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Copper-catalyzed Tandem Cyclization to Access 4-Aminoquinoline Derivatives

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What this work says

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

inferredcites →https://doi.org/10.1002/adsc.201100100openalex-snapshot
Copper‐Catalyzed Aerobic Oxidation of Amines to Imines under Neat Conditions with Low Catalyst Loading
inferredcites →https://doi.org/10.1002/adsc.201201107openalex-snapshot
Copper(I)‐Catalyzed Coupling Cyclization of Methyl Perfluoroalk‐2‐ynoates with 2‐Aminobenzonitriles: Synthesis of 2‐Perfluoroalkylated Quinolines
inferredcites →https://doi.org/10.1002/adsc.201800773openalex-snapshot
Copper‐Catalyzed Synthesis of 3‐NO2 Quinolines from o‐Azidobenzaldehyde and Nitro‐olefins and its Application in the Concise Synthesis of Quindolines
inferredcites →https://doi.org/10.1002/anie.201511385openalex-snapshot
Synthesis of Highly Functionalized 4‐Aminoquinolines
inferredcites →https://doi.org/10.1002/cber.188101402258openalex-snapshot
Ueber eine dem Chinolin homologe Base
inferredcites →https://doi.org/10.1002/cber.188201502219openalex-snapshot
Ueber o‐Amidobenzaldehyd
inferredcites →https://doi.org/10.1002/ejoc.201101786openalex-snapshot
Solvent‐Free Tandem Synthesis of 2‐Thiazolines and 2‐Oxazolines Catalyzed by a Copper Catalyst
inferredcites →https://doi.org/10.1002/ejoc.201200379openalex-snapshot
Base‐Promoted Heterocyclization of Fluorinated Alkynylphosphonates with Select ortho‐Aminobenzonitriles
inferredcites →https://doi.org/10.1002/ejoc.201403065openalex-snapshot
Heterocycle‐to‐Heterocycle Route to Quinoline‐4‐amines: Reductive Heterocyclization of 3‐(2‐Nitrophenyl)isoxazoles
inferredcites →https://doi.org/10.1002/ejoc.201601217openalex-snapshot
An Efficient One‐Pot Protocol for the Synthesis of Polysubstituted 4‐Amino‐iminocoumarins and 4‐Aminoquinolines by a Copper‐Catalyzed Three‐Component Reaction
inferredcites →https://doi.org/10.1007/s40261-018-0656-yopenalex-snapshot
Current and Future Use of Chloroquine and Hydroxychloroquine in Infectious, Immune, Neoplastic, and Neurological Diseases: A Mini-Review
inferredcites →https://doi.org/10.1016/j.apcata.2014.05.004openalex-snapshot
Bifunctional acid–base ionic liquid for the one-pot synthesis of fine chemicals: Thioethers, 2H-chromenes and 2H-quinoline derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2019.03.061openalex-snapshot
Synthesis and structure-activity relationships for new 6-fluoroquinoline derivatives with antiplasmodial activity
inferredcites →https://doi.org/10.1016/j.ejmech.2012.03.043openalex-snapshot
The synthesis of 2,5-bis(4-amidinophenyl)thiophene derivatives providing submicromolar-range inhibition of the botulinum neurotoxin serotype A metalloprotease
inferredcites →https://doi.org/10.1016/j.molcata.2007.11.013openalex-snapshot
Pd-catalyzed coupling of arylamines and 2-bromo-3,3,3-trifluoropropene
inferredcites →https://doi.org/10.1016/j.tet.2019.01.001openalex-snapshot
Metal-free synthesis of 2-difluoromethylated quinolines via DBU-promoted cascade michael addition / cyclization of methyl 4,4-difluorobut-2-ynoate with 2-aminobenzonitriles
inferredcites →https://doi.org/10.1016/j.tetlet.2007.02.031openalex-snapshot
An efficient, solvent-free approach to heteroarylcarbazoles: synthesis of 3-chromenylcarbazoles, 3,6-bis-(chromenyl)carbazoles and 3-quinolylcarbazoles
inferredcites →https://doi.org/10.1016/s0163-7258(97)00084-3openalex-snapshot
4-Aminoquinolines—Past, present, and future; A chemical perspective
inferredcites →https://doi.org/10.1021/acs.accounts.5b00060openalex-snapshot
Copper-Catalyzed Aerobic Oxidations of Organic Molecules: Pathways for Two-Electron Oxidation with a Four-Electron Oxidant and a One-Electron Redox-Active Catalyst
inferredcites →https://doi.org/10.1021/acs.accounts.7b00611openalex-snapshot
Copper-Catalyzed Oxidative Carbon–Carbon and/or Carbon–Heteroatom Bond Formation with O 2 or Internal Oxidants
inferredcites →https://doi.org/10.1021/acs.joc.7b02844openalex-snapshot
Modular Three-Component Synthesis of 4-Aminoquinolines via an Imidoylative Sonogashira/Cyclization Cascade
inferredcites →https://doi.org/10.1021/acs.orglett.7b01701openalex-snapshot
A Modular Synthesis of 4-Aminoquinolines and [1,3] N-to-C Rearrangement to Quinolin-4-ylmethanesulfonamides
inferredcites →https://doi.org/10.1021/acs.orglett.7b01798openalex-snapshot
Superacidic Cyclization of Activated Anthranilonitriles into 2-Unsubstituted-4-aminoquinolines
inferredcites →https://doi.org/10.1021/acs.orglett.8b03830openalex-snapshot
Gold-Catalyzed syn-1,2-Difunctionalization of Ynamides via Nitrile Activation
inferredcites →https://doi.org/10.1021/jm0002073openalex-snapshot
4-Aminoquinolines: Novel Nociceptin Antagonists with Analgesic Activity
inferredcites →https://doi.org/10.1021/jm00109a031openalex-snapshot
Synthesis and quantitative structure-activity relationship analysis of 2-(aryl or heteroaryl)quinolin-4-amines, a new class of anti-HIV-1 agents
inferredcites →https://doi.org/10.1021/jm900003copenalex-snapshot
Structure−Activity Relationships for a Series of Quinoline-Based Compounds Active against Replicating and NonreplicatingMycobacterium tuberculosis
inferredcites →https://doi.org/10.1021/jo030070zopenalex-snapshot
An Investigation of the Reaction of 2-Aminobenzaldehyde Derivatives with Conjugated Nitro-olefins: An Easy and Efficient Synthesis of 3-Nitro-1,2-dihydroquinolines and 3-Nitroquinolines
inferredcites →https://doi.org/10.1021/ma0100448openalex-snapshot
New Conjugated Polymers with Donor−Acceptor Architectures: Synthesis and Photophysics of Carbazole−Quinoline and Phenothiazine−Quinoline Copolymers and Oligomers Exhibiting Large Intramolecular Charge Transfer
inferredcites →https://doi.org/10.1021/np960250mopenalex-snapshot
HIV Inhibitory Natural Products. 26. Quinoline Alkaloids from Euodia roxburghiana
inferredcites →https://doi.org/10.1021/ol300896hopenalex-snapshot
Copper-Catalyzed Oxidative Cyclization of Enynes for the Synthesis of 4-Carbonyl-quinolines with O2
inferredcites →https://doi.org/10.1021/ol503156gopenalex-snapshot
Diverse Tandem Cyclization Reactions of o-Cyanoanilines and Diaryliodonium Salts with Copper Catalyst for the Construction of Quinazolinimine and Acridine Scaffolds
inferredcites →https://doi.org/10.1039/b509528jopenalex-snapshot
Quinoline, quinazoline and acridone alkaloids
inferredcites →https://doi.org/10.1039/b612168nopenalex-snapshot
Quinoline, quinazoline and acridonealkaloids
inferredcites →https://doi.org/10.1039/b613775jopenalex-snapshot
A highly effective one-pot synthesis of quinolines from o-nitroarylcarbaldehydes
inferredcites →https://doi.org/10.1039/c0gc00953aopenalex-snapshot
Sulfuric acid-modified PEG-6000 (PEG-OSO3H): an efficient, bio-degradable and reusable polymeric catalyst for the solvent-free synthesis of poly-substituted quinolines under microwave irradiation
inferredcites →https://doi.org/10.1039/c3ob41658eopenalex-snapshot
Cu-catalyzed tandem reactions of fluorinated alkynes with sulfonyl azides en route to 2-trifluoromethylquinolines
inferredcites →https://doi.org/10.1039/c4ra03666bopenalex-snapshot
Synthesis of 4-methyl-2,3-disubstituted quinoline scaffolds via environmentally benign Fe( iii ) catalysed sequential condensation, cyclization and aromatization of 1,3-diketone and 2-ethynylaniline
inferredcites →https://doi.org/10.1039/c9sc04305eopenalex-snapshot
Mechanistic insights into copper-catalyzed aerobic oxidative coupling of N–N bonds
inferredcites →https://doi.org/10.1039/jr9530003161openalex-snapshot
630. Some alkylquinoline-5: 8-quinones
inferredcites →https://doi.org/10.1055/s-2002-34412openalex-snapshot
Quinoline Alkaloids and Anti-Platelet Aggregation Constituents from the Leaves ofMelicope semecarpifolia
inferredcites →https://doi.org/10.1055/s-2006-942388openalex-snapshot
Interesting Results of Catalytic Hydrogenation of 3-(2-Nitrophenyl)isoxazoles and 3-(Nitrophenyl)-4,5-dihydroisoxazoles
inferredcites →https://doi.org/10.1056/nejm198611133152001openalex-snapshot
Oral Tetrahydroaminoacridine in Long-Term Treatment of Senile Dementia, Alzheimer Type
inferredcites →https://doi.org/10.1128/aac.00557-13openalex-snapshot
N -Cinnamoylated Aminoquinolines as Promising Antileishmanial Agents
inferredcites →https://doi.org/10.1177/106002809402800612openalex-snapshot
Tacrine: First Drug Approved for Alzheimer's Disease
inferredcites →https://doi.org/10.2174/138945006777709557openalex-snapshot
Quinoline Derivatives as Promising Inhibitors of Antibiotic Efflux Pump in Multidrug Resistant Enterobacter Aerogenes Isolates

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.4758293openalex-extracted
Dft Study of the Possible Mechanisms for the Synthesis of Α-Cyanophosphonates from Β-Nitrostyrenes
inferred← citeshttps://doi.org/10.1002/adts.202500379openalex-snapshot
DFT Study of the Possible Mechanisms for Synthesizing α‐Cyanophosphonates from β‐Nitrostyrenes
inferred← citeshttps://doi.org/10.1002/cjoc.70199openalex-snapshot
Switchable Annulation Pathways of Ynamides: Dual Catalytic Routes to 2H ‐1,6‐Benzoxazocines vs. TBSOTf ‐Catalyzed Selective 4‐Aminoquinoline Formation
inferred← citeshttps://doi.org/10.1002/jhet.4474openalex-snapshot
Tin ( IV ) chloride catalyzed one‐pot synthesis, characterization, and docking studies of 4‐aminoquinoline derivatives as Myt1 inhibitors
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02058openalex-snapshot
Photochemical Dearomative Vicinal Aminooximation of Heteroarenes with N -Nitrosamines
inferred← citeshttps://doi.org/10.1021/acsomega.6c01857openalex-snapshot
Gallium/Indium-Promoted [4 + 2] Annulation of 2-Aminobenzonitriles with Alkynes and Dimerization of 2-Aminobenzonitriles: One-Pot Access to 4-Aminoquinolines and 4-Amino-2-Arylquinazolines
inferred← citeshttps://doi.org/10.1039/d3qo00890hopenalex-snapshot
Metal-free [2 + 2] and [4 + 2] cycloadditions of N -aryl-substituted ynamides to construct functionalized aminocyclobutenes and 4-aminoquinolines
inferred← citeshttps://doi.org/10.1055/sos-sd-115-01218openalex-snapshot
15.4.5 Quinolinones and Related Systems (Update 2022)
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