An Unexpected Pyrimidine Ring Transformations in the Reaction of 4-aryl-5-nitro-6-bromomethylpyrimidin-2(1H)-ones with Anilines
Author:
Affiliation:
1. Priaxon AG; Gmunder Str. 37-37A D-81379 Munich Germany
2. Nanoscape AG; Am Klopferspitz 19 D-81252 Planegg Germany
3. Department Chemie; Ludwig-Maximilians-Universität München; Butenandtstraße 5-13, Haus F 81377 Munich Germany
Publisher
Wiley
Subject
Organic Chemistry
Reference25 articles.
1. 100 years of the biginelli dihydropyrimidine synthesis
2. 4-Aryldihydropyrimidines via the Biginelli Condensation: Aza-Analogs of Nifedipine-Type Calcium Channel Modulators
3. Biologically active dihydropyrimidones of the Biginelli-type — a literature survey
4. Recent Advances in the Biginelli Dihydropyrimidine Synthesis. New Tricks from an Old Dog
5. Synthesis of Dihydropyrimidinones and Thiones by Multicomponent Reactions: Strategies Beyond the Classical Biginelli Reaction
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1. Bicyclic 5–6 Systems: Other Four Heteroatoms 2:2;Comprehensive Heterocyclic Chemistry IV;2022
2. Metal-free synthesis and characterization of 1,3-Bis(heteroaryl)benzenes followed by the photophysical studies using ultraviolet–visible and fluorescence spectroscopy;Journal of Molecular Structure;2020-11
3. Transformations of Di- and Tetrahydropyrimidine Derivatives into Condensed Heterocycles with Retention of their Partially Saturated Structure;Journal of Heterocyclic Chemistry;2017-03-23
4. ChemInform Abstract: An Unexpected Pyrimidine Ring Transformations in the Reaction of 4-Aryl-5-nitro-6-bromomethylpyrimidin-2(1H)-ones with Anilines.;ChemInform;2016-07
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