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The Synthesis of Some 7-Chloro-4-(3-alkylaminopropylamino)-quinolines1
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4714055openalex-extracted
Sterically Hindered Amino Acid Ionic Liquids for Rapid and Efficient Capture of Co2
inferred← citeshttps://doi.org/10.1002/0471264180.or005.02openalex-snapshot
Cyanoethylation*Present address, Industrial Rayon Corporation, Cleveland, Ohio.
inferred← citeshttps://doi.org/10.1002/9780470125953.ch15openalex-snapshot
Preparation of Difunctional Compounds
inferred← citeshttps://doi.org/10.1002/9780470771082.ch2openalex-snapshot
The introduction of the amino group
inferred← citeshttps://doi.org/10.1002/cber.19650981039openalex-snapshot
Über die Cyanäthylierung N‐monosubstituierter Hydrazine
inferred← citeshttps://doi.org/10.1002/cber.19650981218openalex-snapshot
Umsetzungen mit cyanalkylierten Aminen
inferred← citeshttps://doi.org/10.1002/jhet.5570010512openalex-snapshot
Pyrimidines. XIV. Synthesis of 1‐substituted 5,6‐dihydrocytosines and an improved synthesis of 1‐substituted uracils
inferred← citeshttps://doi.org/10.1002/jhet.5570120220openalex-snapshot
Synthesis of 5,6,7,8‐tetrahydro‐5‐oxopyrido[2,3‐d]pyrimidine‐6‐carbonitriles and ‐6‐carboxylic acid esters
inferred← citeshttps://doi.org/10.1002/jps.2600631013openalex-snapshot
Excretion of Probenecid and its Metabolites in Bile and Urine of Rats
inferred← citeshttps://doi.org/10.1002/macp.1986.021870102openalex-snapshot
Polymers with tertiary amino groups obtained by the reaction between chloromethylated polystyrene and 3‐alkylaminopropionitrile
inferred← citeshttps://doi.org/10.1007/978-3-642-46057-9_2openalex-snapshot
Monomere Acryl- und Methacrylverbindungen
inferred← citeshttps://doi.org/10.1007/bf00473999openalex-snapshot
Synthesis of 1-substituted-3,3-dimethyl-3,4-dihydroisoquinolines
inferred← citeshttps://doi.org/10.1007/bf00506091openalex-snapshot
Synthesis and properties of 3-oxa-7,11-diazaspiro[5,6]dodecanes
inferred← citeshttps://doi.org/10.1007/bf00855366openalex-snapshot
Investigation of the kinetics of the reaction of cyanoethylated amines with phenylglycidyl ether
inferred← citeshttps://doi.org/10.1007/bf00963680openalex-snapshot
Principal directions of primary fragmentation of the cyanoethylated amines under electron impact
inferred← citeshttps://doi.org/10.1007/s11172-009-0296-8openalex-snapshot
Hydrazoic acid in the Mannich reaction
inferred← citeshttps://doi.org/10.1016/0006-2952(82)90273-8openalex-snapshot
Mode of action of 3-substituted propylamine cytotoxicity in culture cells
inferred← citeshttps://doi.org/10.1016/0040-4020(82)80213-5openalex-snapshot
13C-Nuclear Magnetic Resonance spectroscopy as a probe of enzyme environment—II
inferred← citeshttps://doi.org/10.1016/j.cej.2024.150771openalex-snapshot
Aqueous solutions of sterically hindered amino acid ionic liquids for rapid and efficient capture of CO2
inferred← citeshttps://doi.org/10.1016/j.tet.2008.10.071openalex-snapshot
Synthesis of novel deuterium labelled derivatives of N-alkylated polyamines
inferred← citeshttps://doi.org/10.1016/j.tet.2009.08.034openalex-snapshot
Synthesis of polyamino nitriles, en route to acylpolyamine neurotoxins, via the regioselective michael cyanoethylation of unprotected polyamines. Unusual behaviour of 1-(2-aminoethyl)piperazine
inferred← citeshttps://doi.org/10.1016/s0021-9673(01)80615-4openalex-snapshot
Gas chromatographic separation of aliphatic diamines
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)97009-1openalex-snapshot
Phosphoramides ω bromes synthese d'ethylene et propylene diamines
inferred← citeshttps://doi.org/10.1021/ac60034a018openalex-snapshot
Rapid Qualitative Method for Acrylonitrile
inferred← citeshttps://doi.org/10.1021/ac60034a019openalex-snapshot
Estimation of Acetic Acid as Impurity in Refined Formic Acid
inferred← citeshttps://doi.org/10.1021/jm100439popenalex-snapshot
Synthesis and Biological Characterization of Novel Charge-Deficient Spermine Analogues
inferred← citeshttps://doi.org/10.1021/jm701478aopenalex-snapshot
4-N-, 4-S-, and 4-O-Chloroquine Analogues: Influence of Side Chain Length and Quinolyl Nitrogen pKa on Activity vs Chloroquine Resistant Malaria
inferred← citeshttps://doi.org/10.1070/rc1961v030n11abeh003004openalex-snapshot
CYANOETHYLATION, DECYANOETHYLATION, AND TRANSCYANOETHYLATION
inferred← citeshttps://doi.org/10.1081/scc-120016308openalex-snapshot
Synthesis of Vinylogous β-Amino Esters fromN-(N,N-Dialkylaminoalkyl)benzotriazoles
inferred← citeshttps://doi.org/10.1111/j.1432-1033.1989.tb14515.xopenalex-snapshot
Inhibition of mammalian spermine synthase by N‐alkylated‐1,3‐diaminopropane derivatives in vitro and in cultured rat hepatoma cells
inferred← citeshttps://doi.org/10.1128/aac.00100-12openalex-snapshot
Sontochin as a Guide to the Development of Drugs against Chloroquine-Resistant Malaria
inferred← citeshttps://doi.org/10.1128/aac.40.8.1846openalex-snapshot
4-aminoquinoline analogs of chloroquine with shortened side chains retain activity against chloroquine-resistant Plasmodium falciparum
inferred← citeshttps://doi.org/10.1246/bcsj.43.3227openalex-snapshot
Intramolecular Hydrogen Bonds. XV. Intramolecular Interaction in N-Alkylaminoalkanonitriles
inferred← citeshttps://doi.org/10.15199/180.2020.1.1openalex-snapshot
Old drugs in new therapeutic indications - the case of chloroquine
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