Oxidative Reactivity of S-Nitrosoglutathione with Hantzsch 1,4-Dihydropyridine
Organic Letters2000Vol. 2(6), pp. 741–742
Citations Over TimeTop 19% of 2000 papers
Abstract
S-Nitrosoglutathione oxidized 4-substituted Hantzsch 1,4-dihydropyridines in CH3CN/H2O or CH3CN/phosphate aqueous buffer solution to give aromatic products in various yields.
Related Papers
- → Theoretical study on the effective dehydrochlorination of 1,2-dichloroethane catalyzed by tetraalkylphosphonium chlorides: electrostatically controlled reactivity(2018)5 cited
- → ChemInform Abstract: New Aspects in the Reaction of Azomethines with Cyclic CH‐Acidic Compounds.(1992)
- → ChemInform Abstract: REACTIVITY OF OXOMOLYBDENUM(VI), ‐(V), AND ‐(IV) COMPOUNDS AS CONTROLLED BY SULFUR CHELATE LIGANDS(1979)
- → ChemInform Abstract: Oxidative Phosphorylation of α‐Hydroxy Nitriles Under the Conditions of the Atherton‐Todd Reaction.(1994)
- → ChemInform Abstract: Syntheses with N‐Trimethylsilylheteroarylium Salts: Reactions with Aldehydes, Ketones, and Carboxylic Acids. Comparison of Reactivity with Analogous N‐Acylheteroarylium Salts.(1988)