On the public citation graph

Synthesis of Aristolactam Derivatives via Benzannulation of 2-Bromobenzaldehydes and Indolin-1-ones

0 signed · 28 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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 this work says

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

inferredcites →https://doi.org/10.1002/ejoc.201001746openalex-snapshot
Neighbouring Formyl Group Assisted Oxidation of o‐Alkynylarenecarbaldehydes by an Iodine/Water System
inferredcites →https://doi.org/10.1007/bf02975156openalex-snapshot
Cytotoxic alkaloids fromHouttuynia cordate
inferredcites →https://doi.org/10.1016/0031-9422(88)80226-7openalex-snapshot
Aristolactams and 4,5-dioxoaporphines from Piper longum
inferredcites →https://doi.org/10.1016/j.bmc.2006.10.034openalex-snapshot
Discovery and synthesis of new immunosuppressive alkaloids from the stem of Fissistigma oldhamii (Hemsl.) Merr.
inferredcites →https://doi.org/10.1016/j.bmcl.2009.04.020openalex-snapshot
Synthesis of aristolactam analogues and evaluation of their antitumor activity
inferredcites →https://doi.org/10.1016/j.bse.2016.02.028openalex-snapshot
Aristolactam-type alkaloids and aristolochic acids from Aristolochia moupinensis and Aristolochia cathcartii
inferredcites →https://doi.org/10.1016/j.fitote.2015.04.005openalex-snapshot
A 2H-tetrahydropyran derivative and bioactive constituents from the bark of Goniothalamus elegants Ast
inferredcites →https://doi.org/10.1016/j.indcrop.2018.05.052openalex-snapshot
Chemical composition, antimicrobial and antimycobacterial activities of Aristolochia triangularis Cham. from Brazil
inferredcites →https://doi.org/10.1016/j.phytochem.2012.09.019openalex-snapshot
Pyridocoumarin, aristolactam and aporphine alkaloids from the Australian rainforest plant Goniothalamus australis
inferredcites →https://doi.org/10.1016/j.phytochem.2018.06.017openalex-snapshot
Aporphine Alkaloids from Illigera aromatica from Guangxi Province, China
inferredcites →https://doi.org/10.1016/j.phytol.2018.01.009openalex-snapshot
Cytotoxic lactam and naphthoquinone alkaloids from roots of Goniothalamus lanceolatus Miq.
inferredcites →https://doi.org/10.1021/acs.joc.9b00452openalex-snapshot
Phosphazene Superbase-Mediated Regio- and Stereoselective Iodoaminocyclization of 2-(1-Alkynyl)benzamides for the Synthesis of Isoindolin-1-ones
inferredcites →https://doi.org/10.1021/acs.orglett.8b03409openalex-snapshot
Pd(II)/Cu(II)-Catalyzed Regio- and Stereoselective Synthesis of (E)-3-Arylmethyleneisoindolin-1-ones Using Air as the Terminal Oxidant
inferredcites →https://doi.org/10.1021/jo00009a010openalex-snapshot
Intermolecular benzyne cycloaddition (IBC) approach to aporphinoids. Total syntheses of norcepharadione B, cepharadione B, dehydroanonaine, duguenaine, dehydronornuciferine, pontevedrine, O-methylatheroline, lysicamine, and alkaloid PO-3
inferredcites →https://doi.org/10.1021/ol801291kopenalex-snapshot
Total Synthesis of Aristolactams via a One-Pot Suzuki−Miyaura Coupling/Aldol Condensation Cascade Reaction
inferredcites →https://doi.org/10.1039/a708927iopenalex-snapshot
β-Phenylethylamines and the isoquinoline alkaloids
inferredcites →https://doi.org/10.1039/b303648kopenalex-snapshot
Naturally occurring aristolactams, aristolochic acids and dioxoaporphines and their biological activities
inferredcites →https://doi.org/10.1039/c3np70114jopenalex-snapshot
Naturally occurring aristolochic acid analogues and their toxicities
inferredcites →https://doi.org/10.1039/c7sc00161dopenalex-snapshot
Total synthesis of aristolactam alkaloids via synergistic C–H bond activation and dehydro-Diels–Alder reactions
inferredcites →https://doi.org/10.1039/d3nj02565aopenalex-snapshot
The isolation-biological activities (2014–2022), bio, semi, total synthesis (1978–2022) and SAR studies of a potential naturally engineered scaffold aristolactam
inferredcites →https://doi.org/10.1039/d3ob01603jopenalex-snapshot
A deconstruction–reconstruction strategy to access 1-naphthol derivatives: application to the synthesis of aristolactam scaffolds
inferredcites →https://doi.org/10.1039/d4ob01024hopenalex-snapshot
Transition metal-catalyzed transformations of 2-formylarylboronic acids
inferredcites →https://doi.org/10.1055/s-2004-818964openalex-snapshot
Aristolactam BII ofSaururus chinensisAttenuates Glutamate-Induced Neurotoxicity in Rat Cortical Cultures Probably by Inhibiting Nitric Oxide Production
inferredcites →https://doi.org/10.1055/s-2005-864155openalex-snapshot
New Cytotoxic Cyclobutanoid Amides, a New Furanoid Lignan and Anti-Platelet Aggregation Constituents fromPiper arborescens
inferredcites →https://doi.org/10.1080/10286020.2016.1268129openalex-snapshot
Four new compounds from the rhizome of Aristolochia championii
inferredcites →https://doi.org/10.1080/14786419.2017.1396588openalex-snapshot
Marcanine G, a new cytotoxic 1-azaanthraquinone from the stem bark of Goniothalamus marcanii Craib
inferredcites →https://doi.org/10.1080/14786419.2017.1423301openalex-snapshot
Aristololactam derivatives from the fruits of Aristolochia contorta Bunge
inferredcites →https://doi.org/10.1093/carcin/bgw045openalex-snapshot
Sulfotransferase-1A1-dependent bioactivation of aristolochic acid I andN-hydroxyaristolactam I in human cells
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.