On the public citation graph
An Efficient Synthesis of Enamides from Ketones
0 signed · 97 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adsc.200390000openalex-snapshot
Selective Hydrogenation for Fine Chemicals: Recent Trends and New Developments
inferredcites →https://doi.org/10.1016/0040-4039(96)00078-0openalex-snapshot
A new selective reduction of nitroalkenes into enamides
inferredcites →https://doi.org/10.1016/j.tet.2004.03.004openalex-snapshot
A new highly chemoselective isomerization of allylamides
inferredcites →https://doi.org/10.1016/j.tetlet.2004.10.063openalex-snapshot
A complementary method to obtain N-acyl enamides using the Heck reaction: extending the substrate scope for asymmetric hydrogenation
inferredcites →https://doi.org/10.1016/s0040-4039(00)88913-3openalex-snapshot
A new and mild procedure for the preparation of vinyl formamides from thiooximes
inferredcites →https://doi.org/10.1021/jo9809332openalex-snapshot
A Three-Step Procedure for Asymmetric Catalytic Reductive Amidation of Ketones
inferredcites →https://doi.org/10.1021/jo981590aopenalex-snapshot
Practical Syntheses of β-Amino Alcohols via Asymmetric Catalytic Hydrogenation
inferredcites →https://doi.org/10.1021/ol005800topenalex-snapshot
Synthesis of Enamides Related to the Salicylate Antitumor Macrolides Using Copper-Mediated Vinylic Substitution
inferredcites →https://doi.org/10.1021/ol035355copenalex-snapshot
Copper-Catalyzed Coupling of Amides and Carbamates with Vinyl Halides
inferredcites →https://doi.org/10.1021/ol035959gopenalex-snapshot
Palladium-Catalyzed Amidation of Enol Triflates: A New Synthesis of Enamides
inferredcites →https://doi.org/10.1021/ol036381dopenalex-snapshot
Divergent and Stereocontrolled Synthesis of the Enamide Side Chains of Oximidines I/II/III, Salicylihalamides A/B, Lobatamides A/D, and CJ-12,950
inferredcites →https://doi.org/10.1021/ol0494360openalex-snapshot
Formation of Enamides via Palladium(II)-Catalyzed Vinyl Transfer from Vinyl Ethers to Nitrogen Nucleophiles
inferredcites →https://doi.org/10.1021/ol050117yopenalex-snapshot
Preparation of Enamides via Palladium-Catalyzed Amidation of Enol Tosylates
inferredcites →https://doi.org/10.1021/ol061318kopenalex-snapshot
Direct N-Acetyl Enamine Formation: Lithium Bromide Mediated Addition of Methyllithium to Nitriles
inferredcites →https://doi.org/10.1055/s-1999-2937openalex-snapshot
Optically Active Amine Derivatives: Ruthenium-Catalyzed Enantioselective Hydrogenation of Enamides
inferredcites →https://doi.org/10.1055/s-2005-918480openalex-snapshot
Efficient Palladium-Catalysed Enamide Synthesis from Enol Triflates and Enol Tosylates
inferredcites →https://doi.org/10.1246/cl.1991.1443openalex-snapshot
Stereospecific One-pot Synthesis of Enamides and Enimides by the Copper Iodide Promoted Vinylic Substitution
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/0471264229.os087.30openalex-snapshot
Synthesis of Enamides from Ketones: Preparation of N ‐(3,4‐Dihydronaphthalene‐1‐Yl)Acetamide
inferred← citeshttps://doi.org/10.1002/0471264229.os090.06openalex-snapshot
Synthesis of N ‐Acetyl Enamides by Reductive Acetylation of Oximes Mediated with Iron( II ) Acetate: N ‐(1‐(4‐Bromophenyl)vinyl)acetamide
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11442.pub2openalex-snapshot
Trialkylphosphines
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11442.pub3openalex-snapshot
Trialkylphosphines
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11442.pub4openalex-snapshot
Trialkylphosphines
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11442.pub5openalex-snapshot
Trialkylphosphines
inferred← citeshttps://doi.org/10.1002/9783527629541.ch9openalex-snapshot
Bidentate Ligands for Enantioselective Enamide Reduction
inferred← citeshttps://doi.org/10.1002/9783527630639.ch20openalex-snapshot
Enabling Asymmetric Hydrogenation for the Design of Efficient Synthesis of Drug Substances
inferred← citeshttps://doi.org/10.1002/9783527633562.ch9openalex-snapshot
CB1R Inverse Agonist – Taranabant
inferred← citeshttps://doi.org/10.1002/adsc.200900719openalex-snapshot
Chiral Amine Synthesis – Recent Developments and Trends for Enamide Reduction, Reductive Amination, and Imine Reduction
inferred← citeshttps://doi.org/10.1002/adsc.201400584openalex-snapshot
Exploiting the Nucleophilicity of NH Imines: Synthesis of Enamides from Alkyl Azides and Acid Anhydrides
inferred← citeshttps://doi.org/10.1002/ange.200805058openalex-snapshot
Efficient Synthesis of Chiral β‐Arylisopropylamines by Using Catalytic Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/ange.201107601openalex-snapshot
Direct Titanium‐Mediated Conversion of Ketones into Enamides with Ammonia and Acetic Anhydride
inferred← citeshttps://doi.org/10.1002/anie.200805058openalex-snapshot
Efficient Synthesis of Chiral β‐Arylisopropylamines by Using Catalytic Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/anie.201107601openalex-snapshot
Direct Titanium‐Mediated Conversion of Ketones into Enamides with Ammonia and Acetic Anhydride
inferred← citeshttps://doi.org/10.1002/asia.202300678openalex-snapshot
Direct Synthesis of Aldoximes: Ruthenium‐Catalyzed Coupling of Alcohols and Hydroxylamine Hydrochloride
inferred← citeshttps://doi.org/10.1002/cctc.201500935openalex-snapshot
Synthesis of Enamides by Ruthenium‐Catalyzed Reaction of Alkyl Azides with Acid Anhydrides in Ionic Liquid
inferred← citeshttps://doi.org/10.1002/cctc.201900132openalex-snapshot
Phosphite‐thioether/selenoether Ligands from Carbohydrates: An Easily Accessible Ligand Library for the Asymmetric Hydrogenation of Functionalized and Unfunctionalized Olefins
inferred← citeshttps://doi.org/10.1002/chem.201003265openalex-snapshot
Synthesis of 1,2‐Amino Alcohols by Sigmatropic Rearrangements of 3‐(N‐Tosylamino)allylic Alcohol Derivatives
inferred← citeshttps://doi.org/10.1002/chem.201904596openalex-snapshot
Fused N‐Heterocycles with Contiguous Stereogenic Centers Accessed by an Asymmetric Catalytic Cascade Reaction of Tertiary Enamides
inferred← citeshttps://doi.org/10.1002/chin.200827068openalex-snapshot
ChemInform Abstract: An Efficient Synthesis of Enamides from Ketones.
inferred← citeshttps://doi.org/10.1002/ejoc.201600638openalex-snapshot
The Synthesis of Ketone‐Derived Enamides by Elimination of HCN from Cyanoamides
inferred← citeshttps://doi.org/10.1002/hlca.201200175openalex-snapshot
Metal‐Free 2,2,6,6‐Tetramethylpiperidin‐1‐yloxy Radical (TEMPO) Catalyzed Aerobic Oxidation of Hydroxylamines and Alkoxyamines to Oximes and Oxime Ethers
inferred← citeshttps://doi.org/10.1002/poc.4165openalex-snapshot
Stereoelectronic effects: Perlin effects in cyclohexane‐derived compounds
inferred← citeshttps://doi.org/10.1002/slct.201800032openalex-snapshot
Aqueous Chloroplatinic Acid: A Green, Chemoselective and Reusable Catalyst for the Deprotection of Acetals, Ketals, Dioxolanes and Oxathiolanes
inferred← citeshttps://doi.org/10.1002/slct.201803927openalex-snapshot
PhI(OAc) 2 ‐Mediated One‐Pot Synthesis and their Antibacterial Activity of Flavone and Coumarin Based Isoxazoles Under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1002/zaac.201200454openalex-snapshot
Introducing a New Naphthoxime‐based Ligand into the Chemistry of Triangular [Mn3] Complexes
inferred← citeshttps://doi.org/10.1007/3418_2012_57openalex-snapshot
Metal-Catalyzed C(sp2)–N Bond Formation
inferred← citeshttps://doi.org/10.1007/978-3-642-33173-2_2openalex-snapshot
The Synthesis of Novel Dihydronaphthalenes and Benzofluorenes
inferred← citeshttps://doi.org/10.1007/s00044-013-0871-2openalex-snapshot
Synthesis and anticonvulsant evaluation of some new 1,3,4,5-tetrahydro-6-alkoxy-2H-1-benzazepin-2-one derivatives
inferred← citeshttps://doi.org/10.1007/s11094-022-02617-yopenalex-snapshot
Synthesis and Biological Activity of Morita Baylis Hillman Adducts and their Oximes
inferred← citeshttps://doi.org/10.1016/j.electacta.2010.09.063openalex-snapshot
Study on the oxidation of C4-phenolic-1,4-dihydropyridines and its reactivity towards superoxide radical anion in dimethylsulfoxide
inferred← citeshttps://doi.org/10.1016/j.forc.2024.100558openalex-snapshot
Forensic implications of novel synthesis of cathinone derivatives by Neber and modified Neber rearrangements
inferred← citeshttps://doi.org/10.1016/j.mencom.2015.03.003openalex-snapshot
Syntheses of α-cyano substituted oximes from terpenic hydrocarbons via nitroso chlorides: X-ray structures of 3-cyanocaran-4-one oxime, 2-cyanopinan-3-one oxime and 1-cyano-p-menth-8-en-2-one oxime
inferred← citeshttps://doi.org/10.1016/j.tet.2010.07.048openalex-snapshot
Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2012.10.027openalex-snapshot
An efficient preparation of N-acetyl enamides catalyzed by Ru(II) complexes
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133010openalex-snapshot
NaNO2/K2S2O8-mediated selective transformation of 3-formylchromones to 2-hydroxyiminobenzofuran-3-ones and 2-alkoxy-3-(hydroxyimino)chromanones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.08.077openalex-snapshot
Isoquinoline skeleton synthesis via chelation-assisted C−H activation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.05.006openalex-snapshot
Efficient and practical synthesis of N-acetyl enamides from ketoximes by unique iron catalytic system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154799openalex-snapshot
Iodine catalyzed one-pot three-step synthesis of isoxazoles from primary alcohols and 3-O-propargyl flavones using DMSO as the oxidant
inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60220-5openalex-snapshot
One-pot green synthesis of enamides and 1,3-diynes
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01926openalex-snapshot
Unlock the C–N Bond Amidation of Enaminones: Metal-Free Synthesis of Enamides by Water-Assisted Transamidation
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00889openalex-snapshot
Axially Chiral Enamides: Substituent Effects, Rotation Barriers, and Implications for their Cyclization Reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02983openalex-snapshot
Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00911openalex-snapshot
Palladium-Catalyzed Regioselective [3 + 2] Annulation with N-Allenamides at the Proximal C═C Bond: Synthesis of γ-Amino-α′-methylenecyclopentenones
inferred← citeshttps://doi.org/10.1021/acscatal.9b04699openalex-snapshot
Palladium-Catalyzed Dual Ligand-Enabled Alkylation of Silyl Enol Ether and Enamide under Irradiation: Scope, Mechanism, and Theoretical Elucidation of Hybrid Alkyl Pd(I)-Radical Species
inferred← citeshttps://doi.org/10.1021/acsomega.3c06619openalex-snapshot
Inhibitory Effects of B-, C-, and E-Ring-Truncated Deguelin Derivatives Against A549, HCT116, and MCF-7 Cancer Cells
inferred← citeshttps://doi.org/10.1021/cs500261kopenalex-snapshot
Rhodium-Catalyzed Asymmetric Hydrogenation of β-Acetylamino Acrylosulfones: A Practical Approach to Chiral β-Amido Sulfones
inferred← citeshttps://doi.org/10.1021/jacs.7b07347openalex-snapshot
Selective Synthesis of Primary Anilines from Cyclohexanone Oximes by the Concerted Catalysis of a Mg–Al Layered Double Hydroxide Supported Pd Catalyst
inferred← citeshttps://doi.org/10.1021/jo1022348openalex-snapshot
Synthesis of Enamides via CuI-Catalyzed Reductive Acylation of Ketoximes with NaHSO3
inferred← citeshttps://doi.org/10.1021/jo302073eopenalex-snapshot
Synthesis of Oxazoles from Enamides via Phenyliodine Diacetate-Mediated Intramolecular Oxidative Cyclization
inferred← citeshttps://doi.org/10.1021/jo902177popenalex-snapshot
Regioselective Synthesis of Heterocycles Containing Nitrogen Neighboring an Aromatic Ring by Reductive Ring Expansion Using Diisobutylaluminum Hydride and Studies on the Reaction Mechanism
inferred← citeshttps://doi.org/10.1021/jo902259uopenalex-snapshot
A Facile and Practical Synthesis of N-Acetyl Enamides
inferred← citeshttps://doi.org/10.1021/ol102504bopenalex-snapshot
Rhodium(III)-Catalyzed Synthesis of Isoquinolines from Aryl Ketone O-Acyloxime Derivatives and Internal Alkynes
inferred← citeshttps://doi.org/10.1021/ol800996jopenalex-snapshot
A Convenient Synthesis and the Asymmetric Hydrogenation of N-Phthaloyl Dehydroamino Acid Esters
inferred← citeshttps://doi.org/10.1021/ol802482dopenalex-snapshot
A Facile Deprotection of Secondary Acetamides
inferred← citeshttps://doi.org/10.1021/ol802665vopenalex-snapshot
Synthesis of Enamides via Rh/C-Catalyzed Direct Hydroacylation of Ketoximes
inferred← citeshttps://doi.org/10.1021/op400055zopenalex-snapshot
The P-Chiral Phosphane Ligand (MeO-BIBOP) for Efficient and Practical Large-Scale Rh-Catalyzed Asymmetric Hydrogenation of N-Acetyl Enamides with High TONs
inferred← citeshttps://doi.org/10.1021/op800270eopenalex-snapshot
New Efficient Asymmetric Synthesis of Taranabant, a CB1R Inverse Agonist for the Treatment of Obesity
inferred← citeshttps://doi.org/10.1039/b809319aopenalex-snapshot
Enamides: valuable organic substrates
inferred← citeshttps://doi.org/10.1039/b910757fopenalex-snapshot
Geometry-dependent divergence in the gold-catalyzed redox cascade cyclization of o-alkynylaryl ketoximes and nitrones leading to isoindoles
inferred← citeshttps://doi.org/10.1039/c2cs15312bopenalex-snapshot
Asymmetric homogeneous hydrogenations at scale
inferred← citeshttps://doi.org/10.1039/c3ob41847bopenalex-snapshot
Metal free stereoselective synthesis of functionalized enamides
inferred← citeshttps://doi.org/10.1039/c3ra42088dopenalex-snapshot
Recent advances in stoichiometric phosphine-mediated organic synthetic reactions
inferred← citeshttps://doi.org/10.1039/c6gc02156eopenalex-snapshot
Brønsted acid catalyzed transoximation reaction: synthesis of aldoximes and ketoximes without use of hydroxylamine salts
inferred← citeshttps://doi.org/10.1039/c7qo00729aopenalex-snapshot
Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides
inferred← citeshttps://doi.org/10.1039/c8qo01353eopenalex-snapshot
Recent advances in photocatalytic C–S/P–S bond formation via the generation of sulfur centered radicals and functionalization
inferred← citeshttps://doi.org/10.1039/c9md00127aopenalex-snapshot
Synthesis and biological evaluation of structurally diverse α-conformationally restricted chalcones and related analogues
inferred← citeshttps://doi.org/10.1039/d5gc05558jopenalex-snapshot
Palladium-catalyzed asymmetric sequential hydroalkylation and hydroamination of 1,3-enynes with 3-hydroxyindoles
inferred← citeshttps://doi.org/10.1080/00397911.2012.666314openalex-snapshot
Efficient Synthesis of Isoquinoline Derivatives via AgOTf/Cu(OTf)2-Cocatalyzed Cyclization of 2-Alkynyl Benzaldoxime
inferred← citeshttps://doi.org/10.1080/00397911.2022.2076246openalex-snapshot
Efficient synthesis of β-(diphenylphosphoryl)- and β-(diphenylphosphorothioyl)-enamides via copper(I)-catalyzed reductive acylation of β-phosphonyloximes with KSCN as the terminal reductant
inferred← citeshttps://doi.org/10.2494/photopolymer.33.269openalex-snapshot
Synthesis and Photo-degradation of Polyphthalaldehydes with Oxime Ether Terminals
inferred← citeshttps://doi.org/10.31274/td-20240329-213openalex-snapshot
Design and synthesis of efficient BODIPY-based photochemical tools for drug delivery and imaging
inferred← citeshttps://doi.org/10.3987/com-08-11629openalex-snapshot
Regiospecific Synthesis of Unsubstituted Basic Skeletons of Heterocycles Containing Nitrogen Neighboring an Aromatic Ring by the Reductive Ring Expansion Reaction Using Diisobutylaluminum Hydride
inferred← citeshttps://doi.org/10.70675/0530eba3z4f4fz4ad3z889bz0213651d162eopenalex-snapshot
Synthèse et application de synthons originaux de type 2-aminoacrylonitriles
inferred← citeshttps://doi.org/10.70675/43ee5c50zef1fz41a9zb6fcza8c1aacdc9edopenalex-snapshot
Conjugated molecules for the elaboration of optical sensors for water monitoring
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.