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Novel Amine Chemistry Based on DMAP-Catalyzed Acylation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Encyclopedia of Reagents for Organic Synthesis
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4-Dialkylaminopyridine als hochwirksame Acylierungskatalysatoren
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Eine bequeme Methode zur Herstellung von 1‐(tert‐Butoxycarbonyl)pyrrolen
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Erschöpfende tert‐Butoxycarbonylierung von Peptid‐Stickstoffatomen
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Synthese und Eigenschaften von Nα‐Di‐tert‐butoxycarbonyl‐ und Nα‐Benzyloxycarbonyl‐tert‐butoxycarbonylaminosäuren
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Ein prototypisches Reagens für die Synthese substituierter Hydrazine
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Stereoselektive Synthese eines C‐glycosidischen Analogons des N‐Glucoasparagins
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N‐Acetylierung substituierter Pyrrole
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Protective groups in organic synthesis
inferredcites →https://doi.org/10.1016/0040-4039(95)01931-7openalex-snapshot
Substrate acidities and conversion times for reactions of amides with di-tert-butyl bicarbonate
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A highly selective protocol for the deprotection of BOC-protected amides and carbamates
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Mitsunobu reactions of n-alkyl and n-acyl sulfonamides-an efficient route to protected amines
inferredcites →https://doi.org/10.1021/jm00361a018openalex-snapshot
Synthesis and antiviral activity of distamycin A analogs: substitutions on the different pyrrole nitrogens and in the amidine function
inferredcites →https://doi.org/10.1021/jo00018a059openalex-snapshot
Di-tert-butyl N-acylimidodicarbonates as isolable acylating agents: mild conversion of primary carboxamides to substituted amides
inferredcites →https://doi.org/10.1021/jo00162a028openalex-snapshot
A mild two-step method for the hydrolysis of lactams and secondary amides
inferredcites →https://doi.org/10.1021/jo00251a035openalex-snapshot
An efficient, palladium-catalyzed route to protected allylic amines
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Synthesis of dl-gabaculine utilizing direct allylic amination as the key step
inferredcites →https://doi.org/10.1021/jo00406a023openalex-snapshot
Synthetic and kinetic studies on tricarbonates and dicarbonates
inferredcites →https://doi.org/10.1021/jo01033a003openalex-snapshot
New Methods of Introducing the Carbo-t-butoxy Amino-Protecting Group. Preparation and Use of t-Butyl Cyanoformate and t-Butyl Iminodicarboxylate1
inferredcites →https://doi.org/10.1021/jo01298a073openalex-snapshot
The chemistry of naturally occurring polyamines. 1. Total synthesis of celacinnine, celabenzine and maytenine
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A Mild Amide to Carbamate Transformation
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Direct synthesis of N-protected chiral amino acids from imidodicarbonates employing either Mitsunobu or triflate alkylation. Feasibility study using lactate with particular reference to 15N-labelling
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Synthesis of amino acid derivatives substituted in the backbone with stable isotopes for application in peptide synthesis
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Isocyanates, Part 2.7 Synthesis of Symmetrical and Unsymmetrical Ureas by DMAP-Catalyzed Reaction of Alkyl- and Arylamines with Di-tert-butyldicarbonate
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Synthesis and use of benzyl tert-butyl iminodicarbonate, a versatile reagent for the preparation of amines
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Chemoselective Substitution in 4-Toluenesulfonamides and Carbamates by Di-tert-butyl Dicarbonate in the Presence of 4-Dimethylaminopyridine.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Preparation, Isolation and Characterization of In-Situ Formed Lewis Base Adducts (Lbas) of Dbu. Their Application as Green Reagents
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Preparation, Isolation and Characterization of In-Situ Formed Lewis Base Adducts (Lbas) of Dbu. Their Application as Green Reagents
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Synthetic Chemistry: Formation of the Amide Bond
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Protection for the Amino Group
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Protection for the Amino Group
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Anhydride Activation by 4‐Dialkylaminopyridines and Analogs (n → π*)
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Nucleophile Katalyse durch 4‐(Dialkylamino)pyridine neu aufgerollt: Optimierung von Reaktivität und Selektivität
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Fluorous 4‐N,N‐Dimethylaminopyridine (DMAP) Salts as Simple Recyclable Acylation Catalysts
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Direct Hydrogenation of Nitroaromatics and One‐Pot Amidation with Carboxylic Acids over Platinum Nanowires
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ChemInform Abstract: Novel Amine Chemistry Based on DMAP‐Catalyzed Acylation
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Experiments related to the synthesis and analysis of a hydrazine library †
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Synthesis of C2-symmetric analogues of 4-(pyrrolidino)pyridine: new chiral nucleophilic catalysts
inferred← citeshttps://doi.org/10.1039/b010091aopenalex-snapshot
Synthetic methodology for alkyl substituted hydrazines
inferred← citeshttps://doi.org/10.1039/b103385aopenalex-snapshot
Atropisomeric α-methyl substituted analogues of 4-(dimethylamino)pyridine: synthesis and evaluation as acyl transfer catalysts
inferred← citeshttps://doi.org/10.1039/b506344bopenalex-snapshot
Catalytic phosphorylation using a bifunctional imidazole derived nucleophilic catalyst
inferred← citeshttps://doi.org/10.1039/b604632kopenalex-snapshot
Asymmetric acyl-transfer promoted by readily assembled chiral 4-N,N-dialkylaminopyridine derivatives
inferred← citeshttps://doi.org/10.1039/b605170gopenalex-snapshot
First C-3 lithiation of DMAP: a new entry into chemical tuning of acylation catalysts
inferred← citeshttps://doi.org/10.1039/b610140bopenalex-snapshot
Stacking interactions as the principal design element in acyl-transfer catalysts
inferred← citeshttps://doi.org/10.1039/b913515dopenalex-snapshot
Highly efficient chemoselective N-acylation with water microreaction system in the absence of catalyst
inferred← citeshttps://doi.org/10.1039/c3qo00045aopenalex-snapshot
Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines
inferred← citeshttps://doi.org/10.1039/c4ob01931hopenalex-snapshot
Oxidative activation of dihydropyridine amides to reactive acyl donors
inferred← citeshttps://doi.org/10.1039/c4qo00210eopenalex-snapshot
Enantioselective allylic amination of MBH carbonates catalyzed by novel chiral 4-dialkylaminopyridine catalysts
inferred← citeshttps://doi.org/10.1039/c4ra00131aopenalex-snapshot
DMAP-promoted domino annulation of β-ketothioamides with internal alkynes: a highly regioselective access to functionalized 1,3-thiazolidin-4-ones at room temperature
inferred← citeshttps://doi.org/10.1039/c5cc04630kopenalex-snapshot
A near infrared colorimetric and fluorometric probe for organophosphorus nerve agent mimics by intramolecular amidation
inferred← citeshttps://doi.org/10.1039/c5nj01810bopenalex-snapshot
Serendipitous discovery of an efficient method for the synthesis of dimeric-RGD analogues using DMAP-photoirradiation
inferred← citeshttps://doi.org/10.1039/c5sc02949jopenalex-snapshot
A flexible approach to Pd-catalyzed carbonylations via aroyl dimethylaminopyridinium salts
inferred← citeshttps://doi.org/10.1039/c6py00231eopenalex-snapshot
An epoxy thiolactone on stage: four component reactions, synthesis of poly(thioether urethane)s and the respective hydrogels
inferred← citeshttps://doi.org/10.1039/d0ob00734jopenalex-snapshot
Minimizing solvent waste in catalytic reactions in highly recyclable hydrocarbon solvents
inferred← citeshttps://doi.org/10.1039/d0ob01893gopenalex-snapshot
Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
inferred← citeshttps://doi.org/10.1039/d1ob01630jopenalex-snapshot
Enhancing catalytic activity of pyridines via para -iminophosphorano substituents
inferred← citeshttps://doi.org/10.1039/d4cc03521fopenalex-snapshot
One-pot synthesis of functionalized dihydropyridin-2-ones via carbene-catalyzed base-controlled [3+3] annulation reaction
inferred← citeshttps://doi.org/10.1039/d4dt01399aopenalex-snapshot
Electron-rich pyridines with para -N-heterocyclic imine substituents: ligand properties and coordination to CO 2 , SO 2 , BCl 3 and Pd II complexes
inferred← citeshttps://doi.org/10.1039/d4ra04548copenalex-snapshot
Synthesis and evaluation of sulfonamide derivatives of quinoxaline 1,4-dioxides as carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1039/d5ce00604jopenalex-snapshot
π-Stacked organic frameworks with captured ammonia for benzamide synthesis
inferred← citeshttps://doi.org/10.1039/d5ta10389dopenalex-snapshot
Rational embedding of DMAP into covalent triazine frameworks for efficient heterogeneous organocatalysis
inferred← citeshttps://doi.org/10.1080/00304940009355935openalex-snapshot
ASYMMETRIC CATALYSIS OF ACYL TRANSFER BY LEWIS ACIDS AND NUCLEOPHILES. A REVIEW
inferred← citeshttps://doi.org/10.1080/00397911.2011.565453openalex-snapshot
Simple and Effective Synthetic Approach to Chiral 2-Amino-4-piperidinyl Pyridine Derivatives
inferred← citeshttps://doi.org/10.1134/s1070363217090109openalex-snapshot
Chemoselective acylation of monosubstituted thiacalix[4]arene with di-tert-butyl dicarbonate
inferred← citeshttps://doi.org/10.1135/cccc2008164openalex-snapshot
Evidence for general base catalysis by protic solvents in a kinetic study of alcoholyses and hydrolyses of 1-(phenoxycarbonyl)pyridinium ions under both solvolytic and non-solvolytic conditions
inferred← citeshttps://doi.org/10.19261/cjm.2019.639openalex-snapshot
Multi-component Reaction Synthesis of 1,6-diamino-2-oxo-1,2,3,4-tetrahydropyridine-3,5-dicarbonitriles Using Ultrasonication and Dmap as Catalyst
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3933525/v1openalex-snapshot
Preparation, Isolation and Structural Characterization of Transient Species of DBU. Their Application as Green Reagents
inferred← citeshttps://doi.org/10.31351/vol27iss1pp100-108openalex-snapshot
Synthesis, Characterization and Alpha Glucosidase Inhibition activity of new Phthalimide Derivatives
inferred← citeshttps://doi.org/10.3184/030823401103169658openalex-snapshot
Hydrogen-Bonded (H 2 O·X) 2 [X=Cl – , Br – ] Clusters in 1-Phenacyl-4-(Dimethylamino)Pyridinium Halide Monohydrates
inferred← citeshttps://doi.org/10.3389/fchem.2020.622867openalex-snapshot
Copper(II)-Dioxygen Facilitated Activation of Nitromethane: Nitrogen Donors for the Synthesis of Substituted 2-Hydroxyimino-2-phenylacetonitriles and Phthalimides
inferred← citeshttps://doi.org/10.3390/molecules26061813openalex-snapshot
Selective Synthesis of N-Acylnortropane Derivatives in Palladium-Catalysed Aminocarbonylation
inferred← citeshttps://doi.org/10.3390/polym12112526openalex-snapshot
Constructing Positively Charged Thin-Film Nanocomposite Nanofiltration Membranes with Enhanced Performance
inferred← citeshttps://doi.org/10.3987/com-06-10748openalex-snapshot
Synthesis of 4-(Dimethylamino)pyridinium-substituted Pyrazine, Pyridazine, 1,3,5-Triazine, Purine, and Imidazole
inferred← citeshttps://doi.org/10.3987/com-12-s(n)1openalex-snapshot
A Diversified Approach to the Synthesis of Highly Functionalized Novel Azines and Azoles from 2H-Pyran-2-ones
inferred← citeshttps://doi.org/10.3987/com-13-12818openalex-snapshot
Efficient Organocatalytic Michael Addition Reaction of β−Ketoesters under High Pressure
inferred← citeshttps://doi.org/10.3998/ark.5550190.0002.114openalex-snapshot
Catalysis by 4-dialkylaminopyridines
inferred← citeshttps://doi.org/10.70675/534df6a3z6dc9z43a1z8757z35b647173204openalex-snapshot
Formation de liaisons amides par réactions enzymatiques détournées
inferred← citeshttps://doi.org/10.9734/irjpac/2016/27469openalex-snapshot
Chronological Review of the Catalytic Progress of Polylactic Acid Formation through Ring Opening Polymerization
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