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Amide activation: an emerging tool for chemoselective synthesis

https://doi.org/10.1039/c8cs00335a
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inferredcites →https://doi.org/10.1002/(sici)1521-3773(19990917)38:18<2728::aid-anie2728>3.0.co;2-0openalex-snapshot
A Convergent Strategy for the Asymmetric Synthesis of Enantiomerically Pure Bicyclic Compounds by Using a Silicon-Directed Cycloaddition Reaction: The Synthesis of Enantiomerically Pure Bicyclo[3.2.0]hept-2-en-6-one
inferredcites →https://doi.org/10.1002/0471264229.os089.53openalex-snapshot
Direct Synthesis of Azaheterocycles from N ‐Aryl/Vinyl Amides. Synthesis of 4‐(Methylthio)‐2‐phenylquinazoline and 4‐(4‐Methoxyphenyl)‐2‐phenylquinoline
inferredcites →https://doi.org/10.1002/adsc.201600373openalex-snapshot
An Efficient Heterobimetallic Lanthanide Alkoxide Catalyst for Transamidation of Amides under Solvent‐Free Conditions
inferredcites →https://doi.org/10.1002/ajoc.201200066openalex-snapshot
Versatile and Direct Transformation of Secondary Amides into Ketones by Deaminative Alkylation with Organocerium Reagents
inferredcites →https://doi.org/10.1002/anie.196904541openalex-snapshot
Alkyl and Aryl α‐Chloro Enamines
inferredcites →https://doi.org/10.1002/anie.197208522openalex-snapshot
α‐Chloroenamines: New Reagents for Organic Synthesis
inferredcites →https://doi.org/10.1002/anie.197402671openalex-snapshot
A Convenient Procedure for the Synthesis of Cyclobutanones
inferredcites →https://doi.org/10.1002/anie.197402672openalex-snapshot
A General Method for the Synthesis of 2‐Azetidinones and 2‐Azetidinylideneammonium Salts
inferredcites →https://doi.org/10.1002/anie.197505691openalex-snapshot
Cyclobutenylideneammonium Salts from the Cycloadditions of Keteniminium Salts to Acetylenes
inferredcites →https://doi.org/10.1002/anie.198107821openalex-snapshot
[2 + 2]‐Cycloaddition of N,N‐Dimethyl‐N(2‐methyl‐1‐propenylidene)ammonium (“Tetramethylketeniminium”) Ion to α,β‐Unsaturated Carbonyl Compounds
inferredcites →https://doi.org/10.1002/anie.198108791openalex-snapshot
Cyclobutanone and Cyclobutenone Derivatives by Reaction of Tertiary Amides with Alkenes or Alkynes
inferredcites →https://doi.org/10.1002/anie.200906416openalex-snapshot
Unexpected Electrophilic Rearrangements of Amides: A Stereoselective Entry to Challenging Substituted Lactones
inferredcites →https://doi.org/10.1002/anie.201000652openalex-snapshot
Direct, One‐pot Sequential Reductive Alkylation of Lactams/Amides with Grignard and Organolithium Reagents through Lactam/Amide Activation
inferredcites →https://doi.org/10.1002/anie.201007100openalex-snapshot
Farewell to the HSAB Treatment of Ambident Reactivity
inferredcites →https://doi.org/10.1002/anie.201200387openalex-snapshot
A Concise and Versatile Double‐Cyclization Strategy for the Highly Stereoselective Synthesis and Arylative Dimerization of Aspidosperma Alkaloids
inferredcites →https://doi.org/10.1002/anie.201204098openalex-snapshot
Direct Transformation of Secondary Amides into Secondary Amines: Triflic Anhydride Activated Reductive Alkylation
inferredcites →https://doi.org/10.1002/anie.201402229openalex-snapshot
Chemoselective Intermolecular α‐Arylation of Amides
inferredcites →https://doi.org/10.1002/anie.201405609openalex-snapshot
Concise and Enantioselective Total Synthesis of (−)‐Mehranine, (−)‐Methylenebismehranine, and Related Aspidosperma Alkaloids
inferredcites →https://doi.org/10.1002/anie.201507776openalex-snapshot
General Olefin Synthesis by the Palladium‐Catalyzed Heck Reaction of Amides: Sterically Controlled Chemoselective NC Activation
inferredcites →https://doi.org/10.1002/anie.201511385openalex-snapshot
Synthesis of Highly Functionalized 4‐Aminoquinolines
inferredcites →https://doi.org/10.1002/anie.201601914openalex-snapshot
Synthesis of Biaryls through Nickel‐Catalyzed Suzuki–Miyaura Coupling of Amides by Carbon–Nitrogen Bond Cleavage
inferredcites →https://doi.org/10.1002/anie.201603068openalex-snapshot
Nickel‐Catalyzed Decarbonylative Borylation of Amides: Evidence for Acyl C−N Bond Activation
inferredcites →https://doi.org/10.1002/anie.201607856openalex-snapshot
Nickel‐Catalyzed Esterification of Aliphatic Amides
inferredcites →https://doi.org/10.1002/anie.201611819openalex-snapshot
Catalytic Ester and Amide to Amine Interconversion: Nickel‐Catalyzed Decarbonylative Amination of Esters and Amides by C−O and C−C Bond Activation
inferredcites →https://doi.org/10.1002/anie.201612624openalex-snapshot
Selective Reductive Removal of Ester and Amide Groups from Arenes and Heteroarenes through Nickel‐Catalyzed C−O and C−N Bond Activation
inferredcites →https://doi.org/10.1002/anie.201701538openalex-snapshot
Metal‐Free Formal Oxidative C−C Coupling by In Situ Generation of an Enolonium Species
inferredcites →https://doi.org/10.1002/anie.201703174openalex-snapshot
Mizoroki–Heck Cyclizations of Amide Derivatives for the Introduction of Quaternary Centers
inferredcites →https://doi.org/10.1002/anie.201703667openalex-snapshot
Hydroxamic Acids as Chemoselective (ortho‐Amino)arylation Reagents via Sigmatropic Rearrangement
inferredcites →https://doi.org/10.1002/anie.201707102openalex-snapshot
Decarbonylative Phosphorylation of Amides by Palladium and Nickel Catalysis: The Hirao Cross‐Coupling of Amide Derivatives
inferredcites →https://doi.org/10.1002/anie.201708088openalex-snapshot
Enantioselective Total Synthesis of (−)‐Deoxoapodine
inferredcites →https://doi.org/10.1002/anie.201708665openalex-snapshot
Nucleophilic Arylation of N , O ‐Ketene Acetals with Triaryl Aluminum Reagents: Access to α‐Aryl Amides through an Umpolung Process
inferredcites →https://doi.org/10.1002/asia.201100108openalex-snapshot
Revisiting Keteniminium Salts: More than the Nitrogen Analogs of Ketenes
inferredcites →https://doi.org/10.1002/cber.19290620221openalex-snapshot
Imid‐ und Amidchloride nicht‐aromatischer Säuren (III. Mitteilung)
inferredcites →https://doi.org/10.1002/chem.201002054openalex-snapshot
Versatile One‐Pot Reductive Alkylation of Lactams/Amides via Amide Activation: Application to the Concise Syntheses of Bioactive Alkaloids (±)‐Bgugaine, (±)‐Coniine, (+)‐Preussin, and (−)‐Cassine
inferredcites →https://doi.org/10.1002/chem.201003591openalex-snapshot
Steering Reaction Pathways: From Benzyl Claisen Rearrangements to Powerful Ionic Shifts
inferredcites →https://doi.org/10.1002/chem.201203293openalex-snapshot
Dual Nucleophilic/Electrophilic Capture of In Situ Generated Iminium Ethers: Towards the Synthesis of Functionalized Amide Building Blocks
inferredcites →https://doi.org/10.1002/chem.201203906openalex-snapshot
Direct Room‐Temperature Lactonisation of Alcohols and Ethers onto Amides: An “Amide Strategy” for Synthesis
inferredcites →https://doi.org/10.1002/chem.201302096openalex-snapshot
General One‐Pot Reductive gem‐Bis‐Alkylation of Tertiary Lactams/Amides: Rapid Construction of 1‐Azaspirocycles and Formal Total Synthesis of (±)‐Cephalotaxine
inferredcites →https://doi.org/10.1002/chem.201602484openalex-snapshot
Nucleophilic and Electrophilic Activation of Non‐Heteroaromatic Amides in Atom‐Economical Asymmetric Catalysis
inferredcites →https://doi.org/10.1002/chem.201602717openalex-snapshot
Highly Chemoselective Synthesis of Indolizidine Lactams by SmI2‐Induced Umpolung of the Amide Bond via Aminoketyl Radicals: Efficient Entry to Alkaloid Scaffolds
inferredcites →https://doi.org/10.1002/chem.201605012openalex-snapshot
Twisted Amides: From Obscurity to Broadly Useful Transition‐Metal‐Catalyzed Reactions by N−C Amide Bond Activation
inferredcites →https://doi.org/10.1002/chem.201702608openalex-snapshot
Cobalt‐Catalyzed Esterification of Amides
inferredcites →https://doi.org/10.1002/chem.201703239openalex-snapshot
Catalytic Asymmetric Total Synthesis and Stereochemical Revision of Leucinostatin A: A Modulator of Tumor–Stroma Interaction
inferredcites →https://doi.org/10.1002/chem.201703832openalex-snapshot
Synthesis of Functionalized Quinolines through a Reaction of Amides and Alkynes Promoted by Triflic Anhydride/Pyridine
inferredcites →https://doi.org/10.1002/chem.201705842openalex-snapshot
Nickel‐Catalyzed C−S Bond Formation via Decarbonylative Thioetherification of Esters, Amides and Intramolecular Recombination Fragment Coupling of Thioesters
inferredcites →https://doi.org/10.1002/cmdc.201700568openalex-snapshot
C2‐Modified Sparteine Derivatives Are a New Class of Potentially Long‐Acting Sodium Channel Blockers
inferredcites →https://doi.org/10.1002/hlca.19710540229openalex-snapshot
Sulfidkontraktion via alkylative Kupplung: Eine methode zur darstellung von β‐dicarbonylderivaten. Über synthetische methoden, 1. Mitteilung
inferredcites →https://doi.org/10.1002/hlca.19770600108openalex-snapshot
A New Total Synthesis of dl‐Pumiliotoxin‐C via an Indanone
inferredcites →https://doi.org/10.1002/jlac.18771840102openalex-snapshot
Ueber die Einwirkung von Phosphorpentachlorid auf Säureamide
inferredcites →https://doi.org/10.1016/0040-4039(80)88066-xopenalex-snapshot
A convenient method for the selective reduction of amides to amines
inferredcites →https://doi.org/10.1016/j.bmcl.2014.03.044openalex-snapshot
Synthesis of strigolactones analogues by intramolecular [2+2] cycloaddition of ketene-iminium salts to olefins and their activity on Orobanche cumana seeds
inferredcites →https://doi.org/10.1016/j.saa.2013.09.108openalex-snapshot
Synthesis, spectral, and anti-microbial studies of thioiminium iodides and amine hydrochlorides
inferredcites →https://doi.org/10.1016/j.tet.2012.01.085openalex-snapshot
A concise and divergent approach to radicamine B and hyacinthacine A3 based on a step-economic transformation
inferredcites →https://doi.org/10.1016/j.tet.2015.06.027openalex-snapshot
Investigation of cationic Claisen-type electrophilic rearrangements of amides
inferredcites →https://doi.org/10.1016/j.tetlet.2011.09.016openalex-snapshot
Total synthesis of (−)-nakadomarin A: alkyne ring-closing metathesis
inferredcites →https://doi.org/10.1016/j.tetlet.2012.06.013openalex-snapshot
A novel approach toward the synthesis of strigolactones through intramolecular [2+2] cycloaddition of ketenes and ketene-iminiums to olefins. Application to the asymmetric synthesis of GR-24
inferredcites →https://doi.org/10.1016/j.tetlet.2014.10.040openalex-snapshot
Asymmetric synthesis of the four stereoisomers of 5-deoxystrigol
inferredcites →https://doi.org/10.1016/j.tetlet.2015.09.103openalex-snapshot
Access to functionalized 3-amino-benzothiophenes using keteniminium intermediates
inferredcites →https://doi.org/10.1016/s0040-4020(00)00093-4openalex-snapshot
Chemical Transformations Induced by Triflic Anhydride
inferredcites →https://doi.org/10.1016/s0040-4020(02)00243-0openalex-snapshot
Synthesis of the Kopsia alkaloids (±)-pauciflorine B, (±)-lahadinine B, (±)-kopsidasine, (±)-kopsidasine-N-oxide, (±)-kopsijasminilam and (±)-11-methoxykopsilongine
inferredcites →https://doi.org/10.1016/s0040-4020(03)00920-7openalex-snapshot
A short multigram asymmetric synthesis of prostanoid scaffolds
inferredcites →https://doi.org/10.1016/s0040-4039(00)79386-5openalex-snapshot
An efficient method for the vicinal acylation of unactivated olefins using keteniminium salts derived from protected α-Hydroxy- or α-Aminoacids.
inferredcites →https://doi.org/10.1016/s0040-4039(00)81896-1openalex-snapshot
Nonstereospecificity in the cycloadditions of keteneiminium salts to olefins. Evidence for a stepwise mechanism.
inferredcites →https://doi.org/10.1016/s0040-4039(00)85171-0openalex-snapshot
Intramolecular cycloadditions of keteniminium salts. A novel approach toward prostaglandins
inferredcites →https://doi.org/10.1016/s0040-4039(00)92145-2openalex-snapshot
The enantioselective fluoroacetamide acetal claisen rearrangements of N-fluoroacetyl-trans-(2R,5R)-2,5-dimethylpyrrolidine
inferredcites →https://doi.org/10.1016/s0040-4039(00)97650-0openalex-snapshot
Study of chiral auxiliaries for the intramolecular [2+2] cycloaddition of a keteniminium salt to an olefinic double bond. A new asymmetric synthesis of cyclobutanones.
inferredcites →https://doi.org/10.1016/s0040-4039(01)91114-1openalex-snapshot
Vicinal alkylation of alkynes. A short route toward Δα,β butenolides, furans and cyclopentenones.
inferredcites →https://doi.org/10.1016/s0040-4039(01)91316-4openalex-snapshot
N-methoxy-n-methylamides as effective acylating agents
inferredcites →https://doi.org/10.1016/s0040-4039(01)98583-1openalex-snapshot
Synthesis and reactions of 2-amino-1-azirines
inferredcites →https://doi.org/10.1016/s0040-4039(97)10310-0openalex-snapshot
A new method for the conversion of secondary and tertiary amides to bridged orthoesters
inferredcites →https://doi.org/10.1016/s0040-4039(98)02228-xopenalex-snapshot
1,3-Asymmetric induction in the intramolecular [2+2] cycloaddition of alkene-keteniminium salts. Synthesis of (+)-gibberellic acid key intermediate
inferredcites →https://doi.org/10.1016/s0957-4166(00)80017-8openalex-snapshot
Intramolecular cycloadditions of keteniminium salts. A practical asymmetric synthesis of prostaglandins.
inferredcites →https://doi.org/10.1016/s0957-4166(98)00249-3openalex-snapshot
Enantioselective synthesis of the trans-2,6-dialkylpiperidine alkaloids (2R,6R)-lupetidine and (2R,6R)-solenopsin A
inferredcites →https://doi.org/10.1021/acs.joc.5b00881openalex-snapshot
Determination of Structures and Energetics of Small- and Medium-Sized One-Carbon-Bridged Twisted Amides using ab Initio Molecular Orbital Methods: Implications for Amidic Resonance along the C–N Rotational Pathway
inferredcites →https://doi.org/10.1021/acs.joc.5b01023openalex-snapshot
Direct Observation of Intermediates Involved in the Interruption of the Bischler–Napieralski Reaction
inferredcites →https://doi.org/10.1021/acs.joc.6b00572openalex-snapshot
Mild Metal-Free Hydrosilylation of Secondary Amides to Amines
inferredcites →https://doi.org/10.1021/acs.joc.6b00675openalex-snapshot
Making the Least Reactive Electrophile the First in Class: Domino Electrophilic Activation of Amides
inferredcites →https://doi.org/10.1021/acs.joc.6b01835openalex-snapshot
Studies toward Total Synthesis of (±)-Caldaphnidine C via One-Pot Sequential Intramolecular Vilsmeier–Haack and Azomethine Ylide 1,3-Dipolar Cycloaddition
inferredcites →https://doi.org/10.1021/acs.joc.6b02294openalex-snapshot
N -Acylsaccharins as Amide-Based Arylating Reagents via Chemoselective N–C Cleavage: Pd-Catalyzed Decarbonylative Heck Reaction
inferredcites →https://doi.org/10.1021/acs.joc.7b00971openalex-snapshot
Resonance Destabilization in N-Acylanilines (Anilides): Electronically-Activated Planar Amides of Relevance in N–C(O) Cross-Coupling
inferredcites →https://doi.org/10.1021/acs.joc.7b02150openalex-snapshot
Reductive Alkylation of Tertiary Lactams via Addition of Organocopper (RCu) Reagents to Thioiminium Ions
inferredcites →https://doi.org/10.1021/acs.joc.7b02868openalex-snapshot
Chemoselective Reduction of Sterically Demanding N , N -Diisopropylamides to Aldehydes
inferredcites →https://doi.org/10.1021/acs.orglett.5b00128openalex-snapshot
One-Pot Synthesis of 3,4,5-Trisubstituted 1,2,4-Triazoles via the Addition of Hydrazides to Activated Secondary Amides
inferredcites →https://doi.org/10.1021/acs.orglett.5b00765openalex-snapshot
Rapid Access to 3-Aminoindazoles from Tertiary Amides
inferredcites →https://doi.org/10.1021/acs.orglett.5b02209openalex-snapshot
Sterically Controlled Pd-Catalyzed Chemoselective Ketone Synthesis via N–C Cleavage in Twisted Amides
inferredcites →https://doi.org/10.1021/acs.orglett.6b00058openalex-snapshot
Rhodium-Catalyzed C–H Bond Functionalization with Amides by Double C–H/C–N Bond Activation
inferredcites →https://doi.org/10.1021/acs.orglett.6b00842openalex-snapshot
Chemoselective Ketone Synthesis by the Addition of Organometallics to N-Acylazetidines
inferredcites →https://doi.org/10.1021/acs.orglett.6b01836openalex-snapshot
N -Acylsaccharins: Stable Electrophilic Amide-Based Acyl Transfer Reagents in Pd-Catalyzed Suzuki–Miyaura Coupling via N–C Cleavage
inferredcites →https://doi.org/10.1021/acs.orglett.6b02952openalex-snapshot
Nickel-Catalyzed Diaryl Ketone Synthesis by N–C Cleavage: Direct Negishi Cross-Coupling of Primary Amides by Site-Selective N,N-Di-Boc Activation
inferredcites →https://doi.org/10.1021/acs.orglett.6b03550openalex-snapshot
Asymmetric Total Synthesis of Lepadiformine C Using Memory of Chirality in an Intramolecular Ester Enolate Michael Addition
inferredcites →https://doi.org/10.1021/acs.orglett.7b00373openalex-snapshot
Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling of N-Mesylamides by N–C Cleavage: Electronic Effect of the Mesyl Group
inferredcites →https://doi.org/10.1021/acs.orglett.7b00429openalex-snapshot
Metal-Free Transamidation of Secondary Amides via Selective N–C Cleavage under Mild Conditions
inferredcites →https://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
inferredcites →https://doi.org/10.1021/acs.orglett.7b00831openalex-snapshot
Ni-Catalyzed Reductive Cross-Coupling of Amides with Aryl Iodide Electrophiles via C–N Bond Activation
inferredcites →https://doi.org/10.1021/acs.orglett.7b01004openalex-snapshot
Direct Regioselective Synthesis of Tetrazolium Salts by Activation of Secondary Amides under Mild Conditions
inferredcites →https://doi.org/10.1021/acs.orglett.7b01194openalex-snapshot
Amide to Alkyne Interconversion via a Nickel/Copper-Catalyzed Deamidative Cross-Coupling of Aryl and Alkenyl Amides
inferredcites →https://doi.org/10.1021/acs.orglett.7b01199openalex-snapshot
Decarbonylative Cyanation of Amides by Palladium Catalysis
inferredcites →https://doi.org/10.1021/acs.orglett.7b01575openalex-snapshot
Suzuki–Miyaura Cross-Coupling of N-Acylpyrroles and Pyrazoles: Planar, Electronically Activated Amides in Catalytic N–C Cleavage
inferredcites →https://doi.org/10.1021/acs.orglett.7b02877openalex-snapshot
Palladium(II)/N-Heterocyclic Carbene-Catalyzed Direct C–H Acylation of Heteroarenes with N-Acylsaccharins
inferredcites →https://doi.org/10.1021/acs.orglett.7b03943openalex-snapshot
Enamines as Surrogates of Alkene Carbanions for the Reductive Alkenylation of Secondary Amides: An Approach to Allylamines
inferredcites →https://doi.org/10.1021/acs.orglett.8b00949openalex-snapshot
Palladium-Catalyzed Decarbonylative Alkynylation of Amides
inferredcites →https://doi.org/10.1021/acscatal.6b00793openalex-snapshot
Nickel-Catalyzed Alkylation of Amide Derivatives
inferredcites →https://doi.org/10.1021/acscatal.6b02323openalex-snapshot
Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling of Amides via Site-Selective N–C Bond Cleavage by Cooperative Catalysis
inferredcites →https://doi.org/10.1021/acscatal.6b03040openalex-snapshot
Nickel-Catalyzed Deamidative Step-Down Reduction of Amides to Aromatic Hydrocarbons
inferredcites →https://doi.org/10.1021/acscatal.6b03277openalex-snapshot
Breaking Amides using Nickel Catalysis
inferredcites →https://doi.org/10.1021/acscatal.6b03616openalex-snapshot
General Method for the Suzuki–Miyaura Cross-Coupling of Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (NHC =N-Heterocyclic Carbene) Complexes
inferredcites →https://doi.org/10.1021/acscatal.7b02540openalex-snapshot
Site-Selective C–H/C–N Activation by Cooperative Catalysis: Primary Amides as Arylating Reagents in Directed C–H Arylation
inferredcites →https://doi.org/10.1021/acscatal.7b02599openalex-snapshot
Zn-Catalyzed tert -Butyl Nicotinate-Directed Amide Cleavage as a Biomimic of Metallo-Exopeptidase Activity
inferredcites →https://doi.org/10.1021/acscatal.7b02859openalex-snapshot
Nickel-Catalyzed Reductive Transamidation of Secondary Amides with Nitroarenes
inferredcites →https://doi.org/10.1021/acscatal.7b03688openalex-snapshot
Nickel-Catalyzed Suzuki–Miyaura Coupling of Aliphatic Amides
inferredcites →https://doi.org/10.1021/cr00087a005openalex-snapshot
Intramolecular cycloaddition reactions of ketenes and keteniminium salts with alkenes
inferredcites →https://doi.org/10.1021/ja00173a029openalex-snapshot
Relationship between amidic distortion and ease of hydrolysis in base. If amidic resonance does not exist, then what accounts for the accelerated hydrolysis of distorted amides?
inferredcites →https://doi.org/10.1021/ja00189a036openalex-snapshot
Synthesis and absolute configuration of the Aristotelia alkaloid peduncularine
inferredcites →https://doi.org/10.1021/ja00293a073openalex-snapshot
Intramolecular [2+2] cycloadditions of ketenes and keteniminium salts to olefins
inferredcites →https://doi.org/10.1021/ja00374a036openalex-snapshot
Models for asymmetric [2+2] cycloadditions
inferredcites →https://doi.org/10.1021/ja00509a060openalex-snapshot
.alpha.,.beta. Dehydrogenation of carboxamides
inferredcites →https://doi.org/10.1021/ja00763a062openalex-snapshot
Cycloadditions of keteneimmonium cations to olefins and dienes. New synthesis of four-membered rings
inferredcites →https://doi.org/10.1021/ja01048a059openalex-snapshot
Direct alkyl and aryl amination of heteroaromatic nitrogen compounds
inferredcites →https://doi.org/10.1021/ja017136xopenalex-snapshot
Practical and Highly Regio- and Stereoselective Synthesis of 2-Substituted Dihydropyridines and Piperidines: Application to the Synthesis of (−)-Coniine
inferredcites →https://doi.org/10.1021/ja050420uopenalex-snapshot
Can Decarbonylation of Acyl Radicals Be Overcome in Radical Addition Reactions? En Route to a Solution Employing N-Acyl Oxazolidinones and SmI2/H2O
inferredcites →https://doi.org/10.1021/ja060626aopenalex-snapshot
Synthesis of Substituted Pyridine Derivatives via the Ruthenium-Catalyzed Cycloisomerization of 3-Azadienynes
inferredcites →https://doi.org/10.1021/ja066405mopenalex-snapshot
Single-Step Synthesis of Pyrimidine Derivatives
inferredcites →https://doi.org/10.1021/ja073912aopenalex-snapshot
Direct Synthesis of Pyridine Derivatives
inferredcites →https://doi.org/10.1021/ja077463qopenalex-snapshot
Highly Chemoselective Metal-Free Reduction of Tertiary Amides
inferredcites →https://doi.org/10.1021/ja105194sopenalex-snapshot
Controlled and Chemoselective Reduction of Secondary Amides
inferredcites →https://doi.org/10.1021/ja404673sopenalex-snapshot
Total Synthesis of (−)-Nakadomarin A
inferredcites →https://doi.org/10.1021/ja408856popenalex-snapshot
Electrophilic Rearrangements of Chiral Amides: A Traceless Asymmetric α-Allylation
inferredcites →https://doi.org/10.1021/ja412578topenalex-snapshot
Highly Chemoselective Reduction of Amides (Primary, Secondary, Tertiary) to Alcohols using SmI 2 /Amine/H 2 O under Mild Conditions
inferredcites →https://doi.org/10.1021/ja805706ropenalex-snapshot
Synthesis of Indoles via Domino Reaction of N -Aryl Amides and Ethyl Diazoacetate
inferredcites →https://doi.org/10.1021/jacs.6b04061openalex-snapshot
Chemo- and Stereoselective Transition-Metal-Free Amination of Amides with Azides
inferredcites →https://doi.org/10.1021/jacs.6b04086openalex-snapshot
Radical–Radical Cyclization Cascades of Barbiturates Triggered by Electron-Transfer Reduction of Amide-Type Carbonyls
inferredcites →https://doi.org/10.1021/jacs.6b07623openalex-snapshot
Concise Total Syntheses of (+)-Haplocidine and (+)-Haplocine via Late-Stage Oxidation of (+)-Fendleridine Derivatives
inferredcites →https://doi.org/10.1021/jacs.6b12077openalex-snapshot
Dearomatizing Radical Cyclizations and Cyclization Cascades Triggered by Electron-Transfer Reduction of Amide-Type Carbonyls
inferredcites →https://doi.org/10.1021/jacs.7b02983openalex-snapshot
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inferredcites →https://doi.org/10.1021/jacs.7b06191openalex-snapshot
Ni-Catalyzed Alkene Carboacylation via Amide C–N Bond Activation
inferredcites →https://doi.org/10.1021/jacs.7b08813openalex-snapshot
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inferredcites →https://doi.org/10.1021/jacs.7b09482openalex-snapshot
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inferredcites →https://doi.org/10.1021/jacs.7b11309openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo00035a007openalex-snapshot
Daphniphyllum alkaloids. 10. Classical total synthesis of methyl homodaphniphyllate
inferredcites →https://doi.org/10.1021/jo00225a038openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo00381a019openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo00387a020openalex-snapshot
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inferredcites →https://doi.org/10.1021/jo010461iopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jo025927ropenalex-snapshot
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inferredcites →https://doi.org/10.1021/jo0266083openalex-snapshot
Enantioselective Synthesis of Piperidine, Indolizidine, and Quinolizidine Alkaloids from a Phenylglycinol-Derived δ-Lactam
inferredcites →https://doi.org/10.1021/jo0344485openalex-snapshot
Mild Method for the Conversion of Amides to Thioamides
inferredcites →https://doi.org/10.1021/jo052141vopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jo202042xopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jo302362bopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jo4007656openalex-snapshot
A Direct and General Method for the Reductive Alkylation of Tertiary Lactams/Amides: Application to the Step Economical Synthesis of Alkaloid (−)-Morusimic Acid D
inferredcites →https://doi.org/10.1021/jo502522xopenalex-snapshot
SmI 2 -Mediated Radical Coupling Strategy to Securinega Alkaloids: Total Synthesis of (−)-14,15-Dihydrosecurinine and Formal Total Synthesis of (−)-Securinine
inferredcites →https://doi.org/10.1021/jo502929xopenalex-snapshot
A General Method for the One-Pot Reductive Functionalization of Secondary Amides
inferredcites →https://doi.org/10.1021/jo802355dopenalex-snapshot
Direct Dehydrative N-Pyridinylation of Amides
inferredcites →https://doi.org/10.1021/jo971883oopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol0516519openalex-snapshot
Addition of Tethered Nonaromatic Carbon Nucleophiles to Chemoselectively Activated Amides
inferredcites →https://doi.org/10.1021/ol052069nopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol202629dopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol302165dopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol401465yopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol503432bopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol801264uopenalex-snapshot
A Versatile Cyclodehydration Reaction for the Synthesis of Isoquinoline and β-Carboline Derivatives
inferredcites →https://doi.org/10.1021/ol802010nopenalex-snapshot
A Versatile Cascade of Intramolecular Vilsmeier−Haack and Azomethine Ylide 1,3-Dipolar Cycloaddition toward Tricyclic Cores of Alkaloids
inferredcites →https://doi.org/10.1021/ol902767bopenalex-snapshot
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inferredcites →https://doi.org/10.1021/op2003826openalex-snapshot
Large-Scale Carbonyl Reductions in the Pharmaceutical Industry
inferredcites →https://doi.org/10.1038/nature14615openalex-snapshot
Conversion of amides to esters by the nickel-catalysed activation of amide C–N bonds
inferredcites →https://doi.org/10.1038/nchem.1268openalex-snapshot
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inferredcites →https://doi.org/10.1038/nchem.2388openalex-snapshot
Nickel-catalysed Suzuki–Miyaura coupling of amides
inferredcites →https://doi.org/10.1038/ncomms11554openalex-snapshot
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inferredcites →https://doi.org/10.1038/ncomms14993openalex-snapshot
Nickel-catalysed retro-hydroamidocarbonylation of aliphatic amides to olefins
inferredcites →https://doi.org/10.1039/c39730000165openalex-snapshot
Intermediacy of a keten in the “homo-Favorskii” reaction
inferredcites →https://doi.org/10.1039/c39800000173openalex-snapshot
2-Amino-1-azetines, a new class of strained amidines
inferredcites →https://doi.org/10.1039/c3cc43665aopenalex-snapshot
Versatile construction of functionalized tropane ring systems based on lactam activation: enantioselective synthesis of (+)-pervilleine B
inferredcites →https://doi.org/10.1039/c3qo00065fopenalex-snapshot
A versatile two-step method for the reductive alkylation and formal [4 + 2] annulation of secondary lactams: step economical syntheses of the ant venom alkaloids (2R,5S)-2-butyl-5-propylpyrrolidine and (+)-monomorine I
inferredcites →https://doi.org/10.1039/c4cc03826fopenalex-snapshot
Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones
inferredcites →https://doi.org/10.1039/c5cc00430fopenalex-snapshot
Acylative Suzuki coupling of amides: acyl-nitrogen activation via synergy of independently modifiable activating groups
inferredcites →https://doi.org/10.1039/c6cc06428kopenalex-snapshot
Palladium-catalyzed Sonogashira coupling of amides: access to ynones via C–N bond cleavage
inferredcites →https://doi.org/10.1039/c7cs00182gopenalex-snapshot
Cross-coupling of aromatic esters and amides
inferredcites →https://doi.org/10.1039/c7ob00739fopenalex-snapshot
Selective construction of quaternary stereocentres in radical cyclisation cascades triggered by electron-transfer reduction of amide-type carbonyls
inferredcites →https://doi.org/10.1039/c7sc01980gopenalex-snapshot
Nickel-catalyzed transamidation of aliphatic amide derivatives
inferredcites →https://doi.org/10.1055/s-0036-1588458openalex-snapshot
Recent Advances in Cyclic Diacyl Peroxides: Reactivity and Selectivity Enhancement Brought by the Cyclic Structure
inferredcites →https://doi.org/10.1055/s-0036-1588845openalex-snapshot
Nickel-Catalyzed Negishi Cross-Coupling of N-Acylsuccinimides: Stable, Amide-Based, Twist-Controlled Acyl-Transfer Reagents via N–C Activation
inferredcites →https://doi.org/10.1055/s-1993-25934openalex-snapshot
The Conversion of Secondary Amides to Tetrazoles with Trifluoromethanesulfonic Anhydride and Sodium Azide
inferredcites →https://doi.org/10.1246/cl.1995.53openalex-snapshot
1,2-Asymmetric Induction in the Intramolecular [2+2] Cycloadditions of Keteniminium Salts. Enantioselective Syntheses of (−)-Dihydroactinidiolide and (−)-Anastrephin
inferredcites →https://doi.org/10.15227/orgsyn.089.0549openalex-snapshot
Direct Synthesis of Azaheterocycles from N-Aryl/Vinyl Amides. Synthesis of 4-(Methylthio)-2-phenylquinazoline and 4-(4-Methoxyphenyl)-2-phenylquinoline

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/0471264229.os099.20openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527830251.ch4openalex-snapshot
Transition‐Metal‐Free Reactions of Amides by Tetrahedral Intermediates
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inferred← citeshttps://doi.org/10.1002/adsc.201801577openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.202000122openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.202200607openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.202300218openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.202301018openalex-snapshot
Contemporary Approaches for Amide Bond Formation
inferred← citeshttps://doi.org/10.1002/adsc.202400008openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.202400402openalex-snapshot
Cu‐Catalyzed Reaction of Trifluoromethylated β‐Keto Diazos and Nitriles Proceeding via H2O Addition to Nitrile Ylides
inferred← citeshttps://doi.org/10.1002/adsc.70249openalex-snapshot
Recent Advances in the Activation of Unactivated Tertiary Amide C–N Bonds
inferred← citeshttps://doi.org/10.1002/advs.202513012openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.202300473openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.202400528openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.70261openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201900233openalex-snapshot
Controlled Reduction of Carboxamides to Alcohols or Amines by Zinc Hydrides
inferred← citeshttps://doi.org/10.1002/ange.201901049openalex-snapshot
Approach to Fully Substituted Cyclic Nitrones from N‐Hydroxylactam Derivatives: Development and Application to the Total Synthesis of Cylindricine C
inferred← citeshttps://doi.org/10.1002/ange.202004272openalex-snapshot
Transition‐Metal‐Free Reductive Functionalization of Tertiary Carboxamides and Lactams for α‐Branched Amine Synthesis
inferred← citeshttps://doi.org/10.1002/ange.202012048openalex-snapshot
Reductive Arylation of Amides via a Nickel‐Catalyzed Suzuki–Miyaura‐Coupling and Transfer‐Hydrogenation Cascade
inferred← citeshttps://doi.org/10.1002/ange.202015898openalex-snapshot
Enantioselective Reductive Cyanation and Phosphonylation of Secondary Amides by Iridium and Chiral Thiourea Sequential Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202101775openalex-snapshot
Three‐Component Aminoarylation of Electron‐Rich Alkenes by Merging Photoredox with Nickel Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202102518openalex-snapshot
Unified Synthesis of Polycyclic Alkaloids by Complementary Carbonyl Activation**
inferred← citeshttps://doi.org/10.1002/ange.202104023openalex-snapshot
Chemoselektive γ‐Oxidation von β,γ‐ungesättigten Amiden mit TEMPO
inferred← citeshttps://doi.org/10.1002/ange.202104359openalex-snapshot
Merging Electron Transfer with 1,2‐Metalate Rearrangement: Deoxygenative Arylation of Aromatic Amides with Arylboronic Esters
inferred← citeshttps://doi.org/10.1002/ange.202106716openalex-snapshot
Expedient Synthesis of Bridged Bicyclic Nitrogen Scaffolds via Orthogonal Tandem Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202111029openalex-snapshot
Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202114146openalex-snapshot
Mechanochemical Solvent‐Free Suzuki–Miyaura Cross‐Coupling of Amides via Highly Chemoselective N−C Cleavage
inferred← citeshttps://doi.org/10.1002/ange.202115497openalex-snapshot
Deoxygenative Cross‐Coupling of Aromatic Amides with Polyfluoroarenes
inferred← citeshttps://doi.org/10.1002/ange.202201574openalex-snapshot
Ni‐Catalyzed Divergent Synthesis of 2‐Benzazepine Derivatives via Tunable Cyclization and 1,4‐Acyl Transfer Triggered by Amide N‐C Bond Cleavage
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.202206170openalex-snapshot
Selective Reduction of Secondary Amides to Imines Catalysed by Schwartz's Reagent**
inferred← citeshttps://doi.org/10.1002/ange.202208978openalex-snapshot
α‐Thianthrenium Carbonyl Species: The Equivalent of an α‐Carbonyl Carbocation
inferred← citeshttps://doi.org/10.1002/ange.202212213openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202215008openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202302832openalex-snapshot
Concise Total Synthesis of (−)‐Quinocarcin Enabled by Catalytic Enantioselective Reductive 1,3‐Dipolar Cycloaddition of Secondary Amides
inferred← citeshttps://doi.org/10.1002/ange.202304990openalex-snapshot
Transfer freier Aminogruppen via α‐Aminierung von Carbonylen
inferred← citeshttps://doi.org/10.1002/ange.202309567openalex-snapshot
Reactivity Umpolung of Tertiary Amide Enabled by Catalytic Reductive Stannylation
inferred← citeshttps://doi.org/10.1002/ange.202316579openalex-snapshot
Sulfonium Rearrangements Enable the Direct Preparation of Sulfenyl Imidinium Salts
inferred← citeshttps://doi.org/10.1002/ange.202317290openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202411990openalex-snapshot
Deoxygenative Geminal Silylboration of Amides Using Silylboronates: Synthesis and Use of α‐Boryl‐α‐Silylalkylamines
inferred← citeshttps://doi.org/10.1002/ange.202412152openalex-snapshot
Photoredox‐Catalyzed [3+2] annulation of Aromatic Amides with Olefins via Iminium Intermediates
inferred← citeshttps://doi.org/10.1002/ange.202418070openalex-snapshot
Asymmetrische Synthese von β‐Ketoamiden durch eine Sulfoniumumlagerung
inferred← citeshttps://doi.org/10.1002/ange.202422742openalex-snapshot
Catalytic Reductive Amination and Tandem Amination–Alkylation of Esters Enabled by a Cationic Iridium Complex
inferred← citeshttps://doi.org/10.1002/ange.202425305openalex-snapshot
Isoselenourea‐Catalyzed Enantioselective Pyrazolo‐Heterocycle Synthesis Enabled by Self‐Correcting Amide and Ester Acylation
inferred← citeshttps://doi.org/10.1002/ange.202500170openalex-snapshot
Asymmetric Synthesis of S(IV)‐Stereogenic Sulfinimidate Esters by Sulfinamide Activation
inferred← citeshttps://doi.org/10.1002/ange.202508062openalex-snapshot
Total Synthesis of Isodaphlongamine H by Iridium‐Catalyzed Reductive [3 + 2] Cycloaddition of N‐ Hydroxylactam
inferred← citeshttps://doi.org/10.1002/ange.202513359openalex-snapshot
Steering Amide Synthesis from Acetonitrile by Electrochemically Derived Active Superoxide
inferred← citeshttps://doi.org/10.1002/ange.4999077openalex-snapshot
Catalytic Selective Deoxygenation and Deamination of Amides to Access Alkenes
inferred← citeshttps://doi.org/10.1002/ange.8873247openalex-snapshot
Electroreductive Radical C–C Acylation Coupling from N , N ‐Dimethylamides and Organic Halides via Inert C(O)−N Bond Cleavage: Facile Access to Aryl Ketones
inferred← citeshttps://doi.org/10.1002/anie.201900233openalex-snapshot
Controlled Reduction of Carboxamides to Alcohols or Amines by Zinc Hydrides
inferred← citeshttps://doi.org/10.1002/anie.201901049openalex-snapshot
Approach to Fully Substituted Cyclic Nitrones from N‐Hydroxylactam Derivatives: Development and Application to the Total Synthesis of Cylindricine C
inferred← citeshttps://doi.org/10.1002/anie.202004272openalex-snapshot
Transition‐Metal‐Free Reductive Functionalization of Tertiary Carboxamides and Lactams for α‐Branched Amine Synthesis
inferred← citeshttps://doi.org/10.1002/anie.202012048openalex-snapshot
Reductive Arylation of Amides via a Nickel‐Catalyzed Suzuki–Miyaura‐Coupling and Transfer‐Hydrogenation Cascade
inferred← citeshttps://doi.org/10.1002/anie.202015898openalex-snapshot
Enantioselective Reductive Cyanation and Phosphonylation of Secondary Amides by Iridium and Chiral Thiourea Sequential Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202101775openalex-snapshot
Three‐Component Aminoarylation of Electron‐Rich Alkenes by Merging Photoredox with Nickel Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202102518openalex-snapshot
Unified Synthesis of Polycyclic Alkaloids by Complementary Carbonyl Activation**
inferred← citeshttps://doi.org/10.1002/anie.202104023openalex-snapshot
Chemoselective γ‐Oxidation of β,γ‐Unsaturated Amides with TEMPO
inferred← citeshttps://doi.org/10.1002/anie.202104359openalex-snapshot
Merging Electron Transfer with 1,2‐Metalate Rearrangement: Deoxygenative Arylation of Aromatic Amides with Arylboronic Esters
inferred← citeshttps://doi.org/10.1002/anie.202106716openalex-snapshot
Expedient Synthesis of Bridged Bicyclic Nitrogen Scaffolds via Orthogonal Tandem Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202111029openalex-snapshot
Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202114146openalex-snapshot
Mechanochemical Solvent‐Free Suzuki–Miyaura Cross‐Coupling of Amides via Highly Chemoselective N−C Cleavage
inferred← citeshttps://doi.org/10.1002/anie.202115497openalex-snapshot
Deoxygenative Cross‐Coupling of Aromatic Amides with Polyfluoroarenes
inferred← citeshttps://doi.org/10.1002/anie.202201574openalex-snapshot
Ni‐Catalyzed Divergent Synthesis of 2‐Benzazepine Derivatives via Tunable Cyclization and 1,4‐Acyl Transfer Triggered by Amide N‐C Bond Cleavage
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.202206170openalex-snapshot
Selective Reduction of Secondary Amides to Imines Catalysed by Schwartz's Reagent**
inferred← citeshttps://doi.org/10.1002/anie.202208978openalex-snapshot
α‐Thianthrenium Carbonyl Species: The Equivalent of an α‐Carbonyl Carbocation
inferred← citeshttps://doi.org/10.1002/anie.202212213openalex-snapshot
Challenges and Breakthroughs in Selective Amide Activation
inferred← citeshttps://doi.org/10.1002/anie.202215008openalex-snapshot
Recent Applications of Trifluoromethanesulfonic Anhydride in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.202302832openalex-snapshot
Concise Total Synthesis of (−)‐Quinocarcin Enabled by Catalytic Enantioselective Reductive 1,3‐Dipolar Cycloaddition of Secondary Amides
inferred← citeshttps://doi.org/10.1002/anie.202304990openalex-snapshot
Free Amino Group Transfer via α‐Amination of Native Carbonyls
inferred← citeshttps://doi.org/10.1002/anie.202309567openalex-snapshot
Reactivity Umpolung of Tertiary Amide Enabled by Catalytic Reductive Stannylation
inferred← citeshttps://doi.org/10.1002/anie.202316579openalex-snapshot
Sulfonium Rearrangements Enable the Direct Preparation of Sulfenyl Imidinium Salts
inferred← citeshttps://doi.org/10.1002/anie.202317290openalex-snapshot
Iridium‐Catalyzed Reductive (3+2) Annulation of Lactams Enabling the Rapid Total Synthesis of (±)‐Eburnamonine
inferred← citeshttps://doi.org/10.1002/anie.202411990openalex-snapshot
Deoxygenative Geminal Silylboration of Amides Using Silylboronates: Synthesis and Use of α‐Boryl‐α‐Silylalkylamines
inferred← citeshttps://doi.org/10.1002/anie.202412152openalex-snapshot
Photoredox‐Catalyzed [3+2] annulation of Aromatic Amides with Olefins via Iminium Intermediates
inferred← citeshttps://doi.org/10.1002/anie.202418070openalex-snapshot
Asymmetric Synthesis of β‐Ketoamides by Sulfonium Rearrangement
inferred← citeshttps://doi.org/10.1002/anie.202422742openalex-snapshot
Catalytic Reductive Amination and Tandem Amination–Alkylation of Esters Enabled by a Cationic Iridium Complex
inferred← citeshttps://doi.org/10.1002/anie.202425305openalex-snapshot
Isoselenourea‐Catalyzed Enantioselective Pyrazolo‐Heterocycle Synthesis Enabled by Self‐Correcting Amide and Ester Acylation
inferred← citeshttps://doi.org/10.1002/anie.202500170openalex-snapshot
Asymmetric Synthesis of S(IV)‐Stereogenic Sulfinimidate Esters by Sulfinamide Activation
inferred← citeshttps://doi.org/10.1002/anie.202508062openalex-snapshot
Total Synthesis of Isodaphlongamine H by Iridium‐Catalyzed Reductive [3 + 2] Cycloaddition of N‐ Hydroxylactam
inferred← citeshttps://doi.org/10.1002/anie.202513359openalex-snapshot
Steering Amide Synthesis from Acetonitrile by Electrochemically Derived Active Superoxide
inferred← citeshttps://doi.org/10.1002/anie.4999077openalex-snapshot
Catalytic Selective Deoxygenation and Deamination of Amides to Access Alkenes
inferred← citeshttps://doi.org/10.1002/asia.202400097openalex-snapshot
Recent Advances in NHC‐Catalyzed Chemoselective Activation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/cctc.202100672openalex-snapshot
Understanding the Structure‐Activity Relationship of Ni‐Catalyzed Amide C−N Bond Activation using Distortion/Interaction Analysis
inferred← citeshttps://doi.org/10.1002/cctc.202300715openalex-snapshot
A Co‐Ni‐CM Heterogeneous Catalyst for the Direct Synthesis of Amides from the Oxidative Coupling of Aldehydes with N‐Substituted Formamides
inferred← citeshttps://doi.org/10.1002/cctc.202402146openalex-snapshot
Photoinduced Copper‐Catalyzed Divergent Transformations of Amides via 1,5‐Hydrogen Atom Transfer
inferred← citeshttps://doi.org/10.1002/chem.202004103openalex-snapshot
Chemoselective Alpha‐Deuteration of Amides via Retro‐ene Reaction
inferred← citeshttps://doi.org/10.1002/chem.202100093openalex-snapshot
A Guide to Directing Group Removal: 8‐Aminoquinoline
inferred← citeshttps://doi.org/10.1002/chem.202203314openalex-snapshot
A Simple Four‐Step Synthesis of the Potato Alkaloid Demissidine from the Common Sapogenin Tigogenin
inferred← citeshttps://doi.org/10.1002/chem.202300191openalex-snapshot
Highly Chemoselective Synthesis of Indole Derivatives
inferred← citeshttps://doi.org/10.1002/chem.202301199openalex-snapshot
Deoxygenative Radical Boration of Inert Amides via a Combination of Relay and Cooperative Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202301729openalex-snapshot
Amide Skeletal Elongation via Amino Acid Insertion
inferred← citeshttps://doi.org/10.1002/chem.202303144openalex-snapshot
gem‐Difluoroolefination of Amides
inferred← citeshttps://doi.org/10.1002/chem.202500595openalex-snapshot
Skeletal Rearrangements of Amides via Breaking Inert Bonds
inferred← citeshttps://doi.org/10.1002/chem.202500830openalex-snapshot
Triflic Anhydride‐Mediated Synthesis of Anthraquinones and Anthrones via Unusual Intramolecular Rearrangement
inferred← citeshttps://doi.org/10.1002/chem.70919openalex-snapshot
General, Catalytic Asymmetric Reductive Alkynylation of Tertiary Aliphatic and Aromatic Amides by Cooperative Catalysis With Iridium/Copper/Carreira's PINAP
inferred← citeshttps://doi.org/10.1002/cjoc.201900035openalex-snapshot
A Stepwise Annulation for the Transformation of Cyclic Ketones to Fused 6 and 7‐Membered Cyclic Enimines and Enones
inferred← citeshttps://doi.org/10.1002/cjoc.201900215openalex-snapshot
Cross‐Coupling of Secondary Amides with Tertiary Amides: The Use of Tertiary Amides as Surrogates of Alkyl Carbanions for Ketone Synthesis
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/cjoc.202400616openalex-snapshot
Decarboxylative and Decarbonylative Borylation of Carboxylic Acids and Their Derivatives†
inferred← citeshttps://doi.org/10.1002/cjoc.202400751openalex-snapshot
Evolution of the Short Enantioselective Total Synthesis of the Unique Marine Myxobacteria Polyketide Salimabromide
inferred← citeshttps://doi.org/10.1002/cjoc.202401146openalex-snapshot
Energy Transfer‐Mediated, Triplet Excited State Proton Transfer‐Enabled Dearomatization of Indole Derivatives with Amide Functionalities
inferred← citeshttps://doi.org/10.1002/cjoc.70322openalex-snapshot
Ni/Chiral Phosphoric Acid Cooperative Catalysis Enabled Radical Coupling of Carboxylic Esters/Amides to C‐ Acyl Glycosides
inferred← citeshttps://doi.org/10.1002/cphc.201901104openalex-snapshot
How Strong is Hydrogen Bonding to Amide Nitrogen?
inferred← citeshttps://doi.org/10.1002/cplu.70159openalex-snapshot
Modular Molecular Editing for Polymer‐to‐Polymer Recycling of Postconsumer Plastics
inferred← citeshttps://doi.org/10.1002/ejoc.201900985openalex-snapshot
A Mild Synthesis of Bicyclic Alkoxyoxazolium Salts from Proline and Pipecolic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201901199openalex-snapshot
Phosphine‐Catalyzed β‐Selective Conjugate Addition of α‐Fluoro‐β‐ketoamides to Allenic Esters
inferred← citeshttps://doi.org/10.1002/ejoc.201901354openalex-snapshot
Tf2O‐Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to β‐Enaminones
inferred← citeshttps://doi.org/10.1002/ejoc.201901752openalex-snapshot
Two‐Step Catalytic Transformation of N‐Benzyllactams to Alkaloids (±)‐Solenopsin, (±)‐Solenopsin A, and (+)‐Julifloridine
inferred← citeshttps://doi.org/10.1002/ejoc.202000363openalex-snapshot
A Novel Class of 7‐Membered Heterocyclic Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.202100645openalex-snapshot
Brønsted Acid Mediated Nucleophilic Functionalization of Amides through Stable Amide C−N Bond Cleavage; One‐Step Synthesis of 2‐Substituted Benzothiazoles
inferred← citeshttps://doi.org/10.1002/ejoc.202101239openalex-snapshot
Nitroxide‐Catalyzed Oxidative Amidation of Aldehydes to Yield N‐Acyl Azoles Using Sodium Persulfate
inferred← citeshttps://doi.org/10.1002/ejoc.202200659openalex-snapshot
Selective N‐Deacetylation and Functionalization of Aminosugars
inferred← citeshttps://doi.org/10.1002/ejoc.202400297openalex-snapshot
Activation/Cyclization of 2H‐Azirines and 3‐Amino‐2‐fluoropyridines Towards 2‐Aryl‐Pyrido[2,3‐b]pyrazines
inferred← citeshttps://doi.org/10.1002/ejoc.202400898openalex-snapshot
Direct Introduction of Perfluoroacyl (−CORF) Groups into Organic Substrates
inferred← citeshttps://doi.org/10.1002/ejoc.202400905openalex-snapshot
Metal‐Free α‐(Hetero)Arylation of Amides Enabled Access to Diaryl Acetamides via Umpolung
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.70859openalex-snapshot
Practical One‐Pot Synthesis of Cyclic Conjugated Amides From Ketones
inferred← citeshttps://doi.org/10.1002/hlca.201900168openalex-snapshot
Synthesis of Benzazepinones via Intramolecular Cyclization Involving Ketene Iminium Intermediates
inferred← citeshttps://doi.org/10.1002/hlca.202400020openalex-snapshot
Nickel(II)‐Catalyzed Hydrocarbamoylation of Alkynes with Formamides towards Unsaturated Amides
inferred← citeshttps://doi.org/10.1002/slct.202100305openalex-snapshot
Triflic Anhydride (Tf 2 O): An Efficient Catalyst for Electrophilic Activation of Amides
inferred← citeshttps://doi.org/10.1002/slct.202505934openalex-snapshot
Trifluoromethanesulfonic Acid‐Promoted Esterification of Unactivated Tertiary Amides with Tetrahydrofurans and Potassium Halides to Access Haloalkyl Esters
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/tcr.202100172openalex-snapshot
Recent Progress in Enolonium Chemistry under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1007/s11030-020-10058-6openalex-snapshot
Transition metal-free NaOH-catalyzed hydration of nitriles to primary amides in NH3·H2O–DMSO mixture
inferred← citeshttps://doi.org/10.1007/s11426-019-9586-3openalex-snapshot
Amides as surrogates of aldehydes for C-C bond formation: amide-based direct Knoevenagel-type condensation reaction and related reactions
inferred← citeshttps://doi.org/10.1007/s11426-019-9665-5openalex-snapshot
Ni-catalyzed direct alcoholysis of N-acylpyrrole-type tertiary amides under mild conditions
inferred← citeshttps://doi.org/10.1007/s11426-022-1331-yopenalex-snapshot
Deoxygenative alkylation of tertiary amides using alkyl iodides under visible light
inferred← citeshttps://doi.org/10.1007/s11426-025-2935-3openalex-snapshot
Streamlined synthesis of α-keto-, α-hydroxy- and α,α-difluorophosphonates from amides via electrophilic activation with trifluoromethanesulfonic anhydride
inferred← citeshttps://doi.org/10.1007/s41061-020-00309-3openalex-snapshot
Cross-dehydrogenative Coupling Reactions Between Formamidic C(sp2)–H and X–H (X = C, O, N) Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-323-95893-6.00004-9openalex-snapshot
Visible light–driven organic synthesis under iridium (IrIII)-complex photocatalysis
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00006-0openalex-snapshot
Amides and Lactams
inferred← citeshttps://doi.org/10.1016/b978-0-443-51074-8.00015-2openalex-snapshot
Recent progress in synthesis of Solanum alkaloids of spirosolane and solanidane type
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.01.018openalex-snapshot
One-pot tandem route to fused indolizidines and quinolizidines: Application in the synthesis of alkaloids and bioactive compounds
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.110809openalex-snapshot
Mechanistic insights for Aryl dilithium base enables the acylation of unactivated Csp3H
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.217493openalex-snapshot
Toward layered double oxide-based nanomaterials: From synthesis to diverse applications
inferred← citeshttps://doi.org/10.1016/j.chempr.2019.06.008openalex-snapshot
Oxidation Stepping Stones: α-Oxytriflation Enables Asymmetric Arylation of Amides
inferred← citeshttps://doi.org/10.1016/j.chempr.2020.05.009openalex-snapshot
Hydrolysis of Twisted Amides inside a Self-Assembled Coordination Cage
inferred← citeshttps://doi.org/10.1016/j.chempr.2023.03.002openalex-snapshot
Direct enantioselective α-amination of amides guided by DFT prediction of E/Z selectivity in a sulfonium intermediate
inferred← citeshttps://doi.org/10.1016/j.ejps.2026.107572openalex-snapshot
Impact of gamma irradiation and ethylene oxide sterilisation on the stability of crystalline and amorphous drug solids
inferred← citeshttps://doi.org/10.1016/j.jechem.2026.02.031openalex-snapshot
Electrocatalytic C–N coupling of carbon dioxide and nitrogen-containing small molecules for synthesizing organic nitrogenous compounds
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.molstruc.2019.02.030openalex-snapshot
Synthesis, structural and spectroscopic features of 2,2,2-trichloro-N-[(trimethylsilyl)methyl]acetamide and 2,2,2-trimethyl-N-[(trimethylsilyl)methyl]acetamide
inferred← citeshttps://doi.org/10.1016/j.slast.2026.100450openalex-snapshot
An adaptable microplate-integrated purification workflow tailored for high-throughput automated parallel amide syntheses
inferred← citeshttps://doi.org/10.1016/j.snb.2023.134669openalex-snapshot
Liquid crystal elastomer film actuators with anti-strain robustness
inferred← citeshttps://doi.org/10.1016/j.tet.2018.12.024openalex-snapshot
Ir-catalyzed chemoselective reduction of β-amido esters: A versatile approach to β-enamino esters
inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.024openalex-snapshot
A lifetime journey into the world of chemistry
inferred← citeshttps://doi.org/10.1016/j.tet.2019.07.016openalex-snapshot
Dual demeanour of norcantharidin derived dicarboxamides in acidic media: An insight
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131754openalex-snapshot
Synthesis of cytotoxic spirocyclic imides from a biomass-derived oxanorbornene
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132148openalex-snapshot
A mild method for the replacement of a hydroxyl group by halogen: 3. the dichotomous behavior of α-haloenamines towards allylic and propargylic alcohols
inferred← citeshttps://doi.org/10.1016/j.tet.2022.132779openalex-snapshot
Interception of enamine intermediates in reductive functionalization of lactams by sodium hydride: Synthesis of 2-cyano-3-iodo piperidines and pyrrolidines
inferred← citeshttps://doi.org/10.1016/j.tet.2022.132875openalex-snapshot
Anion binding by receptors containing NH donating groups – What do anions prefer?
inferred← citeshttps://doi.org/10.1016/j.tet.2022.132935openalex-snapshot
A flexible enantioselective approach to 2,5-disubstituted cis-decahydroquinolines
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134632openalex-snapshot
Catalyst- and solvent-free hydrosulfonylation of alkenes with sulfinates enabling green synthesis of β-sulfonyl amides
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134986openalex-snapshot
Hexaniobate-based catalytic system for the hydration of nitriles and one-pot cascade synthesis of 2-substituted quinazolinones from 2-aminobenzonitriles and alcohols in water medium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153731openalex-snapshot
De novo synthesis of polysubstituted β-naphthylamines via Tf2O-mediated [4+2] annulation of amides with alkynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154831openalex-snapshot
An unexpected side reaction in the transformation of an alcohol to an amine facilitated by triflic anhydride-pyridine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154887openalex-snapshot
Direct amidation of 1-aryl-2,2,2-trifluoroethanones with isothiocyanates via C–C bond cleavage strategy
inferred← citeshttps://doi.org/10.1016/j.xcrp.2022.100955openalex-snapshot
Efficient synthesis of β-substituted amines via combining deoxygenation of amides with photochemical organocatalysis
inferred← citeshttps://doi.org/10.1016/j.xcrp.2022.101116openalex-snapshot
Incorporation of germanium into amines via deoxygenative germylation of aromatic amides with hydrogermanes
inferred← citeshttps://doi.org/10.1016/j.xcrp.2023.101574openalex-snapshot
Heteroaromatization and nickel catalysis enabled decarbamoylative arylations and borylations of tertiary amides
inferred← citeshttps://doi.org/10.1016/s1872-2067(21)63853-6openalex-snapshot
Zirconium-hydride-catalyzed site-selective hydroboration of amides for the synthesis of amines: Mechanism, scope, and application
inferred← citeshttps://doi.org/10.1021/acs.accounts.3c00171openalex-snapshot
New Strategies for the Functionalization of Carbonyl Derivatives via α-Umpolung: From Enolates to Enolonium Ions
inferred← citeshttps://doi.org/10.1021/acs.accounts.4c00549openalex-snapshot
[Pd(NHC)(μ-Cl)Cl]2: The Highly Reactive Air- and Moisture-Stable, Well-Defined Pd(II)-N-Heterocyclic Carbene (NHC) Complexes for Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00225openalex-snapshot
Acyclic Twisted Amides
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02015openalex-snapshot
General Synthesis of Fully Substituted 4-Aminooxazoles from Amides and 1,4,2-Dioxazol-5-ones Based on Amide Activation and Umpolung Process
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02148openalex-snapshot
Synthesis of Imidazo[1,2-a]pyridines: Triflic Anhydride-Mediated Annulation of 2H-Azirines with 2-Chloropyridines
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02843openalex-snapshot
Iron-Catalyzed Cycloaddition of Amides and 2,3-Diaryl-2H-azirines To Access Oxazoles via C–N Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02868openalex-snapshot
Amide/Ester Cross-Coupling via C–N/C–H Bond Cleavage: Synthesis of β-Ketoesters
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02929openalex-snapshot
Chemoselective Reactions of Isocyanates with Secondary Amides: One-Pot Construction of 2,3-Dialkyl-Substituted Quinazolinones
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01110openalex-snapshot
Evaluation of Cyclic Amides as Activating Groups in N–C Bond Cross-Coupling: Discovery of N-Acyl-δ-valerolactams as Effective Twisted Amide Precursors for Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01543openalex-snapshot
Bischler–Napieralski Synthesis of 6-Alkynyl Phenanthridines Based on Tf2O-Promoted Electrophilic Activation of N-Aryl-2-propynamides
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01572openalex-snapshot
Tf2O/TTBP (2,4,6-Tri-tert-butylpyrimidine): An Alternative Amide Activation System for the Direct Transformations of Both Tertiary and Secondary Amides
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02077openalex-snapshot
A CO 2 -Catalyzed Transamidation Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02835openalex-snapshot
KOtBu-Mediated Reductive Cyanation of Tertiary Amides for Synthesis of α-Aminonitriles
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02918openalex-snapshot
Bischler–Napieralski Synthesis of Polycyclic N-Heteroaromatics Based on Tf2O-Promoted Electrophilic Activation of N-Aryl-2-Propynamides
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00131openalex-snapshot
Asymmetric Synthesis of Propargylic α-Stereogenic Tertiary Amines by Reductive Alkynylation of Tertiary Amides Using Ir/Cu Tandem Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01094openalex-snapshot
Classes of Amides that Undergo Selective N–C Amide Bond Activation: The Emergence of Ground-State Destabilization
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02504openalex-snapshot
Tandem Synthesis of 2-Azaspiro[4.5]deca-1,6,9-trien-8-ones Based on Tf2O-Promoted Activation of N-(2-Propyn-1-yl) Amides
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02995openalex-snapshot
B2(OH)4-Mediated Reductive Transamidation of N-Acyl Benzotriazoles with Nitro Compounds En Route to Aqueous Amide Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00172openalex-snapshot
Structure and Additive-free Transamidation of Planar N-Cyano Amides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00477openalex-snapshot
Synthesis of Aryl Amides from Acyl-Bunte Salts and Aryl Azides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00912openalex-snapshot
Suzuki–Miyaura Cross-Coupling of Amides by N–C Cleavage Mediated by Air-Stable, Well-Defined [Pd(NHC)(sulfide)Cl2] Catalysts: Reaction Development, Scope, and Mechanism
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02095openalex-snapshot
Chemoselectivity of the CuAAC/Ring Cleavage/Cyclization Reaction between Enaminones and α-Acylketenimine
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02108openalex-snapshot
Tf 2 O-Mediated Tandem Reaction of Enaminones for the Synthesis of Functionalized Conjugated-Enals/β-Naphthalaldehydes
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00103openalex-snapshot
[(NHC)Pd(OAc)2]: Highly Active Carboxylate Pd(II)–NHC (NHC = N-Heterocyclic Carbene) Precatalysts for Suzuki–Miyaura and Buchwald–Hartwig Cross-Coupling of Amides by N–C(O) Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00246openalex-snapshot
Synthesis of Amides via the Amination of Aldehydes with Hydroxylamines Promoted by TBAF·3H 2 O
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00731openalex-snapshot
Triflic Acid-Promoted 1,2-Amino Migration Reactions in α-Arylaminoacrylamides: Access to Substituted β-Aminoamides
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01603openalex-snapshot
Divergent Synthesis of Enynals and Dihydrobenzo[ f ]isoquinolines via Deoxyalkynylation of Enaminones Enabled by the Cooperative Action of Tf 2 O/Pd/Cu
inferred← citeshttps://doi.org/10.1021/acs.joc.4c03176openalex-snapshot
HFIP-Promoted Aromatic Electrophilic Amidation of Indoles and Pyrroles with Isocyanates
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01520openalex-snapshot
Expeditious Synthesis of Chiral Imidazolidines and 1,2-Diamines via Photocatalytic [3 + 2] Cycloaddition of Chiral Sulfinamides with Azomethine Ylides
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01644openalex-snapshot
Efficient Synthesis of Amides through Thioacids Reactions with In Situ Generated Formamidine
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