An alternative synthesis of pyrimido[4,5-b]quinoline-4-ones via metal-free amination in water and Vilsmeier–Haack cyclization
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference68 articles.
1. Vilsmeier-Haack reaction with glutarimides. Synthesis of 2,6-dichloro-1,4-dihydropyridine-3,5-dicarboxaldehydes
2. Synthesis, antimicrobial activities and cytogenetic studies of newer diazepino quinoline derivatives via Vilsmeier–Haack reaction
3. Polyfunctional imidazoles: I. Synthesis of 1-substituted 4-chloro-1H-imidazole-5-carbaldehydes by Vilsmeier-Haack reaction
4. One-Pot Synthesis of Heterocyclic β-Chlorovinyl Aldehydes Using Vilsmeier Reagent
5. Reaction of α-Oxoketene-N,S-arylaminoacetals with Vilsmeier Reagents: An Efficient Route to Highly Functionalized Quinolines and Their Benzo/Hetero-Fused Analogues
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1. Synthetic approaches for quinoline heterocycles fused at face b: A review;Synthetic Communications;2024-08-19
2. Synthetic methodology of pyrimido[4,5‐b]quinoline derivatives;Journal of Heterocyclic Chemistry;2024-04-03
3. Synthesis, in silico screening, and biological evaluation of novel pyridine congeners as anti‐epileptic agents targeting AMPA (α‐amino‐3‐hydroxy‐5‐methylisoxazole) receptors;Chemical Biology & Drug Design;2024-03
4. Synthesis of pyrimido[4,5- b ]quinolindiones and formylation: ultrasonically assisted reactions;Royal Society Open Science;2024-03
5. Review: synthesis and anticancer activity of pyrimido[4,5-b]quinolines in the last twenty years;Chemical Papers;2024-02-12
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