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Condensationsprodukte aus Aldehydammoniak und ketonartigen Verbindungen

https://doi.org/10.1002/cber.18810140214

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inferred← citeshttps://doi.org/10.1007/s10989-015-9460-1openalex-snapshot

1,4-Dihydropyridine Cationic Peptidomimetics with Antibacterial Activity

inferred← citeshttps://doi.org/10.1007/s11030-015-9594-2openalex-snapshot

Recent developments in utility of green multi-component reactions for the efficient synthesis of polysubstituted pyrans, thiopyrans, pyridines, and pyrazoles

inferred← citeshttps://doi.org/10.1007/s11030-020-10109-yopenalex-snapshot

Urease: a highly efficient biocatalyst for synthesis of polyhydroquinolines and polyhydroacridines from the ammonia formed in situ

inferred← citeshttps://doi.org/10.1007/s11164-016-2579-7openalex-snapshot

Chitosan: a sustainable, reusable and biodegradable organocatalyst for green synthesis of 1,4-dihydropyridine derivatives under solvent-free condition

inferred← citeshttps://doi.org/10.1007/s11164-023-05201-5openalex-snapshot

Covalent immobilization of di-cationic DABCO ionic liquid over graphene oxide as an efficient and recyclable nanocomposite for the synthesis of Knoevenagel and Hantzsch reactions

inferred← citeshttps://doi.org/10.1007/s11705-022-2150-6openalex-snapshot

Sustainable functionalization and modification of materials via multicomponent reactions in water

inferred← citeshttps://doi.org/10.1007/s12039-015-0983-yopenalex-snapshot

One-pot synthesis of N-aryl 1,4-dihydropyridine derivatives and their biological activities

inferred← citeshttps://doi.org/10.1007/s12039-020-01850-wopenalex-snapshot

Sulfated polyborate as an eco-compatible solid acid catalyst for efficient and facile solvent-free synthesis of polyhydroquinolines

inferred← citeshttps://doi.org/10.1007/s13738-011-0010-2openalex-snapshot

Highly efficient methodology for aromatization of 1, 4-dihydropyridines using silica-supported transition metal nitrates under infra-red radiations

inferred← citeshttps://doi.org/10.1007/s13738-016-0964-1openalex-snapshot

Nanometasilica disulfuric acid (NMSDSA) and nanometasilica monosulfuric acid sodium salt (NMSMSA) as two novel nanostructured catalysts: applications in the synthesis of Biginelli-type, polyhydroquinoline and 2,3-dihydroquinazolin-4(1H)-one derivatives

inferred← citeshttps://doi.org/10.1007/s41061-016-0032-4openalex-snapshot

Organocatalytic Transfer Hydrogenation and Hydrosilylation Reactions

inferred← citeshttps://doi.org/10.1007/s41061-023-00440-xopenalex-snapshot

Construction of 1,4-Dihydropyridines: The Evolution of C4 Source

inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00628-5openalex-snapshot

6.25 Reduction: Asymmetric Transfer Hydrogenation with Hantzsch Esters

inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14679-7openalex-snapshot

Chemistry and Chemical Biology of Thiopeptide Natural Products

inferred← citeshttps://doi.org/10.1016/b978-0-12-800070-0.00019-0openalex-snapshot

Microwave-Induced Synthesis of Heterocycles of Medicinal Interests

inferred← citeshttps://doi.org/10.1016/b978-0-12-817467-8.00002-5openalex-snapshot

5-(Hydroxymethyl)furfural and 5-(glucosyloxymethyl)furfural in multicomponent reactions

inferred← citeshttps://doi.org/10.1016/b978-0-12-818584-1.00001-xopenalex-snapshot

Introduction

inferred← citeshttps://doi.org/10.1016/b978-0-12-818584-1.00002-1openalex-snapshot

Direct synthesis of heterocycles via MCRs, using a name reaction

inferred← citeshttps://doi.org/10.1016/b978-0-12-818584-1.00003-3openalex-snapshot

Synthesis of heterocycles via MCRs, using a name reaction in combination with another reaction

inferred← citeshttps://doi.org/10.1016/b978-0-12-819210-8.00002-3openalex-snapshot

Six-Membered Heterocycles

inferred← citeshttps://doi.org/10.1016/b978-0-12-819848-3.00003-7openalex-snapshot

Microwave-assisted multicomponent reactions

inferred← citeshttps://doi.org/10.1016/b978-0-12-820586-0.00004-2openalex-snapshot

Microwave-assisted multicomponent reactions as a green synthetic approach to heterocycles: special reference to Hantzsch, Biginelli, and Groebke–Blackburn–Bienayme reactions

inferred← citeshttps://doi.org/10.1016/b978-0-12-820586-0.00009-1openalex-snapshot

Microwave-assisted synthesis of medicinally privileged heterocycles

inferred← citeshttps://doi.org/10.1016/b978-0-323-91221-1.00014-2openalex-snapshot

Synthetic strategies of functionalized pyridines and their therapeutic potential as multifunctional anti-Alzheimer's agents

inferred← citeshttps://doi.org/10.1016/b978-0-323-95921-6.00005-6openalex-snapshot

Nano-catalyzed synthesis of pyranopyrazole and pyridine scaffolds

inferred← citeshttps://doi.org/10.1016/b978-0-443-36542-3.00014-1openalex-snapshot

Chemical synthesis as design and construction of molecular architectures: a brief history

inferred← citeshttps://doi.org/10.1016/bs.aihch.2016.04.007openalex-snapshot

Multicomponent Syntheses of Heterocycles Initiated by Catalytic Generation of Ynones and Ynediones

inferred← citeshttps://doi.org/10.1016/bs.aihch.2023.01.001openalex-snapshot

Recent developments in the synthesis of 4-, 5-, 6- and 7-azaindoles

inferred← citeshttps://doi.org/10.1016/bs.aihch.2023.04.001openalex-snapshot

Recent developments in the Hantzsch synthesis of dihydropyridines

inferred← citeshttps://doi.org/10.1016/j.arabjc.2021.103026openalex-snapshot

Synthesis and characterization of [Fe3O4@CQDs@Si(CH2)3NH2@CC@EDA@SO3H]+Cl− and Fe3O4@CQDs@Si(CH2)3NH2@CC@EDA@Cu nanocatalyts and their application in the synthesis of 5-amino-1,3-diphenyl-1H-pyrazole-4-carbonitrile and 1-(morpholino(phenyl)methyl)naphthalen-2-ol derivatives

inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.104514openalex-snapshot

1-Benzamido-1,4-dihydropyridine derivatives as anticancer agents: in vitro and in vivo assays

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105054openalex-snapshot

Revisiting ageless antiques; synthesis, biological evaluation, docking simulation and mechanistic insights of 1,4-Dihydropyridines as anticancer agents

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109393openalex-snapshot

Cytotoxicity, apoptosis, molecular docking, and molecular dynamics study of novel compounds of Sulfamide derivatives coupled with DHP scaffolds as potent inhibitors of the MCF-7, A549, SKOV-3, and EA. yh926 carcinoma cells

inferred← citeshttps://doi.org/10.1016/j.bmc.2014.07.044openalex-snapshot

Design, synthesis and evaluation of 2-aminothiazole derivatives as sphingosine kinase inhibitors

inferred← citeshttps://doi.org/10.1016/j.bmc.2020.115734openalex-snapshot

Design and synthesis of novel methoxypyridine-derived gamma-secretase modulators

inferred← citeshttps://doi.org/10.1016/j.bmc.2020.115816openalex-snapshot

Syntheses and anti-HIV and human cluster of differentiation 4 (CD4) down-modulating potencies of pyridine-fused cyclotriazadisulfonamide (CADA) compounds

inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.04.002openalex-snapshot

Oxidative aromatization of Hantzsch 1,4-dihydropyridines in the presence of mixed-addenda vanadomolybdophosphate heteropolyacid, H6PMo9V3O40

inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.04.024openalex-snapshot

Novel pyridopyrimidine derivatives as inhibitors of stable toxin a (STa) induced cGMP synthesis

inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.07.011openalex-snapshot

Design and synthesis of aminothiazole modulators of the gamma-secretase enzyme

inferred← citeshttps://doi.org/10.1016/j.catcom.2008.12.005openalex-snapshot

Oxidative aromatization of Hantzsch 1,4-dihydropyridines in the presence of a catalytic amount of Mn(pbdo)2Cl2/MCM-41 or Mn(pbdo)2Cl2/Al-MCM-41 as reusable and green catalysts

inferred← citeshttps://doi.org/10.1016/j.catcom.2015.09.006openalex-snapshot

Urease: A highly biocompatible catalyst for switchable Biginelli reaction and synthesis of 1,4-dihydropyridines from the in situ formed ammonia

inferred← citeshttps://doi.org/10.1016/j.cattod.2017.05.038openalex-snapshot

V 2 O 5 /ZrO 2 as an efficient reusable catalyst for the facile, green, one-pot synthesis of novel functionalized 1,4-dihydropyridine derivatives

inferred← citeshttps://doi.org/10.1016/j.cep.2025.110205openalex-snapshot

Blue LED photolytic method for the synthesis of 1,4-dihydropyridine derivatives from benzo [b]thiophene-2-carbaldehyde

inferred← citeshttps://doi.org/10.1016/j.cplett.2008.07.070openalex-snapshot

35Cl-NQR and DFT study of electronic structure of amlodipine and felodipine vascular-selective drugs from the dihydropyridine Ca++ antagonists group

inferred← citeshttps://doi.org/10.1016/j.cplett.2008.08.026openalex-snapshot

13C CP MAS NMR and DFT study of vascular-selective drugs felodipine and amlodipine

inferred← citeshttps://doi.org/10.1016/j.crci.2014.08.006openalex-snapshot

Solvent-free multicomponent synthesis of 2-arylpyridines using p-sulfonic acid calix[6]arene as a reusable catalyst

inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.11.007openalex-snapshot

Design, synthesis and investigation on the structure–activity relationships of N-substituted 2-aminothiazole derivatives as antitubercular agents

inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117526openalex-snapshot

The Liebeskind–Srogl cross-coupling reaction towards the synthesis of biologically active compounds

inferred← citeshttps://doi.org/10.1016/j.foodchem.2024.138577openalex-snapshot

High performance liquid chromatography coupled with post – Column derivatization methods in food analysis: Chemistries and applications in the last two decades

inferred← citeshttps://doi.org/10.1016/j.ica.2016.01.019openalex-snapshot

Synthesis and (spectro)electrochemical investigations of coordinatively-saturated (cyclopentadienyl)ruthenium–Hantzsch pyridinium/dihydropyridine conjugates

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.137832openalex-snapshot

Core-shell structured magnetite carboxymethyl cellulose for cervical cancer treatment by maintaining methotrexate serum concentration

inferred← citeshttps://doi.org/10.1016/j.isci.2019.100754openalex-snapshot

High-Throughput Preparation of Antibacterial Polymers from Natural Product Derivatives via the Hantzsch Reaction

inferred← citeshttps://doi.org/10.1016/j.jcis.2017.03.084openalex-snapshot

Alkyl-imidazolium based organosilica supported Fe/porphyrin complex: As novel, highly efficient and reusable catalyst for the unsymmetrical Hantzsch reaction

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.10.017openalex-snapshot

New nucleophilic rearrangement in the mechanism of the three-component domino cyclisation affording fluoroalkylated (pyrrolo)quinazolines

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121232openalex-snapshot

Synthesis, characterization and application of Copper/Schiff-base complex immobilized on KIT-6-NH2 magnetic nanoparticles for the synthesis of dihydropyridines

inferred← citeshttps://doi.org/10.1016/j.jscs.2012.08.003openalex-snapshot

Design and synthesis of novel 4-substituted 1,4-dihydropyridine derivatives as hypotensive agents

inferred← citeshttps://doi.org/10.1016/j.jtice.2025.106249openalex-snapshot

Sustainable, one-pot multicomponent synthesis of 1,4-dihydropyridines, benzylidene malononitriles and tetrahydrobenzo[b]pyrans using copper nanoparticles: Exploration of green chemistry metrics and antioxidant potential

inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112819openalex-snapshot

Photoinduced cyclization of aryl ynones with 4-alkyl-DHPs for the divergent synthesis of indenones, thioflavones and spiro[5.5]trienones

inferred← citeshttps://doi.org/10.1016/j.mencom.2017.01.031openalex-snapshot

Microwave-promoted reaction of N-(alk-1-enyl)chloroacetamides with sodium azide unexpectedly yields 1H-imidazol-5(4H)-ones

inferred← citeshttps://doi.org/10.1016/j.molcata.2010.11.012openalex-snapshot

Cellulose sulfuric acid catalyzed multicomponent reaction for efficient synthesis of 1,4-dihydropyridines via unsymmetrical Hantzsch reaction in aqueous media

inferred← citeshttps://doi.org/10.1016/j.molcata.2014.04.025openalex-snapshot

Silica functionalized propyl sulfonic acid (SiO2-Pr-SO3H): An efficient catalyst in organic reactions

inferred← citeshttps://doi.org/10.1016/j.molliq.2012.10.045openalex-snapshot

Synthesis, characterization and application of ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient catalyst for the preparation of hexahydroquinolines

inferred← citeshttps://doi.org/10.1016/j.molliq.2015.01.013openalex-snapshot

Effective preparation of hexahydroquinolines under ambient and solvent-free conditions

inferred← citeshttps://doi.org/10.1016/j.molliq.2018.04.125openalex-snapshot

Anchoring high density sulfonic acid based ionic liquid on the magnetic nano-magnetite (Fe3O4), application to the synthesis of hexahydroquinoline derivatives

inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131890openalex-snapshot

Synthesis, single crystal, characterization and computational study of 2-amino-N-cyclopropyl-5-ethyl-thiophene-3-carboxamide

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