On the public citation graph

l -Proline: An Efficient Catalyst for Transamidation of Carboxamides with Amines

0 signed · 226 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/352760068xopenalex-snapshot

Peptides: Chemistry and Biology

inferredcites →https://doi.org/10.1002/9781118662083openalex-snapshot

Comprehensive Organic Transformations

inferredcites →https://doi.org/10.1002/adsc.201100100openalex-snapshot

Copper‐Catalyzed Aerobic Oxidation of Amines to Imines under Neat Conditions with Low Catalyst Loading

inferredcites →https://doi.org/10.1002/anie.200353461openalex-snapshot

Efficient Hydration of Nitriles to Amides in Water, Catalyzed by Ruthenium Hydroxide Supported on Alumina

inferredcites →https://doi.org/10.1002/anie.200400650openalex-snapshot

In the Golden Age of Organocatalysis

inferredcites →https://doi.org/10.1002/anie.200453716openalex-snapshot

Enantioselective Organocatalytic Direct Aldol Reactions of α‐Oxyaldehydes: Step One in a Two‐Step Synthesis of Carbohydrates

inferredcites →https://doi.org/10.1002/anie.200705643openalex-snapshot

Asymmetric Direct Amide Synthesis by Kinetic Amine Resolution: A Chiral Bifunctional Aminoboronic Acid Catalyzed Reaction between a Racemic Amine and an Achiral Carboxylic Acid

inferredcites →https://doi.org/10.1002/anie.200800366openalex-snapshot

Rh I ‐Catalyzed Hydration of Organonitriles under Ambient Conditions

inferredcites →https://doi.org/10.1002/anie.200804757openalex-snapshot

Catalyzed Dehydrogenative Coupling of Primary Alcohols with Water, Methanol, or Amines

inferredcites →https://doi.org/10.1002/anie.201005874openalex-snapshot

One‐Pot Formation of CC and CN Bonds through Palladium‐Catalyzed Dual CH Activation: Synthesis of Phenanthridinones

inferredcites →https://doi.org/10.1002/anie.201107110openalex-snapshot

Heterogeneously Catalyzed Synthesis of Primary Amides Directly from Primary Alcohols and Aqueous Ammonia

inferredcites →https://doi.org/10.1002/anie.201107348openalex-snapshot

Transamidation of Primary Amides with Amines Using Hydroxylamine Hydrochloride as an Inorganic Catalyst

inferredcites →https://doi.org/10.1002/anie.201108599openalex-snapshot

Efficient Copper(II)‐Catalyzed Transamidation of Non‐Activated Primary Carboxamides and Ureas with Amines

inferredcites →https://doi.org/10.1002/chem.200901231openalex-snapshot

Gold Activation of Nitriles: Catalytic Hydration to Amides

inferredcites →https://doi.org/10.1007/s00726-011-0899-xopenalex-snapshot

TG2 transamidating activity acts as a reostat controlling the interplay between apoptosis and autophagy

inferredcites →https://doi.org/10.1016/0092-8674(93)90718-6openalex-snapshot

Human genetic diseases due to codon reiteration: Relationship to an evolutionary mechanism

inferredcites →https://doi.org/10.1016/j.jorganchem.2010.09.059openalex-snapshot

Efficient synthesis of di- and trisubstituted 2-aryloxazoles via ytterbium(III) triflate catalyzed cyclization of tertiary propargylic alcohols with aryl amides

inferredcites →https://doi.org/10.1016/j.tet.2011.06.045openalex-snapshot

Practical synthesis of amides from alkynyl bromides, amines, and water

inferredcites →https://doi.org/10.1016/s0006-291x(02)00582-xopenalex-snapshot

GTP is required to stabilize and display transamidation activity of transglutaminase 2

inferredcites →https://doi.org/10.1021/cr950005sopenalex-snapshot

Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides

inferredcites →https://doi.org/10.1021/ja0174231openalex-snapshot

The Proline-Catalyzed Direct Asymmetric Three-Component Mannich Reaction: Scope, Optimization, and Application to the Highly Enantioselective Synthesis of 1,2-Amino Alcohols

inferredcites →https://doi.org/10.1021/ja028242hopenalex-snapshot

Catalytic Transamidation under Moderate Conditions

inferredcites →https://doi.org/10.1021/ja056399eopenalex-snapshot

Copper-Catalyzed Hydrative Amide Synthesis with Terminal Alkyne, Sulfonyl Azide, and Water

inferredcites →https://doi.org/10.1021/ja060331xopenalex-snapshot

Mechanism of Al III -Catalyzed Transamidation of Unactivated Secondary Carboxamides

inferredcites →https://doi.org/10.1021/ja064315bopenalex-snapshot

Highly Efficient Oxidative Amidation of Aldehydes with Amine Hydrochloride Salts

inferredcites →https://doi.org/10.1021/ja0650293openalex-snapshot

TiIV-Mediated Reactions between Primary Amines and Secondary Carboxamides: Amidine Formation Versus Transamidation

inferredcites →https://doi.org/10.1021/ja066728iopenalex-snapshot

Efficient Transamidation of Primary Carboxamides by in Situ Activation with N,N-Dialkylformamide Dimethyl Acetals

inferredcites →https://doi.org/10.1021/ja0762994openalex-snapshot

Discovery and Mechanistic Study of AlIII-Catalyzed Transamidation of Tertiary Amides

inferredcites →https://doi.org/10.1021/ja0768136openalex-snapshot

N-Heterocyclic Carbene-Catalyzed Redox Amidations of α-Functionalized Aldehydes with Amines

inferredcites →https://doi.org/10.1021/ja2080086openalex-snapshot

Powerful Amide Synthesis from Alcohols and Amines under Aerobic Conditions Catalyzed by Gold or Gold/Iron, -Nickel or -Cobalt Nanoparticles

inferredcites →https://doi.org/10.1021/ja808129popenalex-snapshot

Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen

inferredcites →https://doi.org/10.1021/ja8094262openalex-snapshot

Catalytic Transamidation Reactions Compatible with Tertiary Amide Metathesis under Ambient Conditions

inferredcites →https://doi.org/10.1021/ja994280yopenalex-snapshot

Proline-Catalyzed Direct Asymmetric Aldol Reactions

inferredcites →https://doi.org/10.1021/jm200187yopenalex-snapshot

The Medicinal Chemist’s Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates

inferredcites →https://doi.org/10.1021/jo3008594openalex-snapshot

Proline Catalyzes Direct C–H Arylations of Unactivated Arenes

inferredcites →https://doi.org/10.1021/jo301252copenalex-snapshot

Copper-Catalyzed Oxidative Amidation of Aldehydes with Amine Salts: Synthesis of Primary, Secondary, and Tertiary Amides

inferredcites →https://doi.org/10.1021/jo3025303openalex-snapshot

Synthesis of Imidazo[1,2-a]pyridines: “Water-Mediated” Hydroamination and Silver-Catalyzed Aminooxygenation

inferredcites →https://doi.org/10.1021/jo9606564openalex-snapshot

3,4,5-Trifluorobenzeneboronic Acid as an Extremely Active Amidation Catalyst

inferredcites →https://doi.org/10.1021/ol0494459openalex-snapshot

Synthesis of Carboxamides by LDA-Catalyzed Haller−Bauer and Cannizzaro Reactions

inferredcites →https://doi.org/10.1021/ol102926nopenalex-snapshot

Brønsted Base-Assisted Boronic Acid Catalysis for the Dehydrative Intramolecular Condensation of Dicarboxylic Acids

inferredcites →https://doi.org/10.1021/ol301308copenalex-snapshot

Boric Acid: A Highly Efficient Catalyst for Transamidation of Carboxamides with Amines

inferredcites →https://doi.org/10.1021/ol900723vopenalex-snapshot

Ruthenium-Catalyzed Oxidation of Alcohols into Amides

inferredcites →https://doi.org/10.1021/om050768yopenalex-snapshot

Titanium(IV)-Mediated Conversion of Carboxamides to Amidines and Implications for Catalytic Transamidation

inferredcites →https://doi.org/10.1038/73200openalex-snapshot

In vivo antigen challenge in celiac disease identifies a single transglutaminase-modified peptide as the dominant A-gliadin T-cell epitope

inferredcites →https://doi.org/10.1038/nature07367openalex-snapshot

The advent and development of organocatalysis

inferredcites →https://doi.org/10.1038/nrd1133openalex-snapshot

Large-scale manufacture of peptide therapeutics by chemical synthesis

inferredcites →https://doi.org/10.1039/b701677hopenalex-snapshot

Amide bond formation: beyond the myth of coupling reagents

inferredcites →https://doi.org/10.1039/b902469gopenalex-snapshot

Supported silver nanoparticle catalyst for selective hydration of nitriles to amides in water

inferredcites →https://doi.org/10.1039/b903816gopenalex-snapshot

Organocatalysis—after the gold rush

inferredcites →https://doi.org/10.1039/b923093aopenalex-snapshot

The thermal and boron-catalysed direct amide formation reactions: mechanistically understudied yet important processes

inferredcites →https://doi.org/10.1039/c1cc15210fopenalex-snapshot

Direct amide formation from unactivated carboxylic acids and amines

inferredcites →https://doi.org/10.1039/c1ob05875dopenalex-snapshot

Copper-catalyzed synthesis of substituted indazoles from 2-chloroarenes at low catalyst-loading

inferredcites →https://doi.org/10.1039/c2cc37427gopenalex-snapshot

Transamidation of primary amides with amines catalyzed by zirconocene dichloride

inferredcites →https://doi.org/10.1039/c2gc16316kopenalex-snapshot

Transamidation of amides with amines under solvent-free conditions using a CeO2 catalyst

inferredcites →https://doi.org/10.1039/c2gc35765hopenalex-snapshot

l-Proline-promoted three-component reaction of anilines, aldehydes and barbituric acids/malononitrile: regioselective synthesis of 5-arylpyrimido[4,5-b]quinoline-diones and 2-amino-4-arylquinoline-3-carbonitriles in water

inferredcites →https://doi.org/10.1039/c2ra22459copenalex-snapshot

Hypervalent iodine catalyzed transamidation of carboxamides with amines

inferredcites →https://doi.org/10.1071/ch11301openalex-snapshot

Intramolecular Dehydrative Condensation of Dicarboxylic Acids with Brønsted Base-Assisted Boronic Acid Catalysts

inferredcites →https://doi.org/10.1073/pnas.93.25.14310openalex-snapshot

Neurodegenerative diseases and transglutaminase

inferredcites →https://doi.org/10.1126/science.1145295openalex-snapshot

Direct Synthesis of Amides from Alcohols and Amines with Liberation of H 2

inferredcites →https://doi.org/10.3987/rev-07-621openalex-snapshot

Organocatalytic Asymmetric Synthesis Using Proline and Related Molecules. Part 2.

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.4096979openalex-extracted

The Synthesis of Amides Under Catalyst-Free Conditions

inferred← citeshttps://doi.org/10.1002/047084289x.rn01754openalex-snapshot

Tris(2,2,2-trifluoroethoxy)boron

inferred← citeshttps://doi.org/10.1002/9780471264194.fos11713openalex-snapshot

( S )‐Proline and 4‐hydroxyproline

inferred← citeshttps://doi.org/10.1002/9780471264194.fos12157.pub2openalex-snapshot

( S/R )‐Proline and 4‐hydroxyproline

inferred← citeshttps://doi.org/10.1002/9781118707838.ch2openalex-snapshot

Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and Their Derivatives

inferred← citeshttps://doi.org/10.1002/9781118905074.ch05openalex-snapshot

Protection for the Carboxyl Group

inferred← citeshttps://doi.org/10.1002/9783527651733.ch27openalex-snapshot

Catalytic Amide Bond Forming Methods

inferred← citeshttps://doi.org/10.1002/9783527830251.ch6openalex-snapshot

Transamidation of Carboxamides and Amide Derivatives: Mechanistic Insights, Concepts, and Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201300717openalex-snapshot

Mesoporous Niobium Oxide Spheres as an Effective Catalyst for the Transamidation of Primary Amides with Amines

inferred← citeshttps://doi.org/10.1002/adsc.201400068openalex-snapshot

Benzoic Acid‐Catalyzed Transamidation Reactions of Carboxamides, Phthalimide, Ureas and Thioamide with Amines

inferred← citeshttps://doi.org/10.1002/adsc.201400319openalex-snapshot

Tandem Synthesis of Amides and Secondary Amines from Esters with Primary Amines under Solvent‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.201600373openalex-snapshot

An Efficient Heterobimetallic Lanthanide Alkoxide Catalyst for Transamidation of Amides under Solvent‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.201801673openalex-snapshot

Graphene Oxide: A Metal‐Free Carbocatalyst for the Synthesis of Diverse Amides under Solvent‐Free Conditions

inferred← citeshttps://doi.org/10.1002/adsc.202300984openalex-snapshot

Molecular Oxygen‐Induced Transamidation of Unactivated Amides in Diethyl Carbonate in the Presence of a Palladium Catalyst

inferred← citeshttps://doi.org/10.1002/ajoc.201900216openalex-snapshot

Metal‐Free Transamidation of Primary Amides using Trimethylsilyl Chloride

inferred← citeshttps://doi.org/10.1002/ajoc.202200076openalex-snapshot

Synthesis of N‐Cbz Amides and Their Applications in the Transamidation Reactions at Room Temperature

inferred← citeshttps://doi.org/10.1002/ajoc.202200378openalex-snapshot

Environmentally Benign Transamidation Protocol for Weakly Nucleophilic Aromatic Amines with N‐Acyl‐2‐piperidinones: Catalyst‐, Additive‐, Base‐ and Solvent‐Free Condition

inferred← citeshttps://doi.org/10.1002/ange.201803797openalex-snapshot

Katalytische, isofunktionelle Reaktionen – Erweiterung des Repertoires an Shuttle‐ und Metathesereaktionen

inferred← citeshttps://doi.org/10.1002/ange.201810548openalex-snapshot

Copper‐Catalyzed Transsulfinamidation of Sulfinamides as a Key Step in the Preparation of Sulfonamides and Sulfonimidamides

inferred← citeshttps://doi.org/10.1002/ange.202202794openalex-snapshot

Highly Chemoselective Transamidation of Unactivated Tertiary Amides by Electrophilic N−C(O) Activation by Amide‐to‐Acyl Iodide Re‐routing

inferred← citeshttps://doi.org/10.1002/anie.201803797openalex-snapshot

Catalytic Isofunctional Reactions—Expanding the Repertoire of Shuttle and Metathesis Reactions

inferred← citeshttps://doi.org/10.1002/anie.201810548openalex-snapshot

Copper‐Catalyzed Transsulfinamidation of Sulfinamides as a Key Step in the Preparation of Sulfonamides and Sulfonimidamides

inferred← citeshttps://doi.org/10.1002/anie.202202794openalex-snapshot

Highly Chemoselective Transamidation of Unactivated Tertiary Amides by Electrophilic N−C(O) Activation by Amide‐to‐Acyl Iodide Re‐routing

inferred← citeshttps://doi.org/10.1002/asia.202101308openalex-snapshot

A Comparison of Immobilised Triphenylphosphine and 1‐Hydroxybenzotriazole as Mediators of Catch‐and‐Release Acylation Under Flow Conditions

inferred← citeshttps://doi.org/10.1002/asia.202500327openalex-snapshot

Advances in Metal‐Free Transamidation: A Sustainable Approach to Amide Bond Formation

inferred← citeshttps://doi.org/10.1002/bkcs.12371openalex-snapshot

Amides Activation: Transition Metal‐Free Coupling Between CN Activated Amides and Enolizable Amides

inferred← citeshttps://doi.org/10.1002/cctc.201800609openalex-snapshot

Copper‐(II) Catalyzed N‐Formylation and N‐Acylation of Aromatic, Aliphatic, and Heterocyclic Amines and a Preventive Study in the C‐N Cross Coupling of Amines with Aryl Halides

inferred← citeshttps://doi.org/10.1002/chem.201600234openalex-snapshot

Formamide Synthesis through Borinic Acid Catalysed Transamidation under Mild Conditions

inferred← citeshttps://doi.org/10.1002/chin.201333042openalex-snapshot

ChemInform Abstract: L‐Proline: An Efficient Catalyst for Transamidation of Carboxamides with Amines.

inferred← citeshttps://doi.org/10.1002/cssc.201500318openalex-snapshot

CN and NH Bond Metathesis Reactions Mediated by Carbon Dioxide

inferred← citeshttps://doi.org/10.1002/ejoc.201300573openalex-snapshot

Recent Developments in Amide Synthesis: Direct Amidation of Carboxylic Acids and Transamidation Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.201402386openalex-snapshot

Trimethylaluminium‐Mediated Reaction of Primary Carboxamides with Amines and Indoles: A Convenient Synthesis of Amidines and Indole‐3‐acylimines

inferred← citeshttps://doi.org/10.1002/ejoc.201500616openalex-snapshot

Construction of Diverse and Functionalized 2H‐Chromenes by Organocatalytic Multicomponent Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.201601625openalex-snapshot

An Unconventional Reaction of 2,2‐Diazido Acylacetates with Amines

inferred← citeshttps://doi.org/10.1002/ejoc.201800253openalex-snapshot

Cobalt(II)‐Catalyzed N‐Acylation of Amines through a Transamidation Reaction

inferred← citeshttps://doi.org/10.1002/ejoc.201900517openalex-snapshot

Mild, Metal‐Free and Protection‐Free Transamidation of N‐Acyl‐2‐piperidones to Amino Acids, Amino Alcohols and Aliphatic Amines and Esterification of N‐Acyl‐2‐piperidones

inferred← citeshttps://doi.org/10.1002/ejoc.202000467openalex-snapshot

Polyethylene Glycol (PEG‐400) as Methylene Spacer and Green Solvent for the Synthesis of Heterodiarylmethanes under Metal‐Free Conditions

inferred← citeshttps://doi.org/10.1002/ejoc.202101135openalex-snapshot

Ionic‐Liquid‐Catalyzed Synthesis of Imines, Benzimidazoles, Benzothiazoles, Quinoxalines and Quinolines through C−N, C−S, and C−C Bond Formation

inferred← citeshttps://doi.org/10.1002/ejoc.202300930openalex-snapshot

Molecular Construction Using Formamide as a C1 Feedstock

inferred← citeshttps://doi.org/10.1002/hc.21321openalex-snapshot

Effective Synthesis of N‐Arylformamide from α‐Halo‐N‐arylacetamides

inferred← citeshttps://doi.org/10.1002/slct.201601433openalex-snapshot

Guanidine Acetic Acid Functionalized Magnetic Nanoparticles: Recoverable Green Catalyst for Transamidation

inferred← citeshttps://doi.org/10.1002/slct.201701250openalex-snapshot

Oxidative Amidation of Methylarenes and Heteroamines under Metal‐Free Conditions

inferred← citeshttps://doi.org/10.1002/slct.202000764openalex-snapshot

Recent Advances in the Protection of Amine Functionality: A Review

inferred← citeshttps://doi.org/10.1002/slct.202302159openalex-snapshot

Water‐Mediated C−H Cyanation of Quinoxalin‐2(1 H )‐ones and Quinoxalines Under Visible‐Light Conditions

inferred← citeshttps://doi.org/10.1002/slct.202303345openalex-snapshot

Mechanism of Hydroxylamine Hydrochloride‐Catalyzed Transamidation: Covalent Catalysis over Hydrogen Bonding

inferred← citeshttps://doi.org/10.1007/s11051-018-4195-5openalex-snapshot

Mesoporous silica nanoparticles in an efficient solvent-free transamidation of carboxamides with amines: an exhibition of a green recyclable nanocatalyst

inferred← citeshttps://doi.org/10.1007/s11164-015-2133-zopenalex-snapshot

Reusable proline-based ionic liquid catalyst for the simple synthesis of 2-arylbenzothiazoles in a biomass medium

inferred← citeshttps://doi.org/10.1007/s11164-016-2588-6openalex-snapshot

A green organocatalyzed one-pot protocol for efficient synthesis of new substituted pyrimido[4,5-d]pyrimidinones using a Biginelli-like reaction

inferred← citeshttps://doi.org/10.1007/s11696-023-02772-wopenalex-snapshot

Recent advances in transamidation of unactivated amides

inferred← citeshttps://doi.org/10.1007/s12039-023-02189-8openalex-snapshot

L-Proline assisted expeditious and efficient methodology for the preparation of 2-amino-3-cyanopyridines under aqueous conditions

inferred← citeshttps://doi.org/10.1007/s13738-018-1471-3openalex-snapshot

N-formylation of amine using graphene oxide as a sole recyclable metal-free carbocatalyst

inferred← citeshttps://doi.org/10.1007/s13738-018-1523-8openalex-snapshot

Citric acid stabilized on the surface of magnetic nanoparticles as an efficient and recyclable catalyst for transamidation of carboxamides, phthalimide, urea and thiourea with amines under neat conditions

inferred← citeshttps://doi.org/10.1016/b978-0-323-95893-6.00001-3openalex-snapshot

Visible light–driven organic synthesis under Rose Bengal photocatalysis

inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00106-xopenalex-snapshot

N-Acylation Reactions of Amines

inferred← citeshttps://doi.org/10.1016/j.apcata.2015.01.014openalex-snapshot

Designing of thermally stable amide functionalized benzimidazolium perchlorate ionic liquid for transamidation of primary carboxamides

inferred← citeshttps://doi.org/10.1016/j.apcata.2020.117842openalex-snapshot

Surface wettability modification of amine-functionalized polyacrylonitrile fiber to enhance heterogeneous catalytic performance for aldol reaction in water

inferred← citeshttps://doi.org/10.1016/j.bios.2021.113493openalex-snapshot

A chemical-enhanced system for CRISPR-Based nucleic acid detection

inferred← citeshttps://doi.org/10.1016/j.catcom.2016.04.004openalex-snapshot

Transamidation of carboxamides with amines over nanosized zeolite beta under solvent-free conditions

inferred← citeshttps://doi.org/10.1016/j.gresc.2024.11.008openalex-snapshot

TFA-catalyzed cascade annulation of thioamides with aromatic hydrazides/amines: An internal oxidant-triggered protocol to diverse N-heterocycles

inferred← citeshttps://doi.org/10.1016/j.ica.2025.122936openalex-snapshot

Transamidation of carboxamides with amines – An intramolecular CN cleavage/CN coupling reaction catalyzed by Ruthenium(II) complexes based on isonicotinichydrazones

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2024.110328openalex-snapshot

Potassium hexafluorotitanate as a catalytic activator for direct amidation of carboxylic acids

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121359openalex-snapshot

A novel gold(I)-mediated intramolecular transamidation of benzoyl thiourea derivatives to form benzamides via dethiocyanation

inferred← citeshttps://doi.org/10.1016/j.molcata.2015.03.015openalex-snapshot

An attractive route to transamidation catalysis: Facile synthesis of new o-aryloxide-N-heterocyclic carbene ruthenium(II) complexes containing trans triphenylphosphine donors

inferred← citeshttps://doi.org/10.1016/j.snb.2016.10.041openalex-snapshot

Lab-on-a-Molecule elaboration for fluorescence based discrimination of commercial surfactants sodium dodecyl sulfate and sodium dodecylbenzenesulfonate

inferred← citeshttps://doi.org/10.1016/j.tet.2014.10.066openalex-snapshot

Microwave-assisted heteropolyanion-based ionic liquids catalyzed transamidation of non-activated carboxamides with amines under solvent-free conditions

inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.071openalex-snapshot

N-Heterocyclic carbene-catalysed amidation of vinyl esters with aromatic amines

inferred← citeshttps://doi.org/10.1016/j.tet.2015.06.066openalex-snapshot

Zirconium-catalyzed direct amide bond formation between carboxylic esters and amines

inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.008openalex-snapshot

Synthesis of N-arylcarboxamides by the efficient transamidation of DMF and derivatives with anilines

inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.016openalex-snapshot

Efficient conversion of acids and esters to amides and transamidation of primary amides using OSU-6

inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.060openalex-snapshot

AIBN-promoted amidation of anilines with 1, 3-diketones via oxidative cleavage of C–C bond under aerobic conditions

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.066openalex-snapshot

Synthesis and evaluation of some variants of the Nefkens’ reagent

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.112openalex-snapshot

Water mediated deprotective intramolecular hydroamination of N-propargylaminopyridines: synthesis of imidazo[1,2-a]pyridines

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.11.029openalex-snapshot

Formylation of amines through catalyst- and solvent-free transamidation reaction

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.111openalex-snapshot

Fe3+-exchanged clay catalyzed transamidation of amides with amines under solvent-free condition

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.01.046openalex-snapshot

Ligand free open air copper(II) mediated aryl formamidation and amination of aryl halides

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.07.083openalex-snapshot

Oxidative synthesis of benzamides from toluenes and DMF

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.052openalex-snapshot

A metal-free approach for transamidation of amides with amines in aqueous media

inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.01.056openalex-snapshot

Tetraethylorthosilicate as a mild dehydrating reagent for the synthesis of N-formamides with formic acid

inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.01.060openalex-snapshot

Graphene oxide (GO) catalyzed transamidation of aliphatic amides: An efficient metal-free procedure

inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.03.071openalex-snapshot

An efficient method for the N-formylation of amines under catalyst- and additive-free conditions

inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152195openalex-snapshot

A KHSO4 promoted tandem synthesis of 1,3,4-thiadiazoles from thiohydrazides and DMF derivatives

inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154312openalex-snapshot

Practical povidone iodine catalyzed transamidation from primary amides and amines

inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154392openalex-snapshot

Direct synthesis of amides through transamidation using dichloroimidazolinedione (DCID)

inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156273openalex-snapshot

Base mediated [3+2] annulations of α-chlorohydroxamates with 1,3-disubstituted-thioureas via nucleophilic substitution-transamidation reaction

inferred← citeshttps://doi.org/10.1021/acs.joc.1c02077openalex-snapshot

A CO 2 -Catalyzed Transamidation Reaction

inferred← citeshttps://doi.org/10.1021/acs.joc.3c02352openalex-snapshot

Direct Transamidation of Thioamides with Amines via Acetophenone-Promoted Enamine Catalysis under Metal-Free Conditions

inferred← citeshttps://doi.org/10.1021/acs.joc.5b01173openalex-snapshot

Synthesis of the Core Tricyclic Ring Domain of (−)-Schulzeine B

inferred← citeshttps://doi.org/10.1021/acs.joc.5c00148openalex-snapshot

Denitrogenative Radical Transacetylation of Amines Using Acetohydrazide in Water at Room Temperature

inferred← citeshttps://doi.org/10.1021/acs.joc.5c01647openalex-snapshot

Mechanochemical Unlocking of Phthalimide Transamidation: A Path to N-Substituted Phthalamides

inferred← citeshttps://doi.org/10.1021/acs.joc.7b00002openalex-snapshot

Copper Catalyzed C–N Cross-Coupling Reaction of Aryl Boronic Acids at Room Temperature through Chelation Assistance

inferred← citeshttps://doi.org/10.1021/acs.joc.7b02211openalex-snapshot

I2-Catalyzed Oxidative Amidation of Benzylamines and Benzyl Cyanides under Mild Conditions

inferred← citeshttps://doi.org/10.1021/acs.joc.8b00128openalex-snapshot

Synthesis of 2-Aminopyridines via a Base-Promoted Cascade Reaction of N -Propargylic β-Enaminones with Formamides

inferred← citeshttps://doi.org/10.1021/acs.joc.9b01777openalex-snapshot

Metal-Free C–N or C–C Bond Cleavages of α-Azido Ketones: An Oxidative-Amidation Strategy for the Synthesis of α-Ketothioamides and Amides

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00485openalex-snapshot

Nickel-Catalyzed Claisen Condensation Reaction between Two Different Amides

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00958openalex-snapshot

Transamidation for the Synthesis of Primary Amides at Room Temperature

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03870openalex-snapshot

K2S2O8-Mediated Denitrogenative Formal Transformylation of Amines with Formylhydrazine in Water

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02913openalex-snapshot

Dioxygen-Promoted Pd-Catalyzed Aminocarbonylation of Organoboronic Acids with Amines and CO: A Direct Approach to Tertiary Amides

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00796openalex-snapshot

A General Method for Two-Step Transamidation of Secondary Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (N-Heterocyclic Carbene) Complexes

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02303openalex-snapshot

Intramolecular Transamidation of Secondary Amides via Visible-Light-Induced Tandem Reaction

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03542openalex-snapshot

Catalyst-Free Transamidation of Aromatic Amines with Formamide Derivatives and Tertiary Amides with Aliphatic Amines

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02306openalex-snapshot

KOtBu-Promoted Transition-Metal-Free Transamidation of Primary and Tertiary Amides with Amines

inferred← citeshttps://doi.org/10.1021/acscatal.9b05074openalex-snapshot

Zn-Catalyzed Nicotinate-Directed Transamidations in Peptide Synthesis

inferred← citeshttps://doi.org/10.1021/jo400509nopenalex-snapshot

Direct Synthesis of Amides from Carboxylic Acids and Amines Using B(OCH 2 CF 3 ) 3

inferred← citeshttps://doi.org/10.1021/jo400834hopenalex-snapshot

Sodium Hydroxide Catalyzed N-Alkylation of (Hetero) Aromatic Primary Amines and N1,C5-Dialkylation of 4-Phenyl-2-aminothiazoles with Benzyl Alcohols

inferred← citeshttps://doi.org/10.1021/jo500562wopenalex-snapshot

Transamidation of Carboxamides Catalyzed by Fe(III) and Water

inferred← citeshttps://doi.org/10.1021/ol4023886openalex-snapshot

MnO2 Promoted Sequential C–O and C–N Bond Formation via C–H Activation of Methylarenes: A New Approach to Amides

inferred← citeshttps://doi.org/10.1038/s41598-019-39210-5openalex-snapshot

MoS2-Catalyzed transamidation reaction

inferred← citeshttps://doi.org/10.1038/s41598-024-57608-8openalex-snapshot

Direct additive-free N-formylation and N-acylation of anilines and synthesis of urea derivatives using green, efficient, and reusable deep eutectic solvent ([ChCl][ZnCl2]2)

inferred← citeshttps://doi.org/10.1039/c3ra45176copenalex-snapshot

A binuclear Mn( ii ) complex as an efficient catalyst for transamidation of carboxamides with amines

inferred← citeshttps://doi.org/10.1039/c4cc08503eopenalex-snapshot

A phthalimidation protocol that follows protein defined parameters

inferred← citeshttps://doi.org/10.1039/c4cc09940kopenalex-snapshot

Copper catalysed amidation of aryl halides through chelation assistance

inferred← citeshttps://doi.org/10.1039/c4gc01402bopenalex-snapshot

Chitosan: an efficient recyclable catalyst for transamidation of carboxamides with amines under neat conditions

inferred← citeshttps://doi.org/10.1039/c4ob01931hopenalex-snapshot

Oxidative activation of dihydropyridine amides to reactive acyl donors

inferred← citeshttps://doi.org/10.1039/c4ra04105dopenalex-snapshot

Mechanistic insights into l -proline-catalyzed transamidation of carboxamide with benzylamine from density functional theory calculations

inferred← citeshttps://doi.org/10.1039/c4ra09065aopenalex-snapshot

Ammonolysis of anilides promoted by ethylene glycol and phosphoric acid

inferred← citeshttps://doi.org/10.1039/c4ra09091hopenalex-snapshot

Microwave assisted chemoselective organocatalytic peptide alcohol synthesis from C-terminal amide

inferred← citeshttps://doi.org/10.1039/c4ra15140bopenalex-snapshot

Copper catalysed C–N bond formation via a sequential acylation and deacylation process: a novel strategy for the synthesis of benzanilides

inferred← citeshttps://doi.org/10.1039/c4ra16571copenalex-snapshot

Sulphuric acid immobilized on silica gel (H 2 SO 4 –SiO 2 ) as an eco-friendly catalyst for transamidation

inferred← citeshttps://doi.org/10.1039/c5cc00623fopenalex-snapshot

Organocatalyzed benzannulation for the construction of diverse anthraquinones and tetracenediones

inferred← citeshttps://doi.org/10.1039/c5ra13094hopenalex-snapshot

MnO 2 catalyzed formylation of amines and transamidation of amides under solvent-free conditions

inferred← citeshttps://doi.org/10.1039/c5ra13708jopenalex-snapshot

Metal-free C–N cross-coupling of electrophilic compounds and N-haloimides

inferred← citeshttps://doi.org/10.1039/c5ra16933jopenalex-snapshot

H-β-zeolite catalyzed transamidation of carboxamides, phthalimide, formamides and thioamides with amines under neat conditions

inferred← citeshttps://doi.org/10.1039/c5ra21932aopenalex-snapshot

Reactant cum solvent water: generation of transient λ 3 -hypervalent iodine, its reactivity, mechanism and broad application

inferred← citeshttps://doi.org/10.1039/c5ra27680bopenalex-snapshot

Transamidation of primary carboxamides, phthalimide, urea and thiourea with amines using Fe(OH) 3 @Fe 3 O 4 magnetic nanoparticles as an efficient recyclable catalyst

inferred← citeshttps://doi.org/10.1039/c6gc02603fopenalex-snapshot

Ru/ceria-catalyzed direct formylation of amines and CO to produce formamides

inferred← citeshttps://doi.org/10.1039/c6ra11784hopenalex-snapshot

Two catalytic systems of l -proline/Cu( ii ) catalyzed allylic oxidation of olefins with tert-butyl hydroperoxide

inferred← citeshttps://doi.org/10.1039/c7cp05474bopenalex-snapshot

Investigation of the dynamics of aqueous proline solutions using neutron scattering and molecular dynamics simulations

inferred← citeshttps://doi.org/10.1039/c7ob02874aopenalex-snapshot

Transamidation of N -acyl-glutarimides with amines

inferred← citeshttps://doi.org/10.1039/c7ra12152kopenalex-snapshot

Fe-catalyzed esterification of amides via C–N bond activation

inferred← citeshttps://doi.org/10.1039/c7sc01980gopenalex-snapshot

Nickel-catalyzed transamidation of aliphatic amide derivatives

inferred← citeshttps://doi.org/10.1039/c8gc03726dopenalex-snapshot

Ionic liquid catalysed aerobic oxidative amidation and thioamidation of benzylic amines under neat conditions

inferred← citeshttps://doi.org/10.1039/c8ob03010copenalex-snapshot

tert -Butyl nitrite promoted transamidation of secondary amides under metal and catalyst free conditions

inferred← citeshttps://doi.org/10.1039/c9ob02096aopenalex-snapshot

Solvent- and catalyst-free transamidations of unprotected glycosyl carboxamides

inferred← citeshttps://doi.org/10.1039/d0gc02168gopenalex-snapshot

Visible-light induced phosphonation of quinoxalines and quinoxalin-2(1 H )-ones under aerobic metal-free conditions

inferred← citeshttps://doi.org/10.1039/d0ob01271hopenalex-snapshot

Nickel/briphos-catalyzed transamidation of unactivated tertiary amides

inferred← citeshttps://doi.org/10.1039/d0qo00797hopenalex-snapshot

Coupling of amides with ketones via C–N/C–H bond cleavage: a mild synthesis of 1,3-diketones

inferred← citeshttps://doi.org/10.1039/d1ra04848aopenalex-snapshot

Catalyst free N -formylation of aromatic and aliphatic amines exploiting reductive formylation of CO 2 using NaBH 4

inferred← citeshttps://doi.org/10.1039/d1ra09327dopenalex-snapshot

Innovative application of magnetically modified bovine horn as a natural keratin resource in the role of value-added organocatalyst

inferred← citeshttps://doi.org/10.1039/d2ob00882copenalex-snapshot

Transamidation of aromatic amines with formamides using cyclic dihydrogen tetrametaphosphate

inferred← citeshttps://doi.org/10.1039/d3ob01728aopenalex-snapshot

Reductive transamidation of tertiary amides with nitroarenes enabled by magnesium and chlorosilane

inferred← citeshttps://doi.org/10.1039/d3qo00571bopenalex-snapshot

The metal- and column-free synthesis of pyridin-2-yl ureas carrying cyclic secondary amine substituents and establishing the mechanism of the reactions through a computational study

inferred← citeshttps://doi.org/10.1055/a-2388-9578openalex-snapshot

Sustainable N-Formylation of Anilines: Harnessing Aleuritic Acid as a Renewable Formyl Source

inferred← citeshttps://doi.org/10.1055/s-0040-1707133openalex-snapshot

Amide Synthesis by Transamidation of Primary Carboxamides

inferred← citeshttps://doi.org/10.1080/00304948.2021.1908047openalex-snapshot

Solvent-free, Efficient Transamidation of Carboxamides with Amines Catalyzed by Recyclable Sulfated Polyborate Catalyst

inferred← citeshttps://doi.org/10.1080/00304948.2023.2259771openalex-snapshot

Sulfated Starch: A Highly Efficient Catalyst for Transamidation of Primary and Secondary Amines with Formamide and Acetamide

inferred← citeshttps://doi.org/10.1080/00397911.2023.2228947openalex-snapshot

Electrochemical oxidative transamidation of tertiary amines with N -acyl imides to access amide compounds

inferred← citeshttps://doi.org/10.1080/10406638.2019.1686401openalex-snapshot

One-Pot Assembly for Synthesis of 1,4-Dihydropyridine Scaffold and Their Biological Applications

inferred← citeshttps://doi.org/10.1080/10406638.2023.2257841openalex-snapshot

Metal- and Hazardous Reagent-Free Transamidation Process: the NH 2 OH⦁HCl Promoted N -Formylation and N -Acylation Reaction under Solvent-Less Conditions

inferred← citeshttps://doi.org/10.1080/17518253.2018.1528389openalex-snapshot

γ-aminobutyric acid and collagen peptides as recyclable bifunctional biocatalysts for the solvent-free one-pot synthesis of 2-aminobenzothiazolomethyl-2-naphthols

inferred← citeshttps://doi.org/10.1107/s2053229615019828openalex-snapshot

Crystal structures of the pyrazinamide–p-aminobenzoic acid (1/1) cocrystal and the transamidation reaction product 4-(pyrazine-2-carboxamido)benzoic acid in the molten state

inferred← citeshttps://doi.org/10.1134/s1070363215040088openalex-snapshot

Colloid and nano-sized catalysts in organic synthesis: X. Synthesis of carboxamides by direct amidation of carboxylic acids and transamidation catalyzed by colloid copper

inferred← citeshttps://doi.org/10.1515/chempap-2015-0168openalex-snapshot

Ce(III) immobilised on aminated epichlorohydrin-activated agarose matrix – “green” and efficient catalyst for transamidation of carboxamides

inferred← citeshttps://doi.org/10.2174/1570178619666220928152249openalex-snapshot

The Synthesis of Amides from Benzoic Acids and Dicarbodiimides Under Catalyst-Free Conditions

inferred← citeshttps://doi.org/10.2174/2213337207999201117093848openalex-snapshot

Amino Acids and Peptides Organocatalysts: A Brief Overview on Its Evolution and Applications in Organic Asymmetric Synthesis

inferred← citeshttps://doi.org/10.26434/chemrxiv.13087730openalex-snapshot

A New Method for Transcarbamation and Amidation from Benzyl Carbamate

inferred← citeshttps://doi.org/10.26434/chemrxiv.13087730.v1openalex-snapshot

A New Method for Transcarbamation and Amidation from Benzyl Carbamate

inferred← citeshttps://doi.org/10.3390/catal9020129openalex-snapshot

N-Acylphthalimides: Efficient Acyl Coupling Reagents in Suzuki–Miyaura Cross-Coupling by N–C Cleavage Catalyzed by Pd–PEPPSI Precatalysts

inferred← citeshttps://doi.org/10.3390/molecules23092234openalex-snapshot

Imidazolium Chloride: An Efficient Catalyst for Transamidation of Primary Amines

inferred← citeshttps://doi.org/10.3390/molecules23092382openalex-snapshot

Direct Transamidation Reactions: Mechanism and Recent Advances

inferred← citeshttps://doi.org/10.3390/molecules26216374openalex-snapshot

A Journey from June 2018 to October 2021 with N,N-Dimethylformamide and N,N-Dimethylacetamide as Reactants

inferred← citeshttps://doi.org/10.3390/suschem4010001openalex-snapshot

Recovery of Lac Resin from the Aqueous Effluent of Shellac Industry

inferred← citeshttps://doi.org/10.3762/bjoc.11.240openalex-snapshot

Recent advances in copper-catalyzed C–H bond amidation

inferred← citeshttps://doi.org/10.3987/com-13-s(s)41openalex-snapshot

Hydrogen Bond Organocatalysis of Benzotriazole in Transamidation of Carboxamides with Amines

inferred← citeshttps://doi.org/10.4172/2167-7956.1000140openalex-snapshot

L-Proline: An Efficient and Selective Catalyst for Transamidation of Thioamides with Amines

inferred← citeshttps://doi.org/10.5012/bkcs.2014.35.9.2673openalex-snapshot

Theoretical Insight into the Mechanism of an Efficient ʟ-Proline-catalyzed Transamidation of Acetamide with Benzylamine

inferred← citeshttps://doi.org/10.6023/cjoc202010010openalex-snapshot

Lactic Acid-Catalyzed Transamidation Reactions of Carboxamides with Amines

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.