Synthesis Of Imidazo[1,2-a]pyridin-5-one Derivatives with a β-Hydroxyethyl Group on the Nitrogen Atom
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919708006041
Reference16 articles.
1. Heterocyclic β‐Enamino Esters, 33. Addition and Cyclization Reaction of 3‐(2‐Imidazolidinylidene)‐and 3‐(Hexahydro‐2‐pyrimidinylidene)‐2(3 H )‐furanones with Hydrochloric Acid, Halogens, and Methyl Propiolate
2. Heterocyclic β‐Enamino Esters, 34. New Types of Spiro Compounds by Addition and Cyclization Reactions of 3‐(2‐Imidazolidinylidene)‐ and 3‐(Tetrahydro‐2(1 H )‐pyrimidinylidene)dihydro‐2(3 H ‐furanones with Methyl Acrylate and Dimethyl Acetylenedicarboxylate
3. Synthesis of ketene aminals with an imidazolidine ring by condensation of 4,5‐dihydro‐2‐(methylithio)‐1 H ‐imidazoles with active methylene compounds and some addition and cyclocondensation reactions
4. Synthesis of Imidazo[1,2-a]pyridine and Pyrido[1,2-a]pyrimidine Derivatives by the Addition and Cyclocondensation Reactions of Ketenaminals Containing Imidazolidine or Hexahydropyrimidine Ring with Esters of a,b-Unsaturated Acids
5. A facile ring cleavage of cyclic ketones. Synthesis of 9-(alkoxycarbonylalkyl)pyrido[1,2-a]pyrimidines
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