On the public citation graph

Oxidation of Alcohols to Carbonyl Compounds with Diisopropyl Azodicarboxylate Catalyzed by Nitroxyl Radicals

0 signed · 113 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/3527603689openalex-snapshot

Modern Oxidation Methods

inferredcites →https://doi.org/10.1002/adsc.200404110openalex-snapshot

Organocatalytic Oxidations Mediated by Nitroxyl Radicals

inferredcites →https://doi.org/10.1002/adsc.200505102openalex-snapshot

An Efficient Catalytic Aerobic Oxidation of Alcohols in Water Using Hypervalent Iodine(V)

inferredcites →https://doi.org/10.1002/adsc.200800501openalex-snapshot

TEMPO‐tert‐Butyl Nitrite: An Efficient Catalytic System for Aerobic Oxidation of Alcohols

inferredcites →https://doi.org/10.1002/anie.200700604openalex-snapshot

Catalytic Oxidation of Organic Substrates by Molecular Oxygen and Hydrogen Peroxide by Multistep Electron Transfer—A Biomimetic Approach

inferredcites →https://doi.org/10.1002/chem.200701818openalex-snapshot

TEMPO/HCl/NaNO 2 Catalyst: A Transition‐Metal‐Free Approach to Efficient Aerobic Oxidation of Alcohols to Aldehydes and Ketones Under Mild Conditions

inferredcites →https://doi.org/10.1007/bf00853921openalex-snapshot

Reaction of iminoxyl radicals with some mineral acids

inferredcites →https://doi.org/10.1016/j.tet.2006.07.022openalex-snapshot

Mild and selective oxidation of alcohols to aldehydes and ketones using NaIO4/TEMPO/NaBr system under acidic conditions

inferredcites →https://doi.org/10.1016/j.tetlet.2009.01.080openalex-snapshot

DEAD-(cat)ZnBr2 an efficient system for the oxidation of alcohols to carbonyl compounds

inferredcites →https://doi.org/10.1016/s0040-4039(00)86993-2openalex-snapshot

Observations on the chemistry of the iodoxy group

inferredcites →https://doi.org/10.1021/cr800278zopenalex-snapshot

Mitsunobu and Related Reactions: Advances and Applications

inferredcites →https://doi.org/10.1021/ja00962a051openalex-snapshot

A New Hydrogen-Abstracting Reaction with Diethyl Azodicarboxylate

inferredcites →https://doi.org/10.1021/ja031765kopenalex-snapshot

Transition-Metal-Free: A Highly Efficient Catalytic Aerobic Alcohol Oxidation Process

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/jo00021a027openalex-snapshot

Organic oxoammonium salts. 3. A new convenient method for the oxidation of alcohols to aldehydes and ketones

inferredcites →https://doi.org/10.1021/jo00273a038openalex-snapshot

Oxidation of diols with alkali hypochlorites catalyzed by oxammonium salts under two-phase conditions

inferredcites →https://doi.org/10.1021/jo01278a049openalex-snapshot

A new hydrogen-abstracting reaction with diethyl azodicarboxylate

inferredcites →https://doi.org/10.1021/jo034276bopenalex-snapshot

Trichloroisocyanuric/TEMPO Oxidation of Alcohols under Mild Conditions: A Close Investigation

inferredcites →https://doi.org/10.1021/jo900486wopenalex-snapshot

An Expeditious Entry to 9-Azabicyclo[3.3.1]nonane N-Oxyl (ABNO): Another Highly Active Organocatalyst for Oxidation of Alcohols

inferredcites →https://doi.org/10.1021/jo9609790openalex-snapshot

Efficient and Highly Selective Oxidation of Primary Alcohols to Aldehydes by N-Chlorosuccinimide Mediated by Oxoammonium Salts

inferredcites →https://doi.org/10.1021/jo971046mopenalex-snapshot

A Versatile and Highly Selective Hypervalent Iodine (III)/2,2,6,6-Tetramethyl-1-piperidinyloxyl-Mediated Oxidation of Alcohols to Carbonyl Compounds

inferredcites →https://doi.org/10.1021/ol005792gopenalex-snapshot

Catalytic Synthesis of Aldehydes and Ketones under Mild Conditions Using TEMPO/Oxone

inferredcites →https://doi.org/10.1021/ol016501mopenalex-snapshot

A Very Mild and Chemoselective Oxidation of Alcohols to Carbonyl Compounds

inferredcites →https://doi.org/10.1021/ol0272444openalex-snapshot

Iodine as a Chemoselective Reoxidant of TEMPO: Application to the Oxidation of Alcohols to Aldehydes and Ketones

inferredcites →https://doi.org/10.1021/op900059xopenalex-snapshot

Industrial Oxidations with Organocatalyst TEMPO and Its Derivatives

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/10.1055/s-0029-1219202openalex-snapshot

In situ Formation of NOx and Br Anion for Aerobic Oxidation of Benzylic Alcohols without Transition Metal

inferredcites →https://doi.org/10.1246/bcsj.40.2380openalex-snapshot

Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium Salts

inferredcites →https://doi.org/10.1246/bcsj.40.935openalex-snapshot

Preparation of Esters of Phosphoric Acid by the Reaction of Trivalent Phosphorus Compounds with Diethyl Azodicarboxylate in the Presence of Alcohols

inferredcites →https://doi.org/10.1246/bcsj.50.2773openalex-snapshot

Efficient Methods for Oxidation of Alcohols

inferredcites →https://doi.org/10.1248/cpb.59.1570openalex-snapshot

9-Azanoradamantane N-Oxyl (Nor-AZADO): A Highly Active Organocatalyst for Alcohol Oxidation

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.4837417openalex-extracted

Synthesis and Characterization of a New Cage-Like Energetic Compound 9-Nitro-3,7-Dinitrato-9-Azanoradamantane

inferred← citeshttps://doi.org/10.1002/9780471264194.fos12196openalex-snapshot

2,2,6,6‐Tetramethylpiperidine 1‐oxyl, ( TEMPO )(2)

inferred← citeshttps://doi.org/10.1002/9780471264194.fos12196.pub2openalex-snapshot

2,2,6,6‐Tetramethylpiperidine 1‐oxyl, ( TEMPO )(2)

inferred← citeshttps://doi.org/10.1002/9781118662083.cot08-002openalex-snapshot

Formation of Aldehydes and Ketones by Oxidation

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz01362openalex-snapshot

AZADO, azado

inferred← citeshttps://doi.org/10.1002/adsc.201701351openalex-snapshot

Organocatalyzed Enantioselective Aldol and Henry Reactions Starting from Benzylic Alcohols

inferred← citeshttps://doi.org/10.1002/ajoc.201700138openalex-snapshot

Palladium(II) Bis(oxazoline) Complexes that Catalyze the Hydration of Alkynes

inferred← citeshttps://doi.org/10.1002/ange.201203799openalex-snapshot

Oxime Radical Promoted Dioxygenation, Oxyamination, and Diamination of Alkenes: Synthesis of Isoxazolines and Cyclic Nitrones

inferred← citeshttps://doi.org/10.1002/ange.201309634openalex-snapshot

Highly Chemoselective Aerobic Oxidation of Amino Alcohols into Amino Carbonyl Compounds

inferred← citeshttps://doi.org/10.1002/ange.201403110openalex-snapshot

Praktische aerobe Oxidationen von Alkoholen und Aminen mit dem homogenen Kupfer/TEMPO‐ und verwandten Katalysatorsystemen

inferred← citeshttps://doi.org/10.1002/anie.201203799openalex-snapshot

Oxime Radical Promoted Dioxygenation, Oxyamination, and Diamination of Alkenes: Synthesis of Isoxazolines and Cyclic Nitrones

inferred← citeshttps://doi.org/10.1002/anie.201309634openalex-snapshot

Highly Chemoselective Aerobic Oxidation of Amino Alcohols into Amino Carbonyl Compounds

inferred← citeshttps://doi.org/10.1002/anie.201403110openalex-snapshot

Practical Aerobic Oxidations of Alcohols and Amines with Homogeneous Copper/TEMPO and Related Catalyst Systems

inferred← citeshttps://doi.org/10.1002/asia.201403245openalex-snapshot

Highly Efficient Aerobic Oxidation of Alcohols by Using Less‐Hindered Nitroxyl‐Radical/Copper Catalysis: Optimum Catalyst Combinations and Their Substrate Scope

inferred← citeshttps://doi.org/10.1002/asia.202300814openalex-snapshot

A Metal‐Organic Complex Constructed from Co(II), Azo‐amide‐pyridyl and Benzenetricarboxylate Mixed Ligands: Efficient Catalysis for Selective Oxidation of Benzyl Alcohols to Benzyl Acids

inferred← citeshttps://doi.org/10.1002/chem.201203832openalex-snapshot

Radical‐Mediated Diamination of Alkenes with Phenylhydrazine and Azodicarboxylates: Highly Diastereoselective Synthesis of trans‐Diamines from Cycloalkenes

inferred← citeshttps://doi.org/10.1002/chem.201406256openalex-snapshot

NMO⋅TPB: A Selectivity Variation on the Ley–Griffith TPAP Oxidation

inferred← citeshttps://doi.org/10.1002/chin.201227032openalex-snapshot

ChemInform Abstract: Oxidation of Alcohols to Carbonyl Compounds with Diisopropyl Azodicarboxylate Catalyzed by Nitroxyl Radicals.

inferred← citeshttps://doi.org/10.1002/cjoc.201400141openalex-snapshot

4‐Benzamido‐TEMPO Catalyzed Oxidation of a Broad Range of Alcohols to the Carbonyl Compounds with NaBrO3 under Mild Conditions

inferred← citeshttps://doi.org/10.1002/cjoc.202200659openalex-snapshot

A New Polynitrogen‐Heterocyclic Scaffold 2,4,6, 8‐Tetraazanoradamantane Skeleton: Synthesis and Conversion of Its Functionalities

inferred← citeshttps://doi.org/10.1002/cssc.201402059openalex-snapshot

SBA‐15‐Functionalized 3‐Oxo‐ABNO as Recyclable Catalyst for Aerobic Oxidation of Alcohols under Metal‐Free Conditions

inferred← citeshttps://doi.org/10.1002/ejic.202000570openalex-snapshot

Reactions of Al‐N Based Active Lewis Pairs with Ketones and 1,2‐Diketones: Insertion into Al‐N Bonds, C‐C and C‐N Bond Formation and a Tricyclic Saturated Tetraaza Compound

inferred← citeshttps://doi.org/10.1002/ejoc.201301337openalex-snapshot

N‐Heterocyclic Carbene Catalysed Oxidative Coupling of Aldehydes with Alcohols/Thiols and One‐Pot Oxidation/Esterification of Allylic Alcohols

inferred← citeshttps://doi.org/10.1002/ejoc.201402991openalex-snapshot

Organocatalytic Oxidation of Secondary Alcohols Using 1,2‐Di(1‐naphthyl)‐1,2‐ethanediamine (NEDA)

inferred← citeshttps://doi.org/10.1002/ejoc.201701323openalex-snapshot

DEAD‐Promoted Oxidative Ugi‐Type Reaction Including an Unprecedented Ugi Amidation Assisted by Dicarboxylic Acids

inferred← citeshttps://doi.org/10.1002/ejoc.202000416openalex-snapshot

Ruthenium‐Catalyzed Dehydrogenation of Alcohols with Carbodiimide via a Hydrogen Transfer Mechanism

inferred← citeshttps://doi.org/10.1002/ejoc.202000785openalex-snapshot

Recent Developments in Transition Metal‐Free Cross‐Dehydrogenative Coupling Reactions for C–C Bond Formation

inferred← citeshttps://doi.org/10.1002/poc.3454openalex-snapshot

Redox-mediated oxidation of alcohols using Cl− /OCl− redox couple in biphasic media

inferred← citeshttps://doi.org/10.1002/slct.202200009openalex-snapshot

Heterogeneous Catalysis for Oxidation of Alcohol via 1‐Methyl‐2‐azaadamanane N ‐oxyl Immobilized on Magnetic Polystyrene Nanosphere

inferred← citeshttps://doi.org/10.1007/s11030-018-9868-6openalex-snapshot

Regioselective formation of 1,2,4-triazoles by the reaction of amidrazones in the presence of diethyl azodicarboxylate and catalyzed by triethylamine

inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00032-1openalex-snapshot

Aldehydes: α,β-Unsaturated Aldehydes

inferred← citeshttps://doi.org/10.1016/bs.adomc.2015.02.004openalex-snapshot

Catalytic Oxidation of Alcohols

inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.104280openalex-snapshot

Design, synthesis, crystal structures and biological evaluation of some 1,3-thiazolidin-4-ones as dual CDK2/EGFR potent inhibitors with potential apoptotic antiproliferative effects

inferred← citeshttps://doi.org/10.1016/j.enmf.2024.06.005openalex-snapshot

Synthesis and characterization of a new cage-like energetic compound 3,7-dinitrato-9-nitro-9-azanoradamantane

inferred← citeshttps://doi.org/10.1016/j.ica.2018.09.038openalex-snapshot

Metal-ligand cooperativity in a ruthenium(II) complex of bis-azoaromatic ligand for catalytic dehydrogenation of alcohols

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.10.001openalex-snapshot

Water soluble new bimetallic catalyst [CuZn(bz)3(bpy)2]PF6 in hydrogen peroxide mediated oxidation of alcohols to aldehydes/ketones and C-N functional groups

inferred← citeshttps://doi.org/10.1016/j.mtchem.2022.100872openalex-snapshot

Design and engineering of heterogeneous nitroxide-mediated catalytic systems for selective oxidation: Efficiency and sustainability

inferred← citeshttps://doi.org/10.1016/j.tet.2016.05.066openalex-snapshot

Biphasic copper-catalyzed C–H bond activation of arylalkanes to ketones with tert-butyl hydroperoxide in water at room temperature

inferred← citeshttps://doi.org/10.1016/j.tet.2019.07.021openalex-snapshot

Ambient-pressure hydrogenation of ketones and aldehydes by a metal-ligand bifunctional catalyst [Cp*Ir(2,2′-bpyO)(H2O)] without using base

inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.01.012openalex-snapshot

Aerobic oxidation of secondary alcohols in water with ABNO/tert-butyl nitrite/KPF6 catalytic system

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/10.1016/j.tetlet.2019.150994openalex-snapshot

3-BocNH-ABNO-catalyzed aerobic oxidation of alcohol at room temperature and atmospheric pressure

inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00212openalex-snapshot

Organic Synthesis Using Nitroxides

inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00763openalex-snapshot

Tetramethylpiperidine N -Oxyl (TEMPO), Phthalimide N -Oxyl (PINO), and Related N -Oxyl Species: Electrochemical Properties and Their Use in Electrocatalytic Reactions

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b00034openalex-snapshot

An Azoaromatic Ligand as Four Electron Four Proton Reservoir: Catalytic Dehydrogenation of Alcohols by Its Zinc(II) Complex

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01567openalex-snapshot

Diethyl Azodicarboxylate-Promoted Oxidative [3 + 2] Cycloaddition for the Synthesis of Pyrrolo[2,1-a]isoquinolines

inferred← citeshttps://doi.org/10.1021/acs.joc.3c01217openalex-snapshot

Oxidative Deprotection of Benzyl Protecting Groups for Alcohols by an Electronically Tuned Nitroxyl-Radical Catalyst

inferred← citeshttps://doi.org/10.1021/acs.joc.7b00643openalex-snapshot

One-Pot Cascade Synthesis of Quinazolin-4(3 H )-ones via Nickel-Catalyzed Dehydrogenative Coupling of o -Aminobenzamides with Alcohols

inferred← citeshttps://doi.org/10.1021/acs.joc.8b01868openalex-snapshot

Iminium Ion and N-Hydroxyimide as the Surrogate Components in DEAD-Promoted Oxidative Ugi Variant

inferred← citeshttps://doi.org/10.1021/acs.oprd.3c00020openalex-snapshot

Multigram, Chromatography-Free Synthesis of the Flavonol Morin

inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00456openalex-snapshot

Safe and Scalable Aerobic Oxidation by 2-Azaadamantan-2-ol (AZADOL)/NOx Catalysis: Large-Scale Preparation of Shi’s Catalyst

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01839openalex-snapshot

Chemoselective Oxidation ofp-Methoxybenzyl Ethers by an Electronically Tuned Nitroxyl Radical Catalyst

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01058openalex-snapshot

SBA-15 Supported 1-Methyl-2-azaadamanane N-Oxyl (1-Me-AZADO) as Recyclable Catalyst for Oxidation of Alcohol

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01087openalex-snapshot

Stereocontrolled Construction of ABCD Tetracyclic Ring System with Vicinal All-Carbon Quaternary Stereogenic Centers of Calyciphylline A Type Alkaloids

inferred← citeshttps://doi.org/10.1021/acscatal.3c01153openalex-snapshot

Diverse Site-Selective Transformation of Benzylic and Allylic Silyl Ethers via Organocatalytic Oxidation

inferred← citeshttps://doi.org/10.1021/cs400746mopenalex-snapshot

Efficient Aerobic Oxidation of Secondary Alcohols at Ambient Temperature with an ABNO/NO x Catalyst System

inferred← citeshttps://doi.org/10.1021/ja409241hopenalex-snapshot

Copper(I)/ABNO-Catalyzed Aerobic Alcohol Oxidation: Alleviating Steric and Electronic Constraints of Cu/TEMPO Catalyst Systems

inferred← citeshttps://doi.org/10.1021/jacs.4c11760openalex-snapshot

Oxoammonium-Catalyzed Ether Oxidation via Hydride Abstraction: Methodology Development and Mechanistic Investigation Using Paramagnetic Relaxation Enhancement NMR

inferred← citeshttps://doi.org/10.1021/jo400248yopenalex-snapshot

Allylic Substitution for Construction of a Chiral Quaternary Carbon Possessing an Aryl Group

inferred← citeshttps://doi.org/10.1021/jo4005684openalex-snapshot

Assisted Tandem Catalytic Cross Metathesis–Oxidation: In One Flask from Styrenes to 1,2-Diketones and Further to Quinoxalines

inferred← citeshttps://doi.org/10.1021/jo5008064openalex-snapshot

Selective Oxidation of Alcohols with Alkali Metal Bromides as Bromide Catalysts: Experimental Study of the Reaction Mechanism

inferred← citeshttps://doi.org/10.1021/jo5020917openalex-snapshot

Solar Photochemical Oxidation of Alcohols using Catalytic Hydroquinone and Copper Nanoparticles under Oxygen: Oxidative Cleavage of Lignin Models

inferred← citeshttps://doi.org/10.1021/ol3021435openalex-snapshot

Nitroxyl Radical/PhI(OAc)2: One-Pot Oxidative Cleavage of Vicinal Diols to (Di)Carboxylic Acids

inferred← citeshttps://doi.org/10.1021/ol403016popenalex-snapshot

Anaerobic Nitroxide-Catalyzed Oxidation of Alcohols Using the NO+/NO· Redox Pair

inferred← citeshttps://doi.org/10.1039/c2sc20699dopenalex-snapshot

Catalytic aerobic production of imines en route to mild, green, and concise derivatizations of amines

inferred← citeshttps://doi.org/10.1039/c3gc42124dopenalex-snapshot

A mild and highly efficient laccase-mediator system for aerobic oxidation of alcohols

inferred← citeshttps://doi.org/10.1039/c3oc90011hopenalex-snapshot

Synthetic methods: part (ii) oxidation and reduction methods

inferred← citeshttps://doi.org/10.1039/c4ra08133aopenalex-snapshot

NHC-catalyzed one-pot oxidation and oxidative esterification of allylic alcohols using TEMPO: the effect of alcohol additives

inferred← citeshttps://doi.org/10.1039/c5ob00270bopenalex-snapshot

Oxidative cleavage of allyl ethers by an oxoammonium salt

inferred← citeshttps://doi.org/10.1039/c5ra15286kopenalex-snapshot

Highly practical sodium( i )/azobenzene catalyst system for aerobic oxidation of benzylic alcohols

inferred← citeshttps://doi.org/10.1039/c6qo00249hopenalex-snapshot

Versatile and highly efficient oxidative C(sp 3 )–H bond functionalization of tetrahydroisoquinoline promoted by bifunctional diethyl azodicarboxylate (DEAD): scope and mechanistic insights

inferred← citeshttps://doi.org/10.1039/c6ra22108dopenalex-snapshot

Copper-catalyzed carbonylation of anilines by diisopropyl azodicarboxylate for the synthesis of carbamates

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/c9qo00017hopenalex-snapshot

Application of dialkyl azodicarboxylate frameworks featuring multi-functional properties

inferred← citeshttps://doi.org/10.1039/d5ob01174dopenalex-snapshot

Recent developments in nitroxide-mediated aerobic oxidations

inferred← citeshttps://doi.org/10.1055/a-1904-0249openalex-snapshot

Synthesis and Antiviral Evaluation of 2′,3′-β-C-Disubstituted Nucleoside Analogue ProTides to Test a Conformational Model of Potency Against Hepatitis C

inferred← citeshttps://doi.org/10.1055/s-0043-1773545openalex-snapshot

Accelerating Effect of the Addition of HFIP on the Oxidation of Alcohols Using TEMPO/PIDA

inferred← citeshttps://doi.org/10.1055/sos-sd-234-00022openalex-snapshot

1.2 Nitroxides in Organic Synthesis

inferred← citeshttps://doi.org/10.1063/5.0061891openalex-snapshot

Solvation of anthraquinone and TEMPO redox-active species in acetonitrile using a polarizable force field

inferred← citeshttps://doi.org/10.1070/rc2014v083n06abeh004419openalex-snapshot

Azodicarboxylates: synthesis and functionalization of organic compounds

inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.71.515openalex-snapshot

Development of Simple and Highly Efficient Aerobic Oxidation Method by Tuning Electrochemical and Steric Properties of Nitroxyl Radical Catalysts

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.