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Medicinal chemistry perspective of pyrido[2,3-d]pyrimidines as anticancer agents
RSC Advances,
2023
DOI:10.1039/D3RA00056G
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[2]
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Quantitative phase analysis of commercial ammonium phosphates by PXRD for application in biological systems
Powder Diffraction,
2023
DOI:10.1017/S0885715623000167
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[3]
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One-Pot Multicomponent Reactions in Deep Eutectic Solvents
Current Organic Chemistry,
2023
DOI:10.2174/1385272827666230427101210
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Four-Component Condensation of Ethyl Acetoacetate, Phenylglyoxal Hydrate, Barbituric Acid, and Primary Amines
Russian Journal of Organic Chemistry,
2023
DOI:10.1134/S1070428023080067
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Insight into the cation-regulated mechanism for the hydration of propargyl alcohols catalyzed by [Bu4P+][Im−]
Journal of Molecular Liquids,
2022
DOI:10.1016/j.molliq.2022.120021
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[6]
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A greener approach for the synthesis of pyrido[2,3‐
d
]pyrimidine derivatives in glycerol under microwave heating
Journal of Heterocyclic Chemistry,
2022
DOI:10.1002/jhet.4483
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[7]
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Insight into the cation-regulated mechanism for the hydration of propargyl alcohols catalyzed by [Bu4P+][Im−]
Journal of Molecular Liquids,
2022
DOI:10.1016/j.molliq.2022.120021
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Agar-entrapped sulfonated DABCO: Agelly acidic catalyst for the acceleration of one-pot synthesis of 1,2,4-triazoloquinazolinone and some pyrimidine derivatives
Journal of Molecular Structure,
2021
DOI:10.1016/j.molstruc.2020.129336
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[9]
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Agar-entrapped sulfonated DABCO: Agelly acidic catalyst for the acceleration of one-pot synthesis of 1,2,4-triazoloquinazolinone and some pyrimidine derivatives
Journal of Molecular Structure,
2021
DOI:10.1016/j.molstruc.2020.129336
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[10]
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Synthesis of pyrano[2,3‐d]pyrimidines and pyrido[2,3‐d]pyrimidines in the magnetized deionized water based on UV–visible study
Journal of the Iranian Chemical Society,
2021
DOI:10.1007/s13738-020-02073-z
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[11]
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An overview on synthetic and pharmaceutical prospective of pyrido[2,3‐d]pyrimidines scaffold
Chemical Biology & Drug Design,
2021
DOI:10.1111/cbdd.13800
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[12]
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Synthesis of heterocyclic compounds via Michael and Hantzsch reactions
Journal of Heterocyclic Chemistry,
2020
DOI:10.1002/jhet.3883
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[13]
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A novel amphipathic low-melting complex salt: An efficient homogeneous catalyst for synthesis of pyran-annulated heterocyclic scaffolds and pyrido[2,3-d]pyrimidines
Journal of Molecular Liquids,
2020
DOI:10.1016/j.molliq.2020.112989
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[14]
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An overview on synthetic and pharmaceutical prospective of pyrido[2,3‐
d
]pyrimidines scaffold
Chemical Biology & Drug Design,
2020
DOI:10.1111/cbdd.13800
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[15]
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An expeditious one-pot synthesis of pyrido[2,3-d]pyrimidines using Fe3O4–ZnO–NH2–PW12O40 nanocatalyst
Journal of Chemical Research,
2019
DOI:10.1177/1747519819856978
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[16]
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An Efficient Protocol for the Synthesis of Pyrido[2,3‐
d
]pyrimidines in Glycerol–Water Medium: Assessment by Green Chemistry Metrics
Macromolecular Symposia,
2019
DOI:10.1002/masy.201800202
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[17]
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Aqueous Media Preparation of Pyrido[d]pyrimidines Over Calcined TiO2- SiO2 Nanocomposite as an Efficient Catalyst at Ambient Temperature
Letters in Organic Chemistry,
2019
DOI:10.2174/1570178616666181210102146
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[18]
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Expedient multicomponent synthesis of a small library of some novel highly substituted pyrido[2,3-d]pyrimidine derivatives mediated and promoted by deep eutectic solvent and in vitro and quantum mechanical study of their antibacterial and antifungal activities
Molecular Diversity,
2019
DOI:10.1007/s11030-018-9859-7
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[19]
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Application of 1‐methyl imidazole‐based ionic liquid‐stabilized silica‐coated Fe3O4 as a novel modified magnetic nanocatalyst for the synthesis of pyrano[2,3‐d]pyrimidines
Journal of the Chinese Chemical Society,
2019
DOI:10.1002/jccs.201800171
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[20]
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An Efficient Protocol for the Synthesis of Pyrido[2,3‐d]pyrimidines in Glycerol–Water Medium: Assessment by Green Chemistry Metrics
Macromolecular Symposia,
2019
DOI:10.1002/masy.201800202
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[21]
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Isatin‐SO3H coated on amino propyl modified magnetic nanoparticles (Fe3O4@APTES@isatin‐SO3H) as a recyclable magnetic nanoparticle for the simple and rapid synthesis of pyrano[2,3‐d] pyrimidines derivatives
Applied Organometallic Chemistry,
2019
DOI:10.1002/aoc.4602
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[22]
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Eco-friendly synthesis of pyrimidines and its derivatives: A review on broad spectrum bioactive moiety with huge therapeutic profile
Synthetic Communications,
2018
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[23]
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DABCO-based ionic liquids: introduction of two metal-free catalysts for one-pot synthesis of 1,2,4-triazolo[4,3-a]pyrimidines and pyrido[2,3-d]pyrimidines
New Journal of Chemistry,
2018
DOI:10.1039/C8NJ01455H
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[24]
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Antibacterial activity of synthetic pyrido[2,3-d]pyrimidines armed with nitrile groups: POM analysis and identification of pharmacophore sites of nitriles as important pro-drugs
New Journal of Chemistry,
2018
DOI:10.1039/C8NJ02081G
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[25]
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Application of 1-methyl imidazole-based ionic liquid-stabilized silica-coated Fe3
O4
as a novel modified magnetic nanocatalyst for the synthesis of pyrano[2,3-d]pyrimidines
Journal of the Chinese Chemical Society,
2018
DOI:10.1002/jccs.201800171
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[26]
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Isatin-SO3
H coated on amino propyl modified magnetic nanoparticles (Fe3
O4
@APTES@isatin-SO3
H) as a recyclable magnetic nanoparticle for the simple and rapid synthesis of pyrano[2,3-d] pyrimidines derivatives
Applied Organometallic Chemistry,
2018
DOI:10.1002/aoc.4602
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[27]
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Green Microwave-assisted Multicomponent Route to the Formation of 5,8-Dihydropyrido[2,3-d]pyrimidine Skeleton in Aqueous Media
Journal of Heterocyclic Chemistry,
2017
DOI:10.1002/jhet.2586
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[28]
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Recent Developments in the MCRs Synthesis of Pyridopyrimidines and Spiro-Pyridopyrimidines
Journal of Heterocyclic Chemistry,
2017
DOI:10.1002/jhet.2783
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[29]
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A green one-pot three-component cascade reaction: the synthesis of 2-amino-5,8-dihydro-3H-pyrido[2,3-D]pyrimidin-4-ones in aqueous medium
Molecular Diversity,
2017
DOI:10.1007/s11030-016-9712-9
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[30]
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Unexpected straightforward formation of trifluoromethylated pyrido[2,3- d ]pyrimidine derivatives via one-pot, MCRs
Journal of Fluorine Chemistry,
2017
DOI:10.1016/j.jfluchem.2017.06.016
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[31]
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Recent Developments in the MCRs Synthesis of Pyridopyrimidines and Spiro‐Pyridopyrimidines
Journal of Heterocyclic Chemistry,
2017
DOI:10.1002/jhet.2783
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[32]
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Green Microwave‐assisted Multicomponent Route to the Formation of 5,8‐Dihydropyrido[2,3‐d]pyrimidine Skeleton in Aqueous Media
Journal of Heterocyclic Chemistry,
2017
DOI:10.1002/jhet.2586
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[33]
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Synthesis of Novel 15-aryl-2,3,4,15-tetrahydrochromeno[2′,3′:4,5] Pyrimido[6,1-b]Quinazoline-1,9-diones
Journal of Chemical Research,
2016
DOI:10.3184/174751916X14527702465295
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[34]
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A catalyst free, multicomponent-tandem, facile synthesis of pyrido[2,3-d]pyrimidines using glycerol as a recyclable promoting medium
New J. Chem.,
2016
DOI:10.1039/C5NJ01938A
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[35]
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Efficient one-pot synthesis of new fused pyridines and bis-pyridines catalyzed by triazine diphosphonium hydrogen sulfate ionic liquid supported on functionalized nano-silica
Tetrahedron Letters,
2016
DOI:10.1016/j.tetlet.2016.04.053
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[36]
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Molecular and supramolecular chemistry of rosette nanotubes
RSC Adv.,
2016
DOI:10.1039/C6RA16315G
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[37]
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An efficient one pot three component synthesis of fused pyridines via electrochemical approach
Tetrahedron Letters,
2016
DOI:10.1016/j.tetlet.2016.10.111
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[38]
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Transition metal-free one-pot synthesis of nitrogen-containing heterocycles
Molecular Diversity,
2016
DOI:10.1007/s11030-015-9596-0
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[39]
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Polyethylene glycol-bonded 1,8-diazabicyclo[5.4.0]undec-7-ene (PEG–DBU) as a surfactant-combined base catalyst for the application of nucleosides as reagents in multi-component syntheses of 8-substituted pyrido[2,3-d]pyrimidine-6-carbonitriles in water
Green Chem.,
2015
DOI:10.1039/C5GC01448D
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[40]
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Efficient and Easy One-Pot Synthesis of New 3,5-Dioxo-thiazolo[2,3-a] pyrimidine-6-carbonitrile and 4,6-Dioxo-pyrimido[2,1-b][1,3]thiazine-7-carbonitrile Derivatives
Journal of Heterocyclic Chemistry,
2015
DOI:10.1002/jhet.2085
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[41]
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Eco-friendly synthesis of pyrano[2,3-d]pyrimidinone derivatives catalyzed by a novel nanocatalyst of ZnO-supported copper oxide in water
Research on Chemical Intermediates,
2015
DOI:10.1007/s11164-014-1894-0
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[42]
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Efficient one-pot synthesis of pyrido[2,3-d]pyrimidines catalyzed by nanocrystalline MgO in water
International Nano Letters,
2015
DOI:10.1007/s40089-015-0145-8
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[43]
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Synthesis and properties of derivatives of pyrimidin-5-ylpropanoic acids and 8-aryl-4-methyl- and 4,6-dimethyl-2-phenyl-5,6,7,8-tetrahydropyrido-[2,3-d]pyrimidin-7-ones
Russian Journal of Organic Chemistry,
2015
DOI:10.1134/S1070428015050218
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[44]
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Efficient and Easy One‐Pot Synthesis of New 3,5‐Dioxo‐thiazolo[2,3‐a] pyrimidine‐6‐carbonitrile and 4,6‐Dioxo‐pyrimido[2,1‐b][1,3]thiazine‐7‐carbonitrile Derivatives
Journal of Heterocyclic Chemistry,
2015
DOI:10.1002/jhet.2085
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[45]
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Synthesis of fused pyridines in the presence of thiamine hydrochloride as an efficient and reusable catalyst in aqueous conditions
New Journal of Chemistry,
2013
DOI:10.1039/c3nj00711a
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[46]
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Facile synthesis of pyridopyrimidine and coumarin fused pyridine libraries over a Lewis base-surfactant-combined catalyst TEOA in aqueous medium
RSC Advances,
2013
DOI:10.1039/c3ra23254a
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