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Sequential Amination/Annulation/Aromatization Reaction of Carbonyl Compounds and Propargylamine: A New One-Pot Approach to Functionalized Pyridines

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jhet.5570030321openalex-snapshot
5α‐androstano [3,2‐b]pyridines, 5α‐androstano[17,16‐b]pyridines and androst‐4 and 5‐eno[17,16‐b]pyridines
inferredcites →https://doi.org/10.1016/s0022-328x(00)83849-8openalex-snapshot
Specific and selective reduction of aromatic nitrogen heterocycles with the bis-pyridine complexes of bis(1,4-dihydro-1-pyridyl)zinc and bis(1,4-dihydro-1-pyridyl)magnesium
inferredcites →https://doi.org/10.1016/s0022-328x(00)92682-2openalex-snapshot
Cyclometallation. Palladium 2-arylpyridine complexes
inferredcites →https://doi.org/10.1016/s0040-4039(00)01666-xopenalex-snapshot
Sequential alkylation/transition metal catalysed annulation reactions of 1,3-dicarbonyl compounds with propargyl bromide
inferredcites →https://doi.org/10.1016/s0040-4039(02)01975-5openalex-snapshot
A new one-step synthesis of pyridines under microwave-assisted conditions
inferredcites →https://doi.org/10.1016/s0040-4039(99)01351-9openalex-snapshot
One-pot asymmetric synthesis of tert-butanesulfinyl-protected amines from ketones by the in situ reduction of tert-butanesulfinyl ketimines
inferredcites →https://doi.org/10.1016/s0960-894x(02)00943-5openalex-snapshot
Pharmacophore-Based discovery of substituted pyridines as novel dopamine transporter inhibitors
inferredcites →https://doi.org/10.1021/cc020067dopenalex-snapshot
A Facile Solution Phase Combinatorial Synthesis of Tetrasubstituted Pyridines Using the Bohlmann-Rahtz Heteroannulation Reaction
inferredcites →https://doi.org/10.1021/jm020311fopenalex-snapshot
Metabolism-Directed Optimization of 3-Aminopyrazinone Acetamide Thrombin Inhibitors. Development of an Orally Bioavailable Series Containing P1 and P3 Pyridines
inferredcites →https://doi.org/10.1021/jo00217a050openalex-snapshot
Acidity measurements on pyridines in tetrahydrofuran using lithiated silylamines
inferredcites →https://doi.org/10.1021/jo00217a051openalex-snapshot
An apparent, deep-seated, carbonium-mediated sesquiterpene rearrangement
inferredcites →https://doi.org/10.1021/jo01047a047openalex-snapshot
The Preparation of Tetrahydropyridines from Enamines and Imines1
inferredcites →https://doi.org/10.1021/jo991609popenalex-snapshot
Enantiospecific Synthesis of Annulated Nicotine Analogues from d - and l -Glutamic Acid. Pyridotropanes
inferredcites →https://doi.org/10.1021/om0009987openalex-snapshot
Transition Metal-Catalyzed Addition of Amines to Acrylic Acid Derivatives. A High-Throughput Method for Evaluating Hydroamination of Primary and Secondary Alkylamines
inferredcites →https://doi.org/10.1039/b210165copenalex-snapshot
Gold catalysis in the reactions of 1,3-dicarbonyls with nucleophiles
inferredcites →https://doi.org/10.1248/bpb.26.182openalex-snapshot
Pharmacological Evaluation of Some New 2-Substituted Pyridine Derivatives.
inferredcites →https://doi.org/10.1248/cpb.51.162openalex-snapshot
Pharmacological Evaluation of Some New 6-Amino/Methyl Pyridine Derivatives.
inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.16.186openalex-snapshot
Progress in Heterocyclic Chemistry

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4733424openalex-extracted
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inferred← citeshttps://doi.org/10.1002/047084289x.rs108.pub2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/0470862106.ia459openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/0471264180.or092.01openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470682531.pat0807openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos09351.pub2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos09351.pub3openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos09351.pub4openalex-snapshot
Sodium Tetrachloroaurate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos09351.pub5openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos09351.pub6openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118356654.ch4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118651421.ch4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0359openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527621262.ch6openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527623778.ch8openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527646869.ch4openalex-snapshot
Gold‐Catalyzed Reactions of Propargyl Esters, Propargyl Alcohols, and Related Compounds
inferred← citeshttps://doi.org/10.1002/9783527826186.ch4openalex-snapshot
Propargylamines: Recent Advances in Asymmetric Synthesis and Use as Chemical Tools in Organic Chemistry
inferred← citeshttps://doi.org/10.1002/adsc.201000292openalex-snapshot
Synthesis of Substituted 1,2‐Dihydropyridines from Propargyl Vinyl Ethers and Allenic Vinyl Ethers by Gold‐Catalyzed Claisen Rearrangement and 6π‐Aza‐electrocyclization
inferred← citeshttps://doi.org/10.1002/adsc.201500520openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201500685openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201600412openalex-snapshot
Substrate Control in the Gold(I)‐Catalyzed Cyclization of β‐Propargylamino Acrylic Esters and Further Transformations of the Resultant Dihydropyridines
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inferred← citeshttps://doi.org/10.1002/ajoc.202000444openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.202200480openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200502735openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200600408openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200602454openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201100044openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201208603openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200502735openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200600408openalex-snapshot
In(OTf)3‐Catalyzed Tandem Nucleophilic Addition and Cyclization of ortho‐Alkynylarylaldimines to 1,2‐Dihydroisoquinolines
inferred← citeshttps://doi.org/10.1002/anie.200602454openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201100044openalex-snapshot
Efficient Gold(I)‐Catalyzed Direct Intramolecular Hydroalkylation of Unactivated Alkenes with α‐Ketones
inferred← citeshttps://doi.org/10.1002/anie.201208603openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ceat.200900368openalex-snapshot
Heterogeneous Catalyzed Pyridine Synthesis using Montmorillionite and Nanoparticle‐Impregnated Alumina in a Continuous Micro Flow System
inferred← citeshttps://doi.org/10.1002/chem.200400322openalex-snapshot
A New Color of the Synthetic Chameleon Methoxyallene: Synthesis of Trifluoromethyl‐Substituted Pyridinol Derivatives: An Unusual Reaction Mechanism, a Remarkable Crystal Packing, and First Palladium‐Catalyzed Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201002150openalex-snapshot
Mechanism of the Dehydrogenative Silylation of Alcohols Catalyzed by Cationic Gold Complexes: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1002/chem.202203992openalex-snapshot
Scaffold Remodelling of Diazaspirotricycles Enables Synthesis of Diverse sp 3 ‐Rich Compounds With Distinct Phenotypic Effects
inferred← citeshttps://doi.org/10.1002/chem.202300059openalex-snapshot
Facile One‐Pot Synthesis of Polysubstituted Pyridinium Salts by Annulation of Enamines with Alkynes
inferred← citeshttps://doi.org/10.1002/chin.200403124openalex-snapshot
Sequential Amination/Annulation/Aromatization Reaction of Carbonyl Compounds and Propargylamine: A New One‐Pot Approach to Functionalized Pyridines.
inferred← citeshttps://doi.org/10.1002/cmdc.202501102openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.200900039openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201100464openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201700086openalex-snapshot
Radical Cyclizations in the Synthesis of 3‐Methyl‐cis‐octahydroindol‐5‐ones
inferred← citeshttps://doi.org/10.1002/ejoc.201700559openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ijch.201300040openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ijch.201700045openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.380openalex-snapshot
Facile synthesis of 2,6‐diaryl‐4‐secondary aminonicotinonitriles and highly substituted unsymmetrical 2,2′‐bipyridines
inferred← citeshttps://doi.org/10.1002/jssc.200700062openalex-snapshot
Separation of pyridine derivatives from synthetic mixtures by pH‐zone‐refining counter‐current chromatography
inferred← citeshttps://doi.org/10.1002/nadc.20050530414openalex-snapshot
Carbenoide bei Enincyclisierungen
inferred← citeshttps://doi.org/10.1002/open.202200223openalex-snapshot
Propargyl Amines: Versatile Building Blocks in Post‐Ugi Transformations
inferred← citeshttps://doi.org/10.1002/slct.201801799openalex-snapshot
HKUST‐1‐Catalyzed Formation of C–C and C‐N Bonds: Rapid Assembly of Substituted Pyridines from Propargylamine and Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/slct.202403541openalex-snapshot
Gold(III)‐Catalyzed Cyclization/Skeletal Rearrangement Reaction for the Synthesis of 2,4,6‐Trisubstituted 3‐Hydroxypyridines
inferred← citeshttps://doi.org/10.1002/slct.202501880openalex-snapshot
Carbon‐Coated Copper Nanoparticles for Heterogeneous Catalytic Synthesis of Fused Pyridines: The Role of Cu and C Components
inferred← citeshttps://doi.org/10.1007/bf03215517openalex-snapshot
Homogeneous catalysis by gold
inferred← citeshttps://doi.org/10.1007/s10562-017-2102-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11164-019-03803-6openalex-snapshot
Heterogeneous bimetallic Au–Co nanoparticles as new efficient catalysts for the three-component coupling reactions of amines, alkynes and CH2Cl2
inferred← citeshttps://doi.org/10.1007/s13369-012-0313-3openalex-snapshot
Gold(III) Compounds for Homogeneous Catalysis: Preparation, Reaction Conditions, and Scope of Application
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00120-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-804034-8.00005-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-809379-5.00003-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00915-9openalex-snapshot
Bicyclic 6-6 Systems: Two Heteroatoms 1:1
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.08.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.aihch.2026.03.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2018.02.027openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2020.115442openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.02.030openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.128631openalex-snapshot
A unified “top-down” approach for the synthesis of diverse lead-like molecular scaffolds
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.03.033openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cej.2010.08.078openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.12.013openalex-snapshot
Sequential gold-catalyzed reactions of 1-phenylprop-2-yn-1-ol with 1,3-dicarbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.08.011openalex-snapshot
Tandem imination/annulation of γ- and δ-ketoalkynes in the presence of ammonia/amines
inferred← citeshttps://doi.org/10.1016/j.molcata.2016.09.008openalex-snapshot
Au-complex containing phosphino and imidazolyl moieties as a bi-functional catalyst for one-pot synthesis of pyridine derivatives
inferred← citeshttps://doi.org/10.1016/j.steroids.2007.06.002openalex-snapshot
One-pot synthesis of new A-ring fused steroidal pyridines
inferred← citeshttps://doi.org/10.1016/j.steroids.2013.01.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.steroids.2013.08.002openalex-snapshot
Palladium-catalyzed multi-component synthesis of steroidal A- and D-ring fused 5,6-disubstituted pyridines under microwave irradiation
inferred← citeshttps://doi.org/10.1016/j.steroids.2026.109796openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2008.05.082openalex-snapshot
Recent advances in syntheses of carbocycles and heterocycles via homogeneous gold catalysis. Part 2: Cyclizations and cycloadditions
inferred← citeshttps://doi.org/10.1016/j.tet.2009.12.012openalex-snapshot
Synthesis of substituted quinolines by the electrophilic cyclization of n-(2-alkynyl)anilines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.06.129openalex-snapshot
A mild access to γ- or δ-alkylidene lactones through gold catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.013openalex-snapshot
A convenient synthesis of pyrrolopyridines and 2-substituted indoles by gold-catalyzed cycloisomerization
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.07.115openalex-snapshot
Sequential alkylation/gold-catalyzed annulation reactions of anilines with propargylic bromide derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.012openalex-snapshot
Synthesis of [5,6]-fused pyridocoumarins through aza-Claisen rearrangement of 6-propargylaminocoumarins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.052openalex-snapshot
Domino four-component synthesis of novel cycloocta[b]pyridines
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00343openalex-snapshot
Synthesis and Reactivity of Propargylamines in Organic Chemistry
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c04601openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b01382openalex-snapshot
Discovery of BAY-298 and BAY-899: Tetrahydro-1,6-naphthyridine-Based, Potent, and Selective Antagonists of the Luteinizing Hormone Receptor Which Reduce Sex Hormone Levels in Vivo
inferred← citeshttps://doi.org/10.1021/acs.joc.0c03038openalex-snapshot
Cu-Catalyzed Pyridine Synthesis via Oxidative Annulation of Cyclic Ketones with Propargylamine
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02086openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.3c02976openalex-snapshot
[Au]-Catalyzed Cyclization of Propargyl-Tethered Ene-Amides: Substrate-Dependent Access to Tetrasubstituted Pyrroles, Aminophenols, and Dihydropyridines
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02981openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03236openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02132openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00251openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.7b00626openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr000436xopenalex-snapshot
Gold-Catalyzed Organic Reactions
inferred← citeshttps://doi.org/10.1021/cr020018nopenalex-snapshot
Concurrent Tandem Catalysis
inferred← citeshttps://doi.org/10.1021/cr050041jopenalex-snapshot
Coinage Metal-Assisted Synthesis of Heterocycles
inferred← citeshttps://doi.org/10.1021/cr0684319openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr068434lopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr068435dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr100307mopenalex-snapshot
Advances in the Chemistry of Tetrahydroquinolines
inferred← citeshttps://doi.org/10.1021/cr200164yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr300333uopenalex-snapshot
Transition Metal-Mediated Synthesis of Monocyclic Aromatic Heterocycles
inferred← citeshttps://doi.org/10.1021/cr500691kopenalex-snapshot
Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity
inferred← citeshttps://doi.org/10.1021/cr800420xopenalex-snapshot
Addition of Metal Enolate Derivatives to Unactivated Carbon−Carbon Multiple Bonds
inferred← citeshttps://doi.org/10.1021/ja0619758openalex-snapshot
Rhodium-Catalyzed Cycloisomerization of N -Propargyl Enamine Derivatives
inferred← citeshttps://doi.org/10.1021/ja311258eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo047793iopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo071014ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo071225wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo1006637openalex-snapshot
Azaanthraquinone Assembly from N-Propargylamino Quinone via a Au(I)-Catalyzed 6-endo-dig Cycloisomerization
inferred← citeshttps://doi.org/10.1021/jo801090hopenalex-snapshot
Me3SiCl-Promoted Three-Component Coupling Reaction of a Functionalized Enamine, an Acetal, and an Alkyne: An Unprecedented Approach to the Synthesis of Tetrasubstituted Pyridines via a [3 + 2 + 1] Intermolecular Cyclization
inferred← citeshttps://doi.org/10.1021/jo802043zopenalex-snapshot
Platinum-Catalyzed Cycloisomerization Reaction of 1,6-Enyne Coupling with Rearrangement of Propargylic Esters
inferred← citeshttps://doi.org/10.1021/ml300021sopenalex-snapshot
Discovery of BMS-846372, a Potent and Orally Active Human CGRP Receptor Antagonist for the Treatment of Migraine
inferred← citeshttps://doi.org/10.1021/ol062988topenalex-snapshot
Cobalt-Catalyzed Intramolecular [2 + 2 + 2] Cocyclotrimerization of Nitrilediynes: An Efficient Route to Tetra- and Pentacyclic Pyridine Derivatives
inferred← citeshttps://doi.org/10.1021/ol2015658openalex-snapshot
Gold Catalyzed Cyclization of Alkyne-Tethered Dihydropyrimidones
inferred← citeshttps://doi.org/10.1021/ol201655uopenalex-snapshot
Synthesis of 2,5-Dihydropyridine Derivatives by Gold-Catalyzed Reactions of β-Ketoesters and Propargylamines
inferred← citeshttps://doi.org/10.1021/ol5023596openalex-snapshot
Copper-Catalyzed Aerobic Synthesis of 2-Arylpyridines from Acetophenones and 1,3-Diaminopropane
inferred← citeshttps://doi.org/10.1021/ol800092popenalex-snapshot
Direct Carbocyclization of Aldehydes with Alkynes: Combining Gold Catalysis with Aminocatalysis
inferred← citeshttps://doi.org/10.1021/ol801589popenalex-snapshot
Pd-Catalyzed Efficient One-Pot Sequential Cross-Coupling Reactions of Aryl Dihalides
inferred← citeshttps://doi.org/10.1021/ol902716nopenalex-snapshot
Synthesis of Pyrroles by Gold(I)-Catalyzed Amino−Claisen Rearrangement of N-Propargyl Enaminone Derivatives
inferred← citeshttps://doi.org/10.1038/nchem.1798openalex-snapshot
Biogenetically inspired synthesis and skeletal diversification of indole alkaloids
inferred← citeshttps://doi.org/10.1039/b612008copenalex-snapshot
Molecular diversity through gold catalysis with alkynes
inferred← citeshttps://doi.org/10.1039/b925468dopenalex-snapshot
A three-component synthesis of β-alkoxy-β-keto-enamides—flexible precursors for 4-hydroxypyridine derivatives and their palladium-catalysed reactions
inferred← citeshttps://doi.org/10.1039/c004896hopenalex-snapshot
Azaanthraquinone assembly from N-propargylamino quinone via iodine-induced 6-endo-dig electrophilic cyclization
inferred← citeshttps://doi.org/10.1039/c0cc04383dopenalex-snapshot
A silver-promoted auto-tandem catalysis for the synthesis of multiply substituted tetrahydrocarbazoles
inferred← citeshttps://doi.org/10.1039/c1cc10780aopenalex-snapshot
Heterocycles from gold catalysis
inferred← citeshttps://doi.org/10.1039/c2ob26380gopenalex-snapshot
An alternative one-pot gold-catalyzed approach to the assembly of 11H-indolo[3,2-c]quinolines
inferred← citeshttps://doi.org/10.1039/c3md00282aopenalex-snapshot
Heterocycle-fused lupane triterpenoids inhibit Leishmania donovani amastigotes
inferred← citeshttps://doi.org/10.1039/c3ra46722hopenalex-snapshot
Efficient synthesis of isoquinolines and pyridines via copper(i)-catalyzed multi-component reaction
inferred← citeshttps://doi.org/10.1039/c4ob01019aopenalex-snapshot
One-pot synthesis of polysubstituted 3-acylpyrroles by cooperative catalysis
inferred← citeshttps://doi.org/10.1039/c4ra09153aopenalex-snapshot
Facile synthesis of 2-substituted quinolines and 3-alkynyl-2-aryl-2H-Indazole via SnCl 2 -mediated reductive cyclization
inferred← citeshttps://doi.org/10.1039/c6ra08720eopenalex-snapshot
New page to access pyridine derivatives: synthesis from N-propargylamines
inferred← citeshttps://doi.org/10.1039/c7qo00714kopenalex-snapshot
Photoredox-catalyzed cascade addition/cyclization of N -propargyl aromatic amines: access to 3-difluoroacetylated or 3-fluoroacetylated quinolines
inferred← citeshttps://doi.org/10.1039/c8md00077hopenalex-snapshot
Evaluation of A-ring fused pyridine d -modified androstane derivatives for antiproliferative and aldo–keto reductase 1C3 inhibitory activity
inferred← citeshttps://doi.org/10.1039/c9cc01097aopenalex-snapshot
A simple, tandem approach to the construction of pyridine derivatives under metal-free conditions: a one-step synthesis of the monoterpene natural product, (−)-actinidine
inferred← citeshttps://doi.org/10.1039/c9ra10885hopenalex-snapshot
Copper (triazole-5-yl)methanamine complexes onto MCM-41: the synthesis of pyridine-containing pseudopeptides through the 6- endo -dig cyclization of 1,5-enynes
inferred← citeshttps://doi.org/10.1039/d0cc00914hopenalex-snapshot
Enantioselective gold( i )-catalyzed cyclization/intermolecular nucleophilic additions of 1,5-enyne derivatives
inferred← citeshttps://doi.org/10.1039/d0qo00653jopenalex-snapshot
Nucleophile-assisted cyclization of β-propargylamino acrylic compounds catalyzed by gold( i ): a rapid construction of multisubstituted tetrahydropyridines and their fused derivatives
inferred← citeshttps://doi.org/10.1039/d1nj01821copenalex-snapshot
Sulfonyl radical-induced regioselective cyclization of 3-aza-1,5-enynes with sulfonyl chlorides to produce 1,2-dihydropyridines by copper catalysis
inferred← citeshttps://doi.org/10.1039/d1ra09298gopenalex-snapshot
Diastereoselective synthesis of new zwitterionic bicyclic lactams, scaffolds for construction of 2-substituted-4-hydroxy piperidine and its pipecolic acid derivatives
inferred← citeshttps://doi.org/10.1039/d2cs00101bopenalex-snapshot
Ketones as strategic building blocks for the synthesis of natural product-inspired compounds
inferred← citeshttps://doi.org/10.1039/d2dt03733eopenalex-snapshot
An MCM-41-immobilized dichloro(pyridine-2-carboxylato)gold( iii ) complex: an efficient and recyclable catalyst for the annulation of anthranils and ynamides
inferred← citeshttps://doi.org/10.1039/d2sc00989gopenalex-snapshot
Pyridine dicarbanion-bonded Ag 13 organometallic nanoclusters: synthesis and on-surface oxidative coupling reaction
inferred← citeshttps://doi.org/10.1039/d3md00411bopenalex-snapshot
Synthesis, biological activities, and future perspectives of steroidal monocyclic pyridines
inferred← citeshttps://doi.org/10.1039/d5cc02439kopenalex-snapshot
Wieland–Miescher ketone: a cornerstone in natural product synthesis
inferred← citeshttps://doi.org/10.1055/s-0036-1591965openalex-snapshot
Synthesis of C-Nor-D-homo-steroidal Alkaloids and Their Derivatives
inferred← citeshttps://doi.org/10.1055/sos-sd-115-00035openalex-snapshot
15.1.4 Pyridines (Update 2016)
inferred← citeshttps://doi.org/10.1070/rcr4815openalex-snapshot
Gold as a catalyst. Part II. Alkynes in the reactions of carbon – carbon bond formation
inferred← citeshttps://doi.org/10.1093/bulcsj/uoag054openalex-snapshot
Design and polymerization behavior of carbocyclic-fused (imino)pyridine-ligated late-transition-metal catalysts
inferred← citeshttps://doi.org/10.24959/ophcj.23.289263openalex-snapshot
The Synthesis of Diverse Annulated Pyridines with 6-Membered Functionalized Saturated Cycles for Medical Chemistry Research
inferred← citeshttps://doi.org/10.3389/fchem.2020.00772openalex-snapshot
Preliminary Study on Novel Expedient Synthesis of 5-Azaisocoumarins by Transition Metal-Catalyzed Cycloisomerization
inferred← citeshttps://doi.org/10.3390/m1712openalex-snapshot
Friedländer-Type Reaction of 4-Cholesten-3-one with 2′-Aminoacetophenone: Angular versus Linear Quinoline-Fused Steroids
inferred← citeshttps://doi.org/10.3390/molecules26113366openalex-snapshot
Synthesis of 4-Substituted-1,2-Dihydroquinolines by Means of Gold-Catalyzed Intramolecular Hydroarylation Reaction of N-Ethoxycarbonyl-N-Propargylanilines
inferred← citeshttps://doi.org/10.3390/molecules28124725openalex-snapshot
Synthesis of Nitrogen-Containing Heterocyclic Scaffolds through Sequential Reactions of Aminoalkynes with Carbonyls
inferred← citeshttps://doi.org/10.3762/bjoc.10.161openalex-snapshot
C–H-Functionalization logic guides the synthesis of a carbacyclopamine analog
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.72.246openalex-snapshot
Catalytic Consecutive Reactions of Alkynes for Syntheses of Heterocycles
inferred← citeshttps://doi.org/10.5772/intechopen.108127openalex-snapshot
The Chemistry of Benzo and Carbocyclic Derivatives of Pyridine
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