On the public citation graph

AMINO ALCOHOLS. VII. PHENOLIC ARYLPROPANOLAMINES

https://doi.org/10.1021/ja01362a033
0 signed · 39 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

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.4675520openalex-extracted
inferred← citeshttps://doi.org/10.1002/0471264180.or007.06openalex-snapshot
The Nitrosation of Aliphatic Carbon Atoms
inferred← citeshttps://doi.org/10.1002/0471264180.os013.25openalex-snapshot
o‐Propiophenol andp‐Propiophenol
inferred← citeshttps://doi.org/10.1002/0471701343.sdp01235openalex-snapshot
α‐(1‐Aminoethyl)‐2,4‐Dimethoxybenzyl Alcohol Hydrochloride 63991‐14‐0
inferred← citeshttps://doi.org/10.1002/0471701343.sdp01251openalex-snapshot
α‐(1‐Aminoethyl)‐4‐Methoxybenzyl Alcohol Hydrochloride 63991‐23‐1
inferred← citeshttps://doi.org/10.1002/0471701343.sdp01515openalex-snapshot
Aminopropanol Pyrocatecholhydrochloride 138‐61‐4
inferred← citeshttps://doi.org/10.1002/0471701343.sdp17177openalex-snapshot
p ‐Methyl‐ m ‐Hydroxy‐Phenyl‐Propanol‐Amine Hydrochloride 63991‐31‐1
inferred← citeshttps://doi.org/10.1002/bscb.19520611102openalex-snapshot
Synthèses au moyen de dérivés organocadmiques Préparation de quelques méta‐hydroxyacylophénones ALK‐CO‐C6H4‐OH (m)
inferred← citeshttps://doi.org/10.1002/cber.19430760505openalex-snapshot
Über eine neue Synthese des α‐[3.4 ‐ Dioxy ‐ phenyl] ‐ β‐amino‐propanols
inferred← citeshttps://doi.org/10.1002/cber.19430761211openalex-snapshot
Synthetische Norephedrin‐ und Isochinolin‐Abkömmlinge
inferred← citeshttps://doi.org/10.1002/hlca.19660490123openalex-snapshot
Fluoreszenzmethoden zur histochemischen Sichtbarmachung von Monoaminen. 6. Identifizierung der fluoreszierenden Produkte aus m‐Hydroxyphenyläthylaminen und Formaldehyd
inferred← citeshttps://doi.org/10.1002/jlac.19586130111openalex-snapshot
Zur Reduktion Von Derivaten Des β‐ Und p‐dl‐Hydroxy‐α‐Amino‐Propiophenons. Partielle asymmetrische Synthesen von Ephedrinkörpern unter dem Einfluß von Seitenketten‐ und Kernsubstituenten V
inferred← citeshttps://doi.org/10.1002/jlcr.2590040111openalex-snapshot
Synthesis of tritium labelled metaraminol, α‐ methylnoradrenaline and their corresponding β‐ desoxyderivatives
inferred← citeshttps://doi.org/10.1002/jps.3030370513openalex-snapshot
A contribution to the pharmacodynamics and chemistry of glycinanilide
inferred← citeshttps://doi.org/10.1002/jps.3080210507openalex-snapshot
Alkaloidal reagents. III. Propadrin, its homologs and derivatiives
inferred← citeshttps://doi.org/10.1002/jps.3080220903openalex-snapshot
The Pharmacological Action of ten Amines Related to Ephedrine and Tryptamine**From the Lilly Research Laboratories, Eli Lilly and Company, Indianapolis
inferred← citeshttps://doi.org/10.1002/recl.19490680811openalex-snapshot
La p‐Hydroxypropiophénone, Ses Analogues et Leurs Dérivés
inferred← citeshttps://doi.org/10.1002/recl.19590780103openalex-snapshot
Synthesis of β‐phenylethylamine derivatives VI Stereoisomers of 1‐(4′‐hydroxyphenyl)‐2‐(1″‐methyl‐2″‐phenoxyethylamino) propanol‐1
inferred← citeshttps://doi.org/10.1007/978-1-4020-9787-4_23openalex-snapshot
Aromatic Ketones Containing One Propionyl Group
inferred← citeshttps://doi.org/10.1007/978-1-4757-2085-3_1openalex-snapshot
A
inferred← citeshttps://doi.org/10.1007/978-3-642-57995-0_3openalex-snapshot
C
inferred← citeshttps://doi.org/10.1007/978-3-662-36309-6_8openalex-snapshot
Oxyoxoverbindungen
inferred← citeshttps://doi.org/10.1007/978-3-7091-3245-6_8openalex-snapshot
Oxyoxoverbindungen
inferred← citeshttps://doi.org/10.1007/bf00474323openalex-snapshot
Epimination of olefins by means of 3,3-pentamethyleneoxaziridine ? A one-step synthesis of aziridines
inferred← citeshttps://doi.org/10.1016/0030-4220(53)90168-6openalex-snapshot
The trend to more potent local anesthetic solutions in dentistry
inferred← citeshttps://doi.org/10.1016/0091-3057(84)90121-7openalex-snapshot
Discriminative stimulus properties of S(−)- and R(+)-cathinone, (+)-cathine and several structural modifications
inferred← citeshttps://doi.org/10.1016/b978-0-12-395532-6.50012-xopenalex-snapshot
Oximes
inferred← citeshttps://doi.org/10.1016/b978-0-12-605355-5.50012-4openalex-snapshot
Hydrogenation of Oximes
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.05.033openalex-snapshot
MAO inhibition by arylisopropylamines: the effect of oxygen substituents at the β-position
inferred← citeshttps://doi.org/10.1016/j.forc.2024.100558openalex-snapshot
Forensic implications of novel synthesis of cathinone derivatives by Neber and modified Neber rearrangements
inferred← citeshttps://doi.org/10.1016/s0021-9673(00)85511-9openalex-snapshot
Analysis of perfluoroacyl derivatives of ephedrine, pseudoephedrine and analogues by gas chromatography and mass spectrometry
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)91103-2openalex-snapshot
δ Lactones from δ-ketoesters-II
inferred← citeshttps://doi.org/10.1016/s0379-0738(97)02133-6openalex-snapshot
The characterization of some 3,4-methylenedioxycathinone (MDCATH) homologs
inferred← citeshttps://doi.org/10.1039/p19940000903openalex-snapshot
Ozone-mediated nitration of aromatic ketones and related compounds with nitrogen dioxide
inferred← citeshttps://doi.org/10.1080/00304949209356226openalex-snapshot
USES OF THE FRIES REARRANGEMENT FOR THE PREPARATION OF HYDROXYARYLKETONES. A REVIEW
inferred← citeshttps://doi.org/10.1080/00397918808081315openalex-snapshot
Oxidation of Active Methylene Compounds by Pyridinium Chlorochromate
inferred← citeshttps://doi.org/10.1124/jpet.121.000978openalex-snapshot
Attenuation of Response to Repeated Drug Administration: A Proposal for Differentiating Tachyphylaxis and Tolerance
inferred← citeshttps://doi.org/10.1246/bcsj.47.2255openalex-snapshot
Photochemical Reactions of Some 1-Aryl-1,2-propanediones
inferred← citeshttps://doi.org/10.3109/00498257909038744openalex-snapshot
Interindividual and interspecies variation in the metabolism of the hallucinogen 4-methoxyamphetamine
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.