On the public citation graph

Synthesis of 1,3‐Cycloalkadienes from Cycloalkenes: Unprecedented Reactivity of Oxoammonium Salts

0 signed · 121 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/0470845813openalex-snapshot
The Diels–Alder Reaction
inferredcites →https://doi.org/10.1002/9783527609949openalex-snapshot
Terpenes
inferredcites →https://doi.org/10.1002/adsc.200600325openalex-snapshot
[2+2+2] Cycloaddition Reactions Catalyzed by Transition Metal Complexes
inferredcites →https://doi.org/10.1002/ange.200701631openalex-snapshot
Divergente Reaktionen an Racematen: katalytische, enantioselektive und regiodivergente Nitroso‐Diels‐Alder‐Reaktionen
inferredcites →https://doi.org/10.1002/ange.201412256openalex-snapshot
Access to Nitriles from Aldehydes Mediated by an Oxoammonium Salt
inferredcites →https://doi.org/10.1002/ange.201502505openalex-snapshot
Rhodium‐Catalyzed [3+2+2] and [2+2+2] Cycloadditions of Two Alkynes with Cyclopropylideneacetamides
inferredcites →https://doi.org/10.1002/anie.200701631openalex-snapshot
Divergent Reactions for Racemates: Catalytic, Enantioselective, and Regiodivergent Nitroso Diels–Alder Reactions
inferredcites →https://doi.org/10.1002/anie.201412256openalex-snapshot
Access to Nitriles from Aldehydes Mediated by an Oxoammonium Salt
inferredcites →https://doi.org/10.1002/anie.201502505openalex-snapshot
Rhodium‐Catalyzed [3+2+2] and [2+2+2] Cycloadditions of Two Alkynes with Cyclopropylideneacetamides
inferredcites →https://doi.org/10.1002/chem.200800903openalex-snapshot
Total Synthesis of (+)‐trans‐Dihydronarciclasine by a Catalytic Enantioselective Regiodivergent Nitroso Diels–Alder Reaction
inferredcites →https://doi.org/10.1002/chem.200901331openalex-snapshot
Enantioselective Nitroso‐Diels–Alder Reaction and Its Application for the Synthesis of (−)‐Peracetylated Conduramine A‐1
inferredcites →https://doi.org/10.1002/chem.201406067openalex-snapshot
Fullerene–Ionic‐Liquid Conjugates: A New Class of Hybrid Materials with Unprecedented Properties
inferredcites →https://doi.org/10.1002/ejoc.200600834openalex-snapshot
N‐Acetoxyammonium Ions – Reactive Intermediates in the Polonovski Reaction
inferredcites →https://doi.org/10.1002/ejoc.201200582openalex-snapshot
Synthesis of a New 2,3‐Diaminoconduritol with Conduritol F Structure
inferredcites →https://doi.org/10.1002/ejoc.201403012openalex-snapshot
Recent Advances in Stereoselective [2+2+2] Cycloadditions
inferredcites →https://doi.org/10.1002/ejoc.201500358openalex-snapshot
Niobium Complexes in Organic Transformations: From Stoichiometric Reactions to Catalytic [2+2+2] Cycloaddition Reactions
inferredcites →https://doi.org/10.1016/j.tet.2008.03.027openalex-snapshot
Selective tandem enyne metathesis for the synthesis of functionalized cycloheptadienes
inferredcites →https://doi.org/10.1016/j.tet.2013.05.075openalex-snapshot
A total synthesis of the epoxyquinone natural product cytosporin D
inferredcites →https://doi.org/10.1016/j.tet.2014.04.076openalex-snapshot
Highly functionalised cyclohexa-1,3-dienes by sulfonyl Nazarov reagents
inferredcites →https://doi.org/10.1016/j.tet.2015.05.016openalex-snapshot
Substituted 1,3-cyclohexadiene synthesis by NHC–Nickel(0) catalyzed [2+2+2] cycloaddition of 1,n-Enyne
inferredcites →https://doi.org/10.1016/j.tetlet.2010.06.121openalex-snapshot
Synthesis of lupinacidins A and B via sequential cycloaddition–double elimination
inferredcites →https://doi.org/10.1016/s0040-4039(00)76760-8openalex-snapshot
Erinacines A, B and C, strong stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum
inferredcites →https://doi.org/10.1016/s0040-4039(00)98312-6openalex-snapshot
Synthesis and diels-alder reactions of 5,5-dicyanocyclopentadiene: regioselective synthesis of 1,5-disubstituted-1,3-cyclohexadienes
inferredcites →https://doi.org/10.1016/s0040-4039(98)02700-2openalex-snapshot
Mycoepoxydiene represents a novel class of fungal metabolites
inferredcites →https://doi.org/10.1021/cr0203701openalex-snapshot
Synthesis and Conformational and Biological Aspects of Carbasugars
inferredcites →https://doi.org/10.1021/cr400686jopenalex-snapshot
Progress in the Synthesis and Transformations of Alkylidenecyclopropanes and Alkylidenecyclobutanes
inferredcites →https://doi.org/10.1021/ja00224a036openalex-snapshot
Through-bond interaction via cyclobutane relay orbitals as a means of extending conjugation. Synthesis of tricyclo[5.5.0.02,8]dodecatetraene, tricyclo[5.3.0.02,8]deca-3,5,9-triene, and 9,10-dimethylenetricyclo[5.3.0.02,8]deca-3,5-diene
inferredcites →https://doi.org/10.1021/ja01537a065openalex-snapshot
THE STRUCTURE OF GLIOTOXIN
inferredcites →https://doi.org/10.1021/ja0476922openalex-snapshot
Ring Synthesis by Stereoselective, Methylene-Free Enyne Cross Metathesis
inferredcites →https://doi.org/10.1021/ja0494306openalex-snapshot
Nickel-Catalyzed Intermolecular [3 + 2 + 2] Cocyclization of Ethyl Cyclopropylideneacetate and Alkynes
inferredcites →https://doi.org/10.1021/ja057306wopenalex-snapshot
A New Ru-Catalyzed Cascade Reaction Forming Polycyclic Cyclohexadienes from 1,6-Diynes and Alkenes
inferredcites →https://doi.org/10.1021/ja0620336openalex-snapshot
2-Azaadamantane N -Oxyl (AZADO) and 1-Me-AZADO: Highly Efficient Organocatalysts for Oxidation of Alcohols
inferredcites →https://doi.org/10.1021/ja110940copenalex-snapshot
Highly Efficient, Organocatalytic Aerobic Alcohol Oxidation
inferredcites →https://doi.org/10.1021/ja111067jopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed (4 + 2) Cycloaddition/Decarboxylation of Silyl Dienol Ethers with α,β-Unsaturated Acid Fluorides
inferredcites →https://doi.org/10.1021/ja2105043openalex-snapshot
Asymmetric Synthesis of Dihydroindanes by Convergent Alkoxide-Directed Metallacycle-Mediated Bond Formation
inferredcites →https://doi.org/10.1021/jo00041a003openalex-snapshot
An efficient synthesis of 1,3-cyclohexadienes from oxabicyclo[2.2.1]heptenes via tandem ring opening-Peterson elimination reactions
inferredcites →https://doi.org/10.1021/jo0100190openalex-snapshot
Diels−Alder Bioconjugation of Diene-Modified Oligonucleotides
inferredcites →https://doi.org/10.1021/jo01022a021openalex-snapshot
Synthesis of 1,3-Cyclohexadienes by the Reaction of Enamines with Methyl trans-2,4-Pentadienoate1
inferredcites →https://doi.org/10.1021/jo01255a056openalex-snapshot
Structure of (+)-occidentalol. Revision
inferredcites →https://doi.org/10.1021/jo048566jopenalex-snapshot
Asymmetric Total Syntheses of (+)-Mycoepoxydiene and Related Natural Product (−)-1893A: Application of One-Pot Ring-Opening/Cross/Ring-Closing Metathesis to Construct Their 9-Oxabicyclo[4.2.1]nona-2,4-diene Skeleton
inferredcites →https://doi.org/10.1021/jo060653jopenalex-snapshot
Sokodosides, Steroid Glycosides with an Isopropyl Side Chain, from the Marine Sponge Erylus placenta
inferredcites →https://doi.org/10.1021/jo2018872openalex-snapshot
Several Generations of Chemoenzymatic Synthesis of Oseltamivir (Tamiflu): Evolution of Strategy, Quest for a Process-Quality Synthesis, and Evaluation of Efficiency Metrics
inferredcites →https://doi.org/10.1021/jo300655popenalex-snapshot
Design, Synthesis, and Biological Activities of Some Branched Carbasugars: Construction of a Substituted 6-Oxabicyclo[3.2.1]nonane Skeleton
inferredcites →https://doi.org/10.1021/jo301258gopenalex-snapshot
An Approach to seco-Prezizaane Sesquiterpenoids: Enantioselective Total Synthesis of (+)-1S-Minwanenone
inferredcites →https://doi.org/10.1021/jo401889bopenalex-snapshot
Development of Enantioselective Synthetic Routes to the Hasubanan and Acutumine Alkaloids
inferredcites →https://doi.org/10.1021/jo402519mopenalex-snapshot
Oxoammonium Salt Oxidations of Alcohols in the Presence of Pyridine Bases
inferredcites →https://doi.org/10.1021/jo800735xopenalex-snapshot
Cobalt-Catalyzed Intermolecular [2 + 2 + 2] Cycloaddition for the Synthesis of 1,3-Cyclohexadienes
inferredcites →https://doi.org/10.1021/jo801344fopenalex-snapshot
Stereoselective Synthesis of Bishomo-inositols as Glycosidase Inhibitors
inferredcites →https://doi.org/10.1021/np2003066openalex-snapshot
Berkeleyones and Related Meroterpenes from a Deep Water Acid Mine Waste Fungus That Inhibit the Production of Interleukin 1-β from Induced Inflammasomes
inferredcites →https://doi.org/10.1021/np400174fopenalex-snapshot
C23 Steroids from the Venom of Bufo bufo gargarizans
inferredcites →https://doi.org/10.1021/ol061037copenalex-snapshot
Ga(III)-Catalyzed Cycloisomerization Strategy for the Synthesis of Icetexane Diterpenoids: Total Synthesis of (±)-Salviasperanol
inferredcites →https://doi.org/10.1021/ol062196zopenalex-snapshot
Ene-like Addition of an Oxoammonium Cation to Alkenes: Highly Selective Route to Allylic Alkoxyamines
inferredcites →https://doi.org/10.1021/ol201057ropenalex-snapshot
Total Synthesis of (+)-Grandifloracin by Iron Complexation of a Microbial Arene Oxidation Product
inferredcites →https://doi.org/10.1021/ol201273bopenalex-snapshot
Concise Entry to Both Enantiomers of 8-Oxabicyclo[3.2.1]oct-3-en-2-one Based on Novel Oxidative Etherification: Formal Synthesis of (+)-Sundiversifolide
inferredcites →https://doi.org/10.1021/ol2029417openalex-snapshot
Oxidative Conversion of Silyl Enol Ethers to α,β-Unsaturated Ketones Employing Oxoammonium Salts
inferredcites →https://doi.org/10.1021/ol902194qopenalex-snapshot
Synthesis and Antibacterial Properties of (−)-nor-Platencin
inferredcites →https://doi.org/10.1023/b:rujo.0000034978.81993.bdopenalex-snapshot
Synthesis of Substituted 1,3-Cyclohexadienes, Pyridine-2(1H)-thiones, and Thieno[2,3-d]pyrimidine- 4(3H)-thiones by the Michael Reaction
inferredcites →https://doi.org/10.1038/nprot.2013.028openalex-snapshot
Synthesis of 4-acetamido-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate and 4-acetamido-(2,2,6,6-tetramethyl-piperidin-1-yl)oxyl and their use in oxidative reactions
inferredcites →https://doi.org/10.1039/b807843bopenalex-snapshot
Oligonucleotide conjugation to a cell-penetrating (TAT) peptide by Diels–Alder cycloaddition
inferredcites →https://doi.org/10.1039/b822944aopenalex-snapshot
Oxoammonium salt/NaClO2: an expedient, catalytic system for one-pot oxidation of primary alcohols to carboxylic acids with broad substrate applicability
inferredcites →https://doi.org/10.1039/b900048hopenalex-snapshot
Asymmetric tandem Michael addition–ylide olefination reaction for the synthesis of optically active cyclohexa-1,3-diene derivatives
inferredcites →https://doi.org/10.1039/c1cs15029dopenalex-snapshot
Recent advances in [2+2+2] cycloaddition reactions
inferredcites →https://doi.org/10.1039/c4ob01922aopenalex-snapshot
Metal-catalyzed formation of 1,3-cyclohexadienes: a catalyst-dependent reaction
inferredcites →https://doi.org/10.1039/c5ob00270bopenalex-snapshot
Oxidative cleavage of allyl ethers by an oxoammonium salt
inferredcites →https://doi.org/10.1039/c5ob00729aopenalex-snapshot
A lactone-fused cyclohexadiene as a versatile platform for diversified synthesis of 5,6,5-tricyclic scaffolds
inferredcites →https://doi.org/10.1055/s-0030-1258027openalex-snapshot
Ph3P-Mediated Tandem Synthesis of Functionalized Cyclopentadienes from Primary Alkylamines and Acetylenic Esters
inferredcites →https://doi.org/10.1055/s-1993-25824openalex-snapshot
The Biosynthesis and Synthesis of Shikimic Acid, Chorismic Acid, and Related Compounds
inferredcites →https://doi.org/10.1111/jphp.12456openalex-snapshot
Saffron: a natural product with potential pharmaceutical applications
inferredcites →https://doi.org/10.1246/bcsj.67.1141openalex-snapshot
Enantioselective Preparation of 1,3-Cyclohexadiene and 1,4-Cycloheptadiene Derivatives: Synthesis of (+)-Dictyopterene C′
inferredcites →https://doi.org/10.1248/cpb.c13-00456openalex-snapshot
Discovery and Exploitation of AZADO: The Highly Active Catalyst for Alcohol Oxidation
inferredcites →https://doi.org/10.15227/orgsyn.047.0031openalex-snapshot
1,3-CYCLOHEXADIENE
inferredcites →https://doi.org/10.3987/com-08-s(n)60openalex-snapshot
Preparation of 1,3,3a,7a-Tetrahydroisothianaphthene and Its Application to Tetrahydrothiophene-Fused Porphyrin
inferredcites →https://doi.org/10.3998/ark.5550190.0013.326openalex-snapshot
Improved synthesis of the chrysomelid pheromone (6R,7S)-(+)-himachala-9,11-diene via spontaneous bromination and didehydrobromination of 2,6,6,9-tetramethyl-bicyclo[5.4.0]undec-8-ene

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.4520471openalex-extracted
inferred← citeshttps://doi.org/10.1002/9781118930786.ch3openalex-snapshot
Oxidation and Reduction
inferred← citeshttps://doi.org/10.1002/9781119288657.ch3openalex-snapshot
Oxidation and Reduction
inferred← citeshttps://doi.org/10.1002/9781119288657.ch9openalex-snapshot
Elimination Reactions
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz01362openalex-snapshot
AZADO, azado
inferred← citeshttps://doi.org/10.1002/9783527828166.ch4openalex-snapshot
Miscellaneous Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202100783openalex-snapshot
Oxoammonium Salt‐Mediated Vicinal Oxyazidation of Alkenes with NaN3: Access to β‐Aminooxy Azides
inferred← citeshttps://doi.org/10.1002/adsc.70696openalex-snapshot
Substrate‐Controlled Divergent Oxidative Transformations of Rigid Indene Scaffolds
inferred← citeshttps://doi.org/10.1002/ajoc.202300031openalex-snapshot
4‐Chloro‐2‐azaadamantane N‐Oxyl (4‐Cl‐AZADO): A Readily Preparable Organocatalyst for NOx Co‐catalyzed Aerobic Alcohol Oxidation
inferred← citeshttps://doi.org/10.1002/ange.201609686openalex-snapshot
Arenophile‐Mediated Dearomative Reduction
inferred← citeshttps://doi.org/10.1002/ange.201706963openalex-snapshot
Selective α‐Oxyamination and Hydroxylation of Aliphatic Amides
inferred← citeshttps://doi.org/10.1002/ange.202218961openalex-snapshot
Chemoselective 1,2‐Reduction and Regiodivergent Deuteration of Chromium‐Bound Arenes
inferred← citeshttps://doi.org/10.1002/ange.202500203openalex-snapshot
Flow Electroreductive Nickel‐Catalyzed Cyclopropanation of Alkenes Using gem ‐Dichloroalkanes
inferred← citeshttps://doi.org/10.1002/anie.201609686openalex-snapshot
Arenophile‐Mediated Dearomative Reduction
inferred← citeshttps://doi.org/10.1002/anie.201706963openalex-snapshot
Selective α‐Oxyamination and Hydroxylation of Aliphatic Amides
inferred← citeshttps://doi.org/10.1002/anie.202218961openalex-snapshot
Chemoselective 1,2‐Reduction and Regiodivergent Deuteration of Chromium‐Bound Arenes
inferred← citeshttps://doi.org/10.1002/anie.202500203openalex-snapshot
Flow Electroreductive Nickel‐Catalyzed Cyclopropanation of Alkenes Using gem ‐Dichloroalkanes
inferred← citeshttps://doi.org/10.1002/chem.201702512openalex-snapshot
Catalytic Oxygenative Allylic Transposition of Alkenes into Enones with an Azaadamantane‐Type Oxoammonium Salt Catalyst
inferred← citeshttps://doi.org/10.1002/ejoc.201701403openalex-snapshot
2,4,4,8,8‐Pentanitro‐2‐Azaadamantane: A High‐Density Energetic Compound
inferred← citeshttps://doi.org/10.1002/pola.28939openalex-snapshot
Ring opening metathesis polymerization (ROMP) and thio‐bromo “click” chemistry approach toward the preparation of flame‐retardant polymers
inferred← citeshttps://doi.org/10.1002/slct.202103240openalex-snapshot
Synthesis of Novel 1,3‐Cyclohexadiene Derivatives Bearing 2‐Oxo‐Quinoline Moiety via a 4‐CR Strategy**
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00013-5openalex-snapshot
1,2-Oxazines and Their Benzo Derivatives
inferred← citeshttps://doi.org/10.1016/j.rechem.2021.100214openalex-snapshot
Reinvestigation of 2,2,6,6-tetramethylpiperidine-1-oxoammonium mono- and tribromide: From old compounds to new findings
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133226openalex-snapshot
Chemoselective oxidation of alcohols in the presence of amines using an oxoammonium salt
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133739openalex-snapshot
Iron-Catalyzed Oxidation of Phthalimide-Derived Hydroxylactams and Isoindolinones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.11.002openalex-snapshot
Oxoammonium salt-mediated oxidative nitriles synthesis from aldehydes with ammonium acetate
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00212openalex-snapshot
Organic Synthesis Using Nitroxides
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00613openalex-snapshot
Stereoselective Synthesis of cis-2-Ene-1,4-diones via Aerobic Oxidation of Substituted Furans Catalyzed by ABNO/HNO3
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01302openalex-snapshot
TEMPO as a Hydrogen Atom Transfer Catalyst for Aerobic Dehydrogenation of Activated Alkanes to Alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02414openalex-snapshot
Convergent and Scalable Synthesis of the ABCDE-Ring Fragment of Caribbean Ciguatoxin C-CTX-1
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02558openalex-snapshot
Dehydrogenative Aza-[4 + 2] Cycloaddition of Amines with 1,3-Dienes via Dual Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03253openalex-snapshot
Oxoammonium Salt-Promoted Multifunctionalization of Saturated Cyclic Amines Based On β-Oxo Cyclic Iminium Ion Intermediates
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04851openalex-snapshot
Total Synthesis of Melonine
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01402openalex-snapshot
K 2 S 2 O 8 /TEMPO-Induced Cascade Oxidative Cyclization/1,2-Migration of Electron-Deficient Groups: Strategy for the Construction of 1 H -Pyrrol-2(3 H )-ones
inferred← citeshttps://doi.org/10.1021/acscatal.9b00832openalex-snapshot
4-HO-TEMPO-Catalyzed Redox Annulation of Cyclopropanols with Oxime Acetates toward Pyridine Derivatives
inferred← citeshttps://doi.org/10.1021/acsomega.3c06902openalex-snapshot
Comprehensive Structural and Electronic Properties of 2-Azaadamantane N-Oxyl Derivatives Correlated with Their Catalytic Ability
inferred← citeshttps://doi.org/10.1021/jacs.3c13864openalex-snapshot
Asymmetric Synthesis of Nidulalin A and Nidulaxanthone A: Selective Carbonyl Desaturation Using an Oxoammonium Salt
inferred← citeshttps://doi.org/10.1021/jacs.5c15942openalex-snapshot
Temporary Molybdenum η 6 -Coordination Enables Selective and General Dearomative 1,2-Hydrofunctionalization of Benzenes
inferred← citeshttps://doi.org/10.1039/c7cc08957kopenalex-snapshot
IBX as a catalyst for dehydration of hydroperoxides: green entry to α,β-unsaturated ketones via oxygenative allylic transposition
inferred← citeshttps://doi.org/10.1039/c8sc01410hopenalex-snapshot
CuCl/TMEDA/nor-AZADO-catalyzed aerobic oxidative acylation of amides with alcohols to produce imides
inferred← citeshttps://doi.org/10.1039/d1ob00965fopenalex-snapshot
Tandem elimination-oxidation of tertiary benzylic alcohols with an oxoammonium salt
inferred← citeshttps://doi.org/10.1039/d2cc06301hopenalex-snapshot
Sequential click modification of a lithium-ion endohedral fullerene connecting small molecules through a dieneazide linker
inferred← citeshttps://doi.org/10.1039/d3dt01471aopenalex-snapshot
Reactivity regulation for olefin metathesis-catalyzing ruthenium complexes with sulfur atoms at the terminal of 2-alkoxybenzylidene ligands
inferred← citeshttps://doi.org/10.1039/d4ob00696hopenalex-snapshot
Access to cyclohexadiene and benzofuran derivatives via catalytic arene cyclopropanation of α-cyanodiazocarbonyl compounds
inferred← citeshttps://doi.org/10.1039/d5gc00115copenalex-snapshot
Synthesis of catechols from cyclohexanones via acid-regulated dual oxidative transformations with TEMPO
inferred← citeshttps://doi.org/10.1055/s-0040-1719856openalex-snapshot
Hydrohalogenation of Unactivated Alkenes Using a Methanesulfonic Acid/Halide Salt Combination
inferred← citeshttps://doi.org/10.1126/science.adq8029openalex-snapshot
A chiral hydrogen atom abstraction catalyst for the enantioselective epimerization of meso -diols
inferred← citeshttps://doi.org/10.3987/rev-21-sr(r)2openalex-snapshot
The Utility of Oxoammonium Species in Organic Synthesis: Beyond Alcohol Oxidation
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.