On the public citation graph

THE ACTION OF GRIGNARD REAGENTS ON OXIMES. I. THE ACTION OF PHENYLMAGNESIUM BROMIDE ON MIXED KETOXIMES

https://doi.org/10.1021/jo01214a012
0 signed · 27 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/9780470239704.ch2openalex-snapshot
Aziridines
inferred← citeshttps://doi.org/10.1002/9780470638859.conrr320openalex-snapshot
Hoch‐Campbell Reaction
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2516openalex-snapshot
Transition Metal Aziridination Catalysts
inferred← citeshttps://doi.org/10.1002/9783527625116.ch5openalex-snapshot
E
inferred← citeshttps://doi.org/10.1002/ajoc.201700056openalex-snapshot
Unprotected Aziridines: A Synthetic Overview
inferred← citeshttps://doi.org/10.1002/ardp.19743070412openalex-snapshot
C‐C‐Spaltung eines 1,2‐diarylsubstituierten Ketoxims bei der Umsetzung mit Äthylmagnesiumbromid
inferred← citeshttps://doi.org/10.1002/ejoc.200400613openalex-snapshot
Design and Evaluation of Inclusion Resolutions, Based on Readily Available Host Compounds
inferred← citeshttps://doi.org/10.1002/hlca.19760590542openalex-snapshot
20, 21‐Azirdin‐Steroide: Reaktion von Derivaten der Oxime von 5‐Pregnen‐20‐on,9β,10α‐5‐Pregnen‐20‐on und 9β,10α‐5,7‐Pregnadien‐20‐on mit Lithiumaluminiumhydrid und von 3β‐Hydroxy‐5‐pregnen‐20‐on‐oxim mit Grignard‐Verbindungen
inferred← citeshttps://doi.org/10.1007/bf00476529openalex-snapshot
Azirines in reactions involving the formation of a pyrrole ring (review)
inferred← citeshttps://doi.org/10.1007/bf00496592openalex-snapshot
Reaction of ketoximes with acetylene: A new general method for the synthesis of pyrroles (review)
inferred← citeshttps://doi.org/10.1016/b978-0-443-44508-8.00011-0openalex-snapshot
Synthesis of aziridines from different N-containing compounds
inferred← citeshttps://doi.org/10.1016/b978-012730945-3.50006-2openalex-snapshot
Addition of Organomagnesium Compounds to Carbon-Carbon Multiple Bonds
inferred← citeshttps://doi.org/10.1016/b978-012730945-3.50007-4openalex-snapshot
Addition of Organomagnesium Compounds to Carbon-Nitrogen Multiple Bonds
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/j.mencom.2014.11.020openalex-snapshot
2-(2-Ethynyl-1-aziranyl)-3,4-dihydro-2H-pyrrole: a one-pot assembly from isopropyl phenyl ketoxime and acetylene during the synthesis of 3H-pyrrole
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133488openalex-snapshot
An insight on iron mediated aziridination reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.085openalex-snapshot
One-pot assembly of 4-methylene-3-oxa-1-azabicyclo[3.1.0]hexanes from alkyl aryl(hetaryl) ketoximes, acetylene, and aliphatic ketones: a new three-component reaction
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)92311-7openalex-snapshot
Preparation of oxazine derivatives and 2,4-diarylpyrroles from methyl aryl ketoximes
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)84495-6openalex-snapshot
Obtention d'amines primaires par action d'organo-magnesiens sur l'acetoxime
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01042-0openalex-snapshot
Preparation of dihomoallylic secondary amines through samarium mediated allylation of oximes
inferred← citeshttps://doi.org/10.1016/s0065-2725(08)60003-3openalex-snapshot
Preparation of Pyrroles from Ketoximes and Acetylenes
inferred← citeshttps://doi.org/10.1016/s0065-3055(08)60068-4openalex-snapshot
Conjugate Addition of Grignard Reagents to Aromatic Systems
inferred← citeshttps://doi.org/10.1016/s0223-5234(00)00111-2openalex-snapshot
Synthesis, inhibitory activity towards human leukocyte elastase and molecular modelling studies of 1-carbamoyl-4-methyleneaminoxyazetidinones
inferred← citeshttps://doi.org/10.1021/ol2012204openalex-snapshot
Oxime Derivatives as α-Electrophiles. From α-Tetralone Oximes to Tetracyclic Frameworks
inferred← citeshttps://doi.org/10.1039/c5ob02425kopenalex-snapshot
Safe generation and use of bromine azide under continuous flow conditions – selective 1,2-bromoazidation of olefins
inferred← citeshttps://doi.org/10.1246/bcsj.36.1434openalex-snapshot
The Mechanism of Ethylenimine Formation by the Action of Grignard Reagents on Ketoximes
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.