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Recent Developments in Amide Synthesis: Direct Amidation of Carboxylic Acids and Transamidation Reactions
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.200705468openalex-snapshot
Direct and Waste‐Free Amidations and Cycloadditions by Organocatalytic Activation of Carboxylic Acids at Room Temperature
inferredcites →https://doi.org/10.1002/ange.201003188openalex-snapshot
Mechanistic Insights into Direct Amide Bond Formation Catalyzed by Boronic Acids: Halogens as Lewis Bases
inferredcites →https://doi.org/10.1002/ange.201107348openalex-snapshot
Transamidation of Primary Amides with Amines Using Hydroxylamine Hydrochloride as an Inorganic Catalyst
inferredcites →https://doi.org/10.1002/ange.201108599openalex-snapshot
Efficient Copper(II)‐Catalyzed Transamidation of Non‐Activated Primary Carboxamides and Ureas with Amines
inferredcites →https://doi.org/10.1002/chem.201104055openalex-snapshot
Direct Amide Coupling of Non‐activated Carboxylic Acids and Amines Catalysed by Zirconium(IV) Chloride
inferredcites →https://doi.org/10.1002/ejoc.200901420openalex-snapshot
Simple Synthesis of Amides and Weinreb Amides Using PPh3 or Polymer‐Supported PPh3 and Iodine
inferredcites →https://doi.org/10.1002/ejoc.201100714openalex-snapshot
The Uncatalyzed Direct Amide Formation Reaction – Mechanism Studies and the Key Role of Carboxylic Acid H‐Bonding
inferredcites →https://doi.org/10.1016/j.tet.2005.08.031openalex-snapshot
Amide bond formation and peptide coupling
inferredcites →https://doi.org/10.1016/j.tet.2008.09.094openalex-snapshot
Carboxamidation of carboxylic acids with 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) without bases
inferredcites →https://doi.org/10.1016/j.tet.2008.11.004openalex-snapshot
Dehydrative condensation catalyses
inferredcites →https://doi.org/10.1016/s0040-4020(01)92983-7openalex-snapshot
Some amide forming reactions involving boron reagents
inferredcites →https://doi.org/10.1016/s0040-4039(00)99121-4openalex-snapshot
A convenient synthesis of amides from carboxylic acids and primary amines
inferredcites →https://doi.org/10.1021/cc9800071openalex-snapshot
A Knowledge-Based Approach in Designing Combinatorial or Medicinal Chemistry Libraries for Drug Discovery. 1. A Qualitative and Quantitative Characterization of Known Drug Databases
inferredcites →https://doi.org/10.1021/ja00096a017openalex-snapshot
Boron Heterocycles Bearing a Peripheral Resemblance to Naturally-Occurring Purines: Design, Syntheses, Structures, and Properties
inferredcites →https://doi.org/10.1021/ja01286a013openalex-snapshot
Organic Reactions with Boron Fluoride. XIV. The Reaction of Amides with Acids and Amines1
inferredcites →https://doi.org/10.1021/ja01495a013openalex-snapshot
Synthesis of Aromatic Diboronic Acids1
inferredcites →https://doi.org/10.1021/ja028242hopenalex-snapshot
Catalytic Transamidation under Moderate Conditions
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/jo00094a004openalex-snapshot
Aluminum Chloride-Promoted Transamidation Reactions
inferredcites →https://doi.org/10.1021/jo00416a040openalex-snapshot
A new synthesis of amides and macrocyclic lactams
inferredcites →https://doi.org/10.1021/jo3013258openalex-snapshot
Direct Amidation of Carboxylic Acids Catalyzed by ortho-Iodo Arylboronic Acids: Catalyst Optimization, Scope, and Preliminary Mechanistic Study Supporting a Peculiar Halogen Acceleration Effect
inferredcites →https://doi.org/10.1021/jo400509nopenalex-snapshot
Direct Synthesis of Amides from Carboxylic Acids and Amines Using B(OCH 2 CF 3 ) 3
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/ol052060lopenalex-snapshot
N-Alkyl-4-boronopyridinium Salts as Thermally Stable and Reusable Amide Condensation Catalysts
inferredcites →https://doi.org/10.1021/ol060216ropenalex-snapshot
4,5,6,7-Tetrachlorobenzo[d][1,3,2]dioxaborol- 2-ol as an Effective Catalyst for the Amide Condensation of Sterically Demanding Carboxylic Acids
inferredcites →https://doi.org/10.1021/ol203007sopenalex-snapshot
AlMe3-Promoted Formation of Amides from Acids and Amines
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/ol400045dopenalex-snapshot
XtalFluor-E, an Efficient Coupling Reagent for Amidation of Carboxylic Acids
inferredcites →https://doi.org/10.1021/ol4002625openalex-snapshot
l -Proline: An Efficient Catalyst for Transamidation of Carboxamides with Amines
inferredcites →https://doi.org/10.1021/op1003105openalex-snapshot
Green Chemistry Articles of Interest to the Pharmaceutical Industry
inferredcites →https://doi.org/10.1021/op300068dopenalex-snapshot
Green Chemistry Articles of Interest to the Pharmaceutical Industry
inferredcites →https://doi.org/10.1021/op4000434openalex-snapshot
Green Chemistry Articles of Interest to the Pharmaceutical Industry
inferredcites →https://doi.org/10.1021/op700098wopenalex-snapshot
Boric Acid Catalyzed Amidation in the Synthesis of Active Pharmaceutical Ingredients
inferredcites →https://doi.org/10.1021/op900295sopenalex-snapshot
Green Chemistry Articles of Interest to the Pharmaceutical Industry
inferredcites →https://doi.org/10.1039/b602413kopenalex-snapshot
Analysis of the reactions used for the preparation of drug candidate molecules
inferredcites →https://doi.org/10.1039/b701677hopenalex-snapshot
Amide bond formation: beyond the myth of coupling reagents
inferredcites →https://doi.org/10.1039/b703488copenalex-snapshot
Key green chemistry research areas—a perspective from pharmaceutical manufacturers
inferredcites →https://doi.org/10.1039/b711717eopenalex-snapshot
Green chemistry tools to influence a medicinal chemistry and research chemistry based organisation
inferredcites →https://doi.org/10.1039/b712008gopenalex-snapshot
Synthesis, evaluation and application of novel bifunctional N,N-di-isopropylbenzylamineboronic acid catalysts for direct amide formation between carboxylic acids and amines
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/c0cs00196aopenalex-snapshot
Metal-catalysed approaches to amide bond formation
inferredcites →https://doi.org/10.1039/c0gc00053aopenalex-snapshot
Sulfated tungstate: a new solid heterogeneous catalyst for amide synthesis
inferredcites →https://doi.org/10.1039/c0ob01069copenalex-snapshot
Borate esters as convenient reagents for direct amidation of carboxylic acids and transamidation of primary amides
inferredcites →https://doi.org/10.1039/c1cc15210fopenalex-snapshot
Direct amide formation from unactivated carboxylic acids and amines
inferredcites →https://doi.org/10.1039/c2cc32153jopenalex-snapshot
Sodium methoxide: a simple but highly efficient catalyst for the direct amidation of esters
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/c2gc35037hopenalex-snapshot
Preparation of amides mediated by isopropylmagnesium chloride under continuous flow conditions
inferredcites →https://doi.org/10.1039/c2gc36534kopenalex-snapshot
Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: nitrile hydrations and beyond
inferredcites →https://doi.org/10.1039/c2ob26930aopenalex-snapshot
Direct amide formation using radiofrequency heating
inferredcites →https://doi.org/10.1039/c2ra22459copenalex-snapshot
Hypervalent iodine catalyzed transamidation of carboxamides with amines
inferredcites →https://doi.org/10.1039/c3gc40225hopenalex-snapshot
Development of GSK's reagent guides – embedding sustainability into reagent selection
inferredcites →https://doi.org/10.1039/c3ob27367aopenalex-snapshot
Mechanism of arylboronic acid-catalyzed amidation reaction between carboxylic acids and amines
inferredcites →https://doi.org/10.1039/jr9650005142openalex-snapshot
954. Trisdialkylaminoboranes: new reagents for the synthesis of enamines and amides
inferredcites →https://doi.org/10.1055/s-0028-1083277openalex-snapshot
The Thermal Amidation of Carboxylic Acids Revisited
inferredcites →https://doi.org/10.1055/s-0032-1316993openalex-snapshot
Titanium(IV) Isopropoxide as an Efficient Catalyst for Direct Amidation of Nonactivated Carboxylic Acids
inferredcites →https://doi.org/10.1055/s-1975-23900openalex-snapshot
A Convenient Method of Amidation of Carboxylic Acids Using Boron Trifluoride Etherate
inferredcites →https://doi.org/10.1055/s-2001-16788openalex-snapshot
3,5-Bis(perfluorodecyl)phenylboronic Acid as an Easily Recyclable Direct Amide Condensation Catalyst
inferredcites →https://doi.org/10.1080/00397910500297180openalex-snapshot
Transamidation Catalyzed by a Recoverable and Reusable PolyDMAP‐Based Hafnium Chloride and Montmorillonite KSF
inferredcites →https://doi.org/10.1080/00397919308013807openalex-snapshot
A Simple Preparation of Amides from Acids and Amines by Heating of Their Mixture
inferredcites →https://doi.org/10.15227/orgsyn.081.0262openalex-snapshot
BORIC ACID CATALYZED AMIDE FORMATION FROM CARBOXYLIC ACIDS AND AMINES: N-BENZYL-4-PHENYLBUTYRAMIDE
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/047084289x.rn01754openalex-snapshot
Tris(2,2,2-trifluoroethoxy)boron
inferred← citeshttps://doi.org/10.1002/0471264229.os092.22openalex-snapshot
Dipeptide Syntheses via Activated α‐Aminoesters
inferred← citeshttps://doi.org/10.1002/9783527693931.ch1openalex-snapshot
Different Roles of Carboxylic Functions in Pharmaceuticals and Agrochemicals
inferred← citeshttps://doi.org/10.1002/9783527830190.ch14openalex-snapshot
Natural Phosphates and Their Catalytic Applications
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/admi.201500022openalex-snapshot
Selective Absorption of Hydrophobic Cations in Nanostructured Porous Materials from Crosslinked Hydrogen‐Bonded Columnar Liquid Crystals
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.201400648openalex-snapshot
Synthesis of Secondary Amides from N‐Substituted Amidines by Tandem Oxidative Rearrangement and Isocyanate Elimination
inferred← citeshttps://doi.org/10.1002/adsc.201700034openalex-snapshot
Sequential One‐Pot Synthesis of Dipeptides through the Transient Formation of CDI‐N‐Protected α‐Aminoesters
inferred← citeshttps://doi.org/10.1002/adsc.201700619openalex-snapshot
A Visible‐Light‐Driven, Metal‐free Route to Aromatic Amides via Radical Arylation of Isonitriles
inferred← citeshttps://doi.org/10.1002/adsc.201801061openalex-snapshot
Biocatalytic N‐Acylation of Amines in Water Using an Acyltransferase from Mycobacterium smegmatis
inferred← citeshttps://doi.org/10.1002/adsc.201801096openalex-snapshot
Copper‐Catalyzed Site‐Selective Oxidative C−C Bond Cleavage of Simple Ketones for the Synthesis of Anilides and Paracetamol
inferred← citeshttps://doi.org/10.1002/adsc.202200607openalex-snapshot
An Umpolung Route to Amides from α‐Aminonitriles under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/adsc.202300376openalex-snapshot
Palladium and Copper‐Catalyzed Friedel–Crafts Acylation with Activated Amides
inferred← citeshttps://doi.org/10.1002/adsc.202300487openalex-snapshot
Synthesis of Bulky N‐Acyl Heterocycles by DMAPO/Boc2O‐Mediated One‐Pot Direct N‐Acylation of Less Nucleophilic N‐Heterocycles with α‐Fully Substituted Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/adsc.202401441openalex-snapshot
N‐Heterocyclic Carbene‐Diboron‐Substrate Cooperatively Facilitate Direct Amidation of Carboxylic Acids and Amines
inferred← citeshttps://doi.org/10.1002/ajoc.201600590openalex-snapshot
Montmorillonite‐K10‐Catalyzed Microwave‐Assisted Direct Amidation of Unactivated Carboxylic Acids with Amines: Maintaining Chiral Integrity of Substrates
inferred← citeshttps://doi.org/10.1002/ajoc.201800070openalex-snapshot
Heterobimetallic Lanthanide–Sodium Alkoxides Catalyze the Amidation of Esters
inferred← citeshttps://doi.org/10.1002/ajoc.201800258openalex-snapshot
Cerium Catalyzed Transamidation of Secondary Amides under Ultrasound Irradiation: A Breakthrough in Organic Synthesis
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.202000237openalex-snapshot
Transition‐Metal‐Free, Visible‐Light‐Mediated N‐acylation: An Efficient Route to Amides in Water
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.202200315openalex-snapshot
Synthesis of Glycouronamides by Transamidation Approach at Room Temperature
inferred← citeshttps://doi.org/10.1002/ajoc.202200454openalex-snapshot
Copper‐catalyzed C(sp3)−H/N−H Cross Dehydrogenative Coupling Between Toluene Derivatives and Picolinamides
inferred← citeshttps://doi.org/10.1002/ajoc.202300660openalex-snapshot
Dehydrative Condensation of Carboxylic Acids with Amines Promoted by HBF4/MS 5A
inferred← citeshttps://doi.org/10.1002/ajoc.202400528openalex-snapshot
Recent Advances in Direct Amidation Via Organocatalysis
inferred← citeshttps://doi.org/10.1002/ajoc.70171openalex-snapshot
Experimental and Theoretical Mechanistic Study on the 6‐Iodo‐2‐pyridone‐Catalyzed Aminolysis of Esters
inferred← citeshttps://doi.org/10.1002/ange.201402147openalex-snapshot
Inverse Peptide Synthesis via Activated α‐Aminoesters
inferred← citeshttps://doi.org/10.1002/ange.201605162openalex-snapshot
Nickel‐Catalyzed Reductive Amidation of Unactivated Alkyl Bromides
inferred← citeshttps://doi.org/10.1002/ange.201606120openalex-snapshot
9‐Silafluorenyl Dichlorides as Chemically Ligating Coupling Agents and Their Application in Peptide Synthesis
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.202000224openalex-snapshot
Amide Synthesis by Nickel/Photoredox‐Catalyzed Direct Carbamoylation of (Hetero)Aryl Bromides
inferred← citeshttps://doi.org/10.1002/ange.202011339openalex-snapshot
Regio‐ and Enantioselective Ni‐Catalyzed Formal Hydroalkylation, Hydrobenzylation, and Hydropropargylation of Acrylamides to α‐Tertiary Amides
inferred← citeshttps://doi.org/10.1002/ange.202106412openalex-snapshot
Direct Amidation of Esters by Ball Milling**
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/ange.202207472openalex-snapshot
Photo‐Excited Nickel‐Catalyzed Silyl‐Radical‐Mediated Direct Activation of Carbamoyl Chlorides To Access (Hetero)aryl Carbamides**
inferred← citeshttps://doi.org/10.1002/ange.202303264openalex-snapshot
Translating Planar Heterocycles into Three‐Dimensional Analogs by Photoinduced Hydrocarboxylation**
inferred← citeshttps://doi.org/10.1002/ange.202405152openalex-snapshot
Effiziente enzymatische Synthese von Carbamaten in Wasser durch promiskuitive Esterasen/Acyltransferasen
inferred← citeshttps://doi.org/10.1002/anie.201402147openalex-snapshot
Inverse Peptide Synthesis via Activated α‐Aminoesters
inferred← citeshttps://doi.org/10.1002/anie.201605162openalex-snapshot
Nickel‐Catalyzed Reductive Amidation of Unactivated Alkyl Bromides
inferred← citeshttps://doi.org/10.1002/anie.201606120openalex-snapshot
9‐Silafluorenyl Dichlorides as Chemically Ligating Coupling Agents and Their Application in Peptide Synthesis
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.202000224openalex-snapshot
Amide Synthesis by Nickel/Photoredox‐Catalyzed Direct Carbamoylation of (Hetero)Aryl Bromides
inferred← citeshttps://doi.org/10.1002/anie.202011339openalex-snapshot
Regio‐ and Enantioselective Ni‐Catalyzed Formal Hydroalkylation, Hydrobenzylation, and Hydropropargylation of Acrylamides to α‐Tertiary Amides
inferred← citeshttps://doi.org/10.1002/anie.202106412openalex-snapshot
Direct Amidation of Esters by Ball Milling**
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/anie.202207472openalex-snapshot
Photo‐Excited Nickel‐Catalyzed Silyl‐Radical‐Mediated Direct Activation of Carbamoyl Chlorides To Access (Hetero)aryl Carbamides**
inferred← citeshttps://doi.org/10.1002/anie.202303264openalex-snapshot
Translating Planar Heterocycles into Three‐Dimensional Analogs by Photoinduced Hydrocarboxylation**
inferred← citeshttps://doi.org/10.1002/anie.202405152openalex-snapshot
Efficient Enzymatic Synthesis of Carbamates in Water Using Promiscuous Esterases/Acyltransferases
inferred← citeshttps://doi.org/10.1002/aoc.5517openalex-snapshot
Facile amidation of esters with aromatic amines promoted by lanthanide tris (amide) complexes
inferred← citeshttps://doi.org/10.1002/aoc.5911openalex-snapshot
Promising new catalytic properties of a Co (II)‐carboxamide complex and its derived Co3O4 nanoparticles for the Mizoroki‐Heck and the Epoxidation reactions
inferred← citeshttps://doi.org/10.1002/aoc.6808openalex-snapshot
[NN]‐Chelate nickel complexes with Schiff base ligands: Synthesis, structure and catalytic activity in green amidation reaction
inferred← citeshttps://doi.org/10.1002/aoc.7228openalex-snapshot
N‐alkylation of benzamides/sulfonamides using alcohols via borrowing hydrogen approach by well‐defined Pd (II) pincer complexes
inferred← citeshttps://doi.org/10.1002/app.45985openalex-snapshot
Preparation and characterizations of RTV epoxy blends using amide maleic anhydride‐g‐liquid polybutadience as both reactive toughening and curing components
inferred← citeshttps://doi.org/10.1002/asia.201601111openalex-snapshot
Regioselective Functionalization of 3‐Hydroxy‐pyridine Carboxylates by Neighboring Group Assistance
inferred← citeshttps://doi.org/10.1002/asia.201601421openalex-snapshot
Synthesis of Amides and Phthalimides via a Palladium Catalyzed Aminocarbonylation of Aryl Halides with Formic Acid and Carbodiimides
inferred← citeshttps://doi.org/10.1002/asia.202300738openalex-snapshot
Dual Role of TiO(acac)2 as a Reagent and an Activator/Catalyst: A Study on the Solvent Dependent Product Formation
inferred← citeshttps://doi.org/10.1002/asia.70979openalex-snapshot
Direct Mechano‐Catalytic Synthesis of Amides Using Brass Balls via Cross‐Coupling of Isocyanides With Arylboronic Acids or in Situ Generated N‐Aryl‐Pyridinium Salts
inferred← citeshttps://doi.org/10.1002/cctc.201500601openalex-snapshot
A Heterogeneous Niobium(V) Oxide Catalyst for the Direct Amidation of Esters
inferred← citeshttps://doi.org/10.1002/cctc.201500672openalex-snapshot
Amidation of Carboxylic Acids with Amines by Nb2O5 as a Reusable Lewis Acid Catalyst
inferred← citeshttps://doi.org/10.1002/cctc.202000881openalex-snapshot
Iron‐catalyzed hydrosilylation of diacids in the presence of amines: a new route to cyclic amines
inferred← citeshttps://doi.org/10.1002/cctc.202201596openalex-snapshot
DMAPO/Boc2O‐Mediated One‐Pot Direct N‐Acylation of Less Nucleophilic N‐Heterocycles with Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/cctc.202500359openalex-snapshot
Oxidative N‐Formylation of Amines to Formamides
inferred← citeshttps://doi.org/10.1002/chem.201402029openalex-snapshot
Efficient Palladium‐Catalyzed Aminocarbonylation of Aryl Iodides Using Palladium Nanoparticles Dispersed on Siliceous Mesocellular Foam
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/chem.201800372openalex-snapshot
Protecting‐Group‐Free Amidation of Amino Acids using Lewis Acid Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201804077openalex-snapshot
Synthesis of Aliphatic Carboxamides Mediated by Nickel NN2‐Pincer Complexes and Adaptation to Carbon‐Isotope Labeling
inferred← citeshttps://doi.org/10.1002/chem.201900715openalex-snapshot
All Non‐Carbon B3NO2 Exotic Heterocycles: Synthesis, Dynamics, and Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201904717openalex-snapshot
A Hydroperoxide‐Mediated Decarboxylation of α‐Ketoacids Enables the Chemoselective Acylation of Amines
inferred← citeshttps://doi.org/10.1002/chem.202102300openalex-snapshot
Supported CuII Single‐Ion Catalyst for Total Carbon Utilization of C2 and C3 Biomass‐Based Platform Molecules in the N‐Formylation of Amines
inferred← citeshttps://doi.org/10.1002/chem.202302023openalex-snapshot
Ruthenium‐Catalyzed Aminocarbonylation with Isocyanates Through Weak Coordinating Groups
inferred← citeshttps://doi.org/10.1002/chem.202404345openalex-snapshot
A Cytotoxic Indazole‐based Gold(III) Carboxamide Pincer Complex Targeting DNA Through Dual Binding Modes of Groove Binding and Alkylation
inferred← citeshttps://doi.org/10.1002/chem.202500595openalex-snapshot
Skeletal Rearrangements of Amides via Breaking Inert Bonds
inferred← citeshttps://doi.org/10.1002/chem.202500862openalex-snapshot
Ru‐Catalyzed Deoxygenative Functionalization of Phenols via π‐Coordination Activation: Mechanochemical Access to N‐Aryl Amides and α‐Aryl Carbonyls
inferred← citeshttps://doi.org/10.1002/chin.201406249openalex-snapshot
ChemInform Abstract: Recent Developments in Amide Synthesis: Direct Amidation of Carboxylic Acids and Transamidation Reactions
inferred← citeshttps://doi.org/10.1002/cjoc.201400253openalex-snapshot
Water‐Promoted Ring‐Opening Reactions of N‐Substituted Saccharins and Phthalimides by Amines
inferred← citeshttps://doi.org/10.1002/cjoc.201900252openalex-snapshot
Ketone Synthesis by Direct, Orthogonal Chemoselective Hydroacylation of Alkenes with Amides: Use of Alkenes as Surrogates of Alkyl Carbanions
inferred← citeshttps://doi.org/10.1002/cjoc.202300396openalex-snapshot
Iron‐Catalyzed Amide Bond Formation from Carboxylic Acids and Isocyanates†
inferred← citeshttps://doi.org/10.1002/cnma.201500123openalex-snapshot
Self‐Heating Approach to the Fast Production of Uniform Metal Nanostructures
inferred← citeshttps://doi.org/10.1002/cssc.201403469openalex-snapshot
Efficient Synthesis of Amides and Esters from Alcohols under Aerobic Ambient Conditions Catalyzed by a Au/Mesoporous Al 2 O 3 Nanocatalyst
inferred← citeshttps://doi.org/10.1002/cssc.201500526openalex-snapshot
Pharmaceuticals and Surfactants from Alga‐Derived Feedstock: Amidation of Fatty Acids and Their Derivatives with Amino Alcohols
inferred← citeshttps://doi.org/10.1002/cssc.202102708openalex-snapshot
Amide Bonds Meet Flow Chemistry: A Journey into Methodologies and Sustainable Evolution
inferred← citeshttps://doi.org/10.1002/ejlt.201600483openalex-snapshot
Effect of water and lipophilic alcohols or amines on the 4‐dodecylbenzenesulfonic acid‐catalyzed esterifications, trans‐esterifications, and amidations
inferred← citeshttps://doi.org/10.1002/ejoc.201403173openalex-snapshot
Iron/Caffeine as a Catalytic System for Microwave‐Promoted Benzamide Formation
inferred← citeshttps://doi.org/10.1002/ejoc.201501349openalex-snapshot
Nickel‐Catalyzed Reductive Addition of Aryl/Benzyl Halides and Pseudohalides to Carbodiimides for the Synthesis of Amides
inferred← citeshttps://doi.org/10.1002/ejoc.201600186openalex-snapshot
Bio‐Based Amides from Renewable Isosorbide by a Direct and Atom‐Economic Boric Acid Amidation Methodology
inferred← citeshttps://doi.org/10.1002/ejoc.201601276openalex-snapshot
Mechanochemical Synthesis of Dipeptides Using Mg‐Al Hydrotalcite as Activating Agent under Solvent‐Free Reaction Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201700961openalex-snapshot
Mechanochemistry for Organic Chemists: An Update
inferred← citeshttps://doi.org/10.1002/ejoc.201701802openalex-snapshot
Synthesis of Secondary Amides through the Palladium(II)‐Catalyzed Aminocarbonylation of Arylboronic Acids with Amines or Hydrazines and Carbon Monoxide
inferred← citeshttps://doi.org/10.1002/ejoc.201800175openalex-snapshot
Forging Amides Through Metal‐Catalyzed C–C Coupling with Isocyanates
inferred← citeshttps://doi.org/10.1002/ejoc.201800378openalex-snapshot
Synthesis of Amides from Alcohols and Amines Through a Domino Oxidative Amidation and Telescoped Transamidation Process
inferred← citeshttps://doi.org/10.1002/ejoc.201801567openalex-snapshot
Unexpected Reactivity of N‐Acyl‐Benzotriazoles with Aromatic Amines in Acidic Medium (ABAA Reaction)
inferred← citeshttps://doi.org/10.1002/ejoc.201901291openalex-snapshot
Solvent‐Free N‐Alkylation of Amides with Alcohols Catalyzed by Nickel on Silica–Alumina
inferred← citeshttps://doi.org/10.1002/ejoc.201901495openalex-snapshot
Lewis Base Catalysis Promoted Nucleophilic Substitutions – Recent Advances and Future Directions
inferred← citeshttps://doi.org/10.1002/ejoc.202000080openalex-snapshot
Amide Bond Formation Strategies: Latest Advances on a Dateless Transformation
inferred← citeshttps://doi.org/10.1002/ejoc.202301010openalex-snapshot
Cross‐Linked Pseudopeptides via Pd‐Catalyzed Carbonylative Coupling of α‐Amino Acid Iodides with α‐Amino Acid Esters in the Presence of a CO Surrogate
inferred← citeshttps://doi.org/10.1002/ejoc.202400315openalex-snapshot
Copper‐Promoted Oxidative Amidation of Imines: A Facile Route to Amides
inferred← citeshttps://doi.org/10.1002/ejoc.202401229openalex-snapshot
Metal‐Free Direct Synthesis of Secondary Amides and Nitriles Using O‐(2‐Pyrimidinyl)‐N‐Boc Hydroxylamine
inferred← citeshttps://doi.org/10.1002/ejoc.202500210openalex-snapshot
Recent Advances in Transition Metal‐Free Strategies for the Transformation of Amides into Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/hc.21364openalex-snapshot
A high‐efficient method for the amidation of carboxylic acids promoted by triphenylphosphine oxide and oxalyl chloride
inferred← citeshttps://doi.org/10.1002/jhet.4786openalex-snapshot
Chemoselective direct amidation of fatty acids with furfurylamine without coupling reagents in reversed micellar microenvironment
inferred← citeshttps://doi.org/10.1002/kin.21334openalex-snapshot
A high yield method for the direct amidation of long‐chain fatty acids
inferred← citeshttps://doi.org/10.1002/slct.201601965openalex-snapshot
Solvent‐, and Catalyst–free Acylation of Anilines with Meldrum's Acids: ANeat Access to Anilides
inferred← citeshttps://doi.org/10.1002/slct.201800048openalex-snapshot
Efficient Catalyst‐Free Trans Sulfonamidation/Sulfonamide Metathesis under Mild Conditions
inferred← citeshttps://doi.org/10.1002/slct.201903444openalex-snapshot
Efficient and Chemoselective Amidation of β ‐Carboline Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/slct.201904254openalex-snapshot
Ultrasound Promoted Oxamate Synthesis: A Chemoselective and Direct Approach from Amines
inferred← citeshttps://doi.org/10.1002/slct.202100808openalex-snapshot
Sunlight Photocatalytic Synthesis of Aryl Hydrazides by Decatungstate‐Promoted Acylation under Room Temperature
inferred← citeshttps://doi.org/10.1002/slct.202200861openalex-snapshot
Efficient Synthesis of 4‐Bromo‐ N ‐(1‐phenylethyl)benzamide, Arylation by Pd(0) Catalyst, Characterization and DFT Study
inferred← citeshttps://doi.org/10.1002/slct.202506605openalex-snapshot
Bis(phenolate)–Titanium(IV) Catalysts for Efficient and Sustainable Direct Amide Bond Formation
inferred← citeshttps://doi.org/10.1002/slct.202507148openalex-snapshot
Sodium Borohydride‐Promoted, Pd/AlO(OH)‐Catalyzed Green Oxidation of Aryl Aldehydes to Benzoic Acids in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/slct.74404openalex-snapshot
Emerging Trends in Using Thiuram Disulfides as Promising Amine and Thiocarbamoyl Sources for Facile Amidation and Thioamidation Reactions
inferred← citeshttps://doi.org/10.1002/slct.74569openalex-snapshot
Copper(II) Acetate as a Dual‐Function Reagent: A Useful Acetyl Source for the In Situ N‐Acetylation of Anilines
inferred← citeshttps://doi.org/10.1002/sus2.193openalex-snapshot
Electrocatalytic synthesis of C–N coupling compounds from CO 2 and nitrogenous species
inferred← citeshttps://doi.org/10.1002/tcr.201800132openalex-snapshot
Practical and Scalable Organic Reactions with Flow Microwave Apparatus
inferred← citeshttps://doi.org/10.1002/tcr.201900072openalex-snapshot
Transition‐Metal‐Free Activation of Amides by N−C Bond Cleavage
inferred← citeshttps://doi.org/10.1002/tcr.202100224openalex-snapshot
Direct Access to Amides from Nitro‐Compounds via Aminocarbonylation and Amidation Reactions: A Minireview
inferred← citeshttps://doi.org/10.1002/tcr.202300020openalex-snapshot
Recent Advances in Carbon‐Nitrogen/Carbon‐Oxygen Bond Formation Under Transition‐Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/tcr.202500029openalex-snapshot
Transition Metal‐Catalyzed Aminocarbonylation Reactions
inferred← citeshttps://doi.org/10.1002/wnan.70070openalex-snapshot
Engineering Functional Graphenic Materials for Bone Repair
inferred← citeshttps://doi.org/10.1007/s11030-021-10252-0openalex-snapshot
Catalytic and non-catalytic amidation of carboxylic acid substrates
inferred← citeshttps://doi.org/10.1007/s11084-019-09575-8openalex-snapshot
Prebiotic Syntheses Under Shock in the Water – Formamide – Potassium Bicarbonate – Sodium Hydroxide System
inferred← citeshttps://doi.org/10.1007/s11172-022-3473-7openalex-snapshot
Tandem silylation—desilylation reaction in the synthesis of N-methyl carboxamides
inferred← citeshttps://doi.org/10.1007/s11426-024-2539-xopenalex-snapshot
Recent progress in electrocatalytic C-N coupling of CO2 and inorganic N-containing small molecules
inferred← citeshttps://doi.org/10.1007/s11696-021-01636-5openalex-snapshot
CAL-B-mediated efficient synthesis of a set of valuable amides by direct amidation of phenoxy- and aryl-propionic acids
inferred← citeshttps://doi.org/10.1007/s12274-024-6732-0openalex-snapshot
Overcoming side reaction effects in the colloidal synthesis of ZnSe/ZnS core/shell quantum dots with an etching strategy
inferred← citeshttps://doi.org/10.1007/s40201-019-00440-4openalex-snapshot
Adsorptive removal of oil spill from sea water surface using magnetic wood sawdust as a novel nano-composite synthesized via microwave approach
inferred← citeshttps://doi.org/10.1016/b978-0-12-819848-3.00002-5openalex-snapshot
Microwave-assisted C N formation reactions
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/b978-0-323-96025-0.00100-9openalex-snapshot
Going Green: Sustainable Alternatives in Organic Synthesis
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.2024.120084openalex-snapshot
Metal-free decarboxylative oxygenation of α-amino acids to amide compounds via photoredox catalysis
inferred← citeshttps://doi.org/10.1016/j.apcato.2024.206998openalex-snapshot
Environmentally benign aminolysis of lactones in acidic hydrophobic ionic liquids
inferred← citeshttps://doi.org/10.1016/j.apenergy.2024.124808openalex-snapshot
Insights into the effect of various supports on hydrothermal liquefaction of food waste over iron-oxide nano-catalysts
inferred← citeshttps://doi.org/10.1016/j.apsusc.2018.09.039openalex-snapshot
Design of thermally stable insulation film by radical grafting poly(methylacrylic acid) on silicon surface
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109529openalex-snapshot
Design, catalyst-free synthesis, DFT study and anticancer assessment of new 2,9-disubstituted purine-6-carboxamides
inferred← citeshttps://doi.org/10.1016/j.bios.2017.02.028openalex-snapshot
Synthesis of novel monomeric graphene quantum dots and corresponding nanocomposite with molecularly imprinted polymer for electrochemical detection of an anticancerous ifosfamide drug
inferred← citeshttps://doi.org/10.1016/j.catcom.2014.05.007openalex-snapshot
Self-catalyzed direct amidation of ketones: A sustainable procedure for acetaminophen synthesis
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.09.007openalex-snapshot
Copper-catalyzed amide bond formation from formamides and carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.cej.2025.163493openalex-snapshot
Efficient and stable heterogeneous Pd-catalyzed regioselective Anti-Markovnikov carbonylative coupling of alkenes with amines
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2019.124276openalex-snapshot
Polyelectrolyte coated individual silica nanoparticles dispersed in concentrated divalent brine at elevated temperatures for subsurface energy applications
inferred← citeshttps://doi.org/10.1016/j.cplett.2026.142922openalex-snapshot
Carbon dots with food-compatible molecules for surface functionalization: synthesis, properties, and antimicrobial activities
inferred← citeshttps://doi.org/10.1016/j.esci.2022.11.002openalex-snapshot
Recent progress in electrochemical C–N coupling reactions
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.04.008openalex-snapshot
Carbonylative transformation of aryl halides and strong bonds via cheap metal catalysts and sustainable technologies
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.ijbiomac.2026.151582openalex-snapshot
Reprogramming regioselectivity of nitrile hydratase towards adiponitrile via semi-rational design of a key “switch” residue
inferred← citeshttps://doi.org/10.1016/j.jece.2017.12.059openalex-snapshot
Citric acid-silane modified zirconia nanoparticles: Preparation, characterization and adsorbent efficiency
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121555openalex-snapshot
New half-sandwich (η6-p-cymene)ruthenium(II) complexes with benzothiazole hydrazone Schiff base ligand: Synthesis, structural characterization and catalysis in transamidation of carboxamide with primary amines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123290openalex-snapshot
Recent developments in metal-catalysed transamidation of quiescent amides
inferred← citeshttps://doi.org/10.1016/j.mencom.2019.11.029openalex-snapshot
Amide derivatives of 3-aminopropylsilatrane
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.molstruc.2020.129076openalex-snapshot
Preparation and catalytic evaluation of a palladium catalyst deposited over modified clinoptilolite (Pd@MCP) for chemoselective N-formylation and N-acylation of amines
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131512openalex-snapshot
Synthesis, biological activity, structure activity relationship study and liposomal formulation development of some arylsulfonyl pyroglutamic acid derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142575openalex-snapshot
Integrated synthesis, characterization, and computational analysis of 1H pyrrole-1,2,4-oxadiazole hybrids as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142971openalex-snapshot
Synthesis, DFT, Molecular docking and Photophysical studies of novel benzimidazole appended pyrrolidine derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146020openalex-snapshot
Antimetastatic activity evaluation of diamides inspired by SRPK inhibitor N-[2-(piperidin-1-yl)-5-(trifluoromethyl) phenyl] isonicotinamide (SRPIN340)
inferred← citeshttps://doi.org/10.1016/j.poly.2022.115906openalex-snapshot
Synthesis, chemical and physical properties of lanthanide(III) (Nd, Gd, Tb) complexes derived from (E)-ethyl 4-(2-hydroxybenzylideneamino)benzoate
inferred← citeshttps://doi.org/10.1016/j.polymer.2026.130261openalex-snapshot
Herbal dihydrocoumarin as latent monophenol to bisamide-bridged bisphenols for fully biobased epoxy resins
inferred← citeshttps://doi.org/10.1016/j.progpolymsci.2018.03.002openalex-snapshot
Polymer engineering based on reversible covalent chemistry: A promising innovative pathway towards new materials and new functionalities
inferred← citeshttps://doi.org/10.1016/j.rechem.2021.100253openalex-snapshot
Novel versatile synthesis method for amides, carbamates and ureas employing a Grignard base, an amine and an ester
inferred← citeshttps://doi.org/10.1016/j.rser.2026.117038openalex-snapshot
Advances in anodic electrocatalysts enabling coupled organonitrogen electrosynthesis and hydrogen production
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.2015.04.074openalex-snapshot
A general method for the direct transformation of common tertiary amides into ketones and amines by addition of Grignard reagents
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.2018.10.030openalex-snapshot
Triphenyl borate catalyzed synthesis of amides from carboxylic acids and amines
inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.027openalex-snapshot
N-triflyl-propiolamides: Preparation and transamidation reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133066openalex-snapshot
Copper-catalyzed benzylic C–H amidation of toluene derivatives with N-(8-quinolyl)amides through C(sp3)–H/N–H cross dehydrogenative coupling
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133291openalex-snapshot
A comprehensive solvent-free approach for the esterification and amidation of carboxylic acids mediated by carbodiimides
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.11.015openalex-snapshot
Synthesis of β-hydroxyacetamides from unactivated ethyl acetates under base-free conditions and microwave irradiation
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.2014.10.124openalex-snapshot
Scandium triflate catalyzed ester synthesis using primary amides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.02.090openalex-snapshot
Facile synthesis and biological evaluation of assorted indolyl-3-amides and esters from a single, stable carbonyl nitrile intermediate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.05.118openalex-snapshot
Microwave-promoted direct amidation of unactivated esters catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.050openalex-snapshot
Carboxyl activation via silylthioesterification: one-pot, two-step amidation of carboxylic acids catalyzed by non-metal ammonium salts
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.2018.01.097openalex-snapshot
Conquering amide planarity: Structural distortion and its hidden reactivity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.05.003openalex-snapshot
Highly efficient synthesis of aryl ketones by PEPPSI-palladium catalyzed acylative Suzuki coupling of amides with diarylborinic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.05.065openalex-snapshot
Recent advances in chemoselective acylation of amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.11.036openalex-snapshot
Repurposing n-butyl stannoic acid as highly efficient catalyst for direct amidation of carboxylic acids with amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.04.040openalex-snapshot
NH4I-promoted N-acylation of amines via the transamidation of DMF and DMA under metal-free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152399openalex-snapshot
An unprecedented cobalt-catalyzed selective aroylation of primary amines with aroyl peroxides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152605openalex-snapshot
Nickel-catalyzed aminocarbonylation of Aryl/Alkenyl/Allyl (pseudo)halides with isocyanides and H2O
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153990openalex-snapshot
N-ethyltetramethylguanidinium ionic liquid [ETMG][EtSO3] as organocatalyst and solvent for facile amide synthesis by formyl-transfer with N-formyl-saccharin
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154718openalex-snapshot
One-pot silyl imidate formation-N-alkylation reactions of amides with propargyl propionates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155813openalex-snapshot
Phosphine-mediated deoxygenative synthesis of amides from carboxylic acids and N-chloro compounds
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00443openalex-snapshot
Recent Developments in General Methodologies for the Synthesis of α-Ketoamides
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00237openalex-snapshot
Nonclassical Routes for Amide Bond Formation
inferred← citeshttps://doi.org/10.1021/acs.iecr.5b03279openalex-snapshot
Low Adsorption of Magnetite Nanoparticles with Uniform Polyelectrolyte Coatings in Concentrated Brine on Model Silica and Sandstone
inferred← citeshttps://doi.org/10.1021/acs.iecr.8b00498openalex-snapshot
Unprecedented Ester–Amide Exchange Reaction Using Highly Versatile Two-Dimensional Graphene Oxide Supported Base Metal Nanocatalyst
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c00886openalex-snapshot
Intermetallic Pd–Sn Nanoparticles on Supports with High Metal Loading Facilitated by the Metal–Metal Bond for High-Performance Cooperative Catalysis
inferred← citeshttps://doi.org/10.1021/acs.jced.8b00887openalex-snapshot
Functional Ionic Liquid-Capped Graphene Quantum Dots for Chromium Removal from Chromium Contaminated Water
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00188openalex-snapshot
Radical-Mediated Activation of Esters with a Copper/Selectfluor System: Synthesis of Bulky Amides and Peptides
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01792openalex-snapshot
Regioselective Synthesis of 2° Amides Using Visible-Light-Induced Photoredox-Catalyzed Nonaqueous Oxidative C–N Cleavage of N,N-Dibenzylanilines
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02245openalex-snapshot
Transamidation and Decarbonylation of N-Phthaloyl-Amino Acid Amides Enabled by Palladium-Catalyzed Selective C–N Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01288openalex-snapshot
Amine Activation: “Inverse” Dipeptide Synthesis and Amide Function Formation through Activated Amino Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02394openalex-snapshot
Visible Light-Mediated Carbamoylation of para-Quinone Methides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00585openalex-snapshot
On the Use of Triarylsilanols as Catalysts for Direct Amidation of Carboxylic Acids
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
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