quinones and Tetracyanoquinodimethanes;Liebigs Annalen der Chemie;1986-01-14
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