On the public citation graph

Direct Catalytic Desaturation of Lactams Enabled by Soft Enolization

0 signed · 144 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ange.201601559openalex-snapshot
Chiral Nanoparticles/Lewis Acids as Cooperative Catalysts for Asymmetric 1,4‐Addition of Arylboronic Acids to α,β‐Unsaturated Amides
inferredcites →https://doi.org/10.1002/anie.201409765openalex-snapshot
Chemical Assembly Systems: Layered Control for Divergent, Continuous, Multistep Syntheses of Active Pharmaceutical Ingredients
inferredcites →https://doi.org/10.1002/anie.201601559openalex-snapshot
Chiral Nanoparticles/Lewis Acids as Cooperative Catalysts for Asymmetric 1,4‐Addition of Arylboronic Acids to α,β‐Unsaturated Amides
inferredcites →https://doi.org/10.1002/chem.201604306openalex-snapshot
Palladium(II)‐Catalyzed Dehydroboration via Generation of Boron Enolates
inferredcites →https://doi.org/10.1002/ejoc.201000278openalex-snapshot
One‐Pot Syntheses of α,β‐Unsaturated Carbonyl Compounds through Palladium‐Mediated Dehydrogenation of Ketones, Aldehydes, Esters, Lactones and Amides
inferredcites →https://doi.org/10.1007/bf02494504openalex-snapshot
Hydroxylation of substituted diatomic phenols and their derivatives
inferredcites →https://doi.org/10.1016/b978-0-08-097742-3.00707-2openalex-snapshot
7.06 Oxidation Adjacent to CX Bonds by Dehydrogenation
inferredcites →https://doi.org/10.1016/j.tetlet.2004.11.106openalex-snapshot
One-pot dehydrogenation of carboxylic acid derivatives to α,β-unsaturated carbonyl compounds under mild conditions
inferredcites →https://doi.org/10.1016/j.tetlet.2014.09.005openalex-snapshot
Catalytic CC bond forming transformations via direct β-CH functionalization of carbonyl compounds
inferredcites →https://doi.org/10.1016/s0040-4039(00)89377-6openalex-snapshot
Verbesserte variante der knoevenagel-kondensation mit TiCl4/THF/pyridin(I). Alkyliden- und Arylidenmalonester bei 0–25°C.
inferredcites →https://doi.org/10.1021/acscatal.6b02406openalex-snapshot
Palladium-Catalyzed Aerobic Dehydrogenation of Cyclic Hydrocarbons for the Synthesis of Substituted Aromatics and Other Unsaturated Products
inferredcites →https://doi.org/10.1021/bk-2016-1236.ch004openalex-snapshot
Boron Enolate Chemistry
inferredcites →https://doi.org/10.1021/cr020022zopenalex-snapshot
Rhodium-Catalyzed Asymmetric 1,4-Addition and Its Related Asymmetric Reactions
inferredcites →https://doi.org/10.1021/ja00218a062openalex-snapshot
Silylation-mediated oxidation of 4-aza-3-ketosteroids with DDQ proceeds via DDQ-substrate adducts
inferredcites →https://doi.org/10.1021/ja00398a058openalex-snapshot
Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates
inferredcites →https://doi.org/10.1021/ja00432a034openalex-snapshot
New synthetic reactions. Sulfenylations and dehydrosulfenylations of esters and ketones
inferredcites →https://doi.org/10.1021/ja00799a062openalex-snapshot
Electrophilic and nucleophilic organoselenium reagents. New routes to .alpha.,.beta.-unsaturated carbonyl compounds
inferredcites →https://doi.org/10.1021/ja01589a035openalex-snapshot
Some Reactions of N-Acetylphthalimides
inferredcites →https://doi.org/10.1021/ja031544eopenalex-snapshot
Palladium-Catalyzed Arylation of Trimethylsilyl Enolates of Esters and Imides. High Functional Group Tolerance and Stereoselective Synthesis of α-Aryl Carboxylic Acid Derivatives
inferredcites →https://doi.org/10.1021/ja036792popenalex-snapshot
Palladium-Catalyzed α-Arylation of Esters and Amides under More Neutral Conditions
inferredcites →https://doi.org/10.1021/ja057778aopenalex-snapshot
Catalytic Four-Component Assembly Based on Allenylboronate Platform: New Access to Privileged Allylic Amine Structures
inferredcites →https://doi.org/10.1021/ja206575jopenalex-snapshot
Synthesis of Cyclic Enones via Direct Palladium-Catalyzed Aerobic Dehydrogenation of Ketones
inferredcites →https://doi.org/10.1021/ja4031648openalex-snapshot
Aerobic Dehydrogenation of Cyclohexanone to Cyclohexenone Catalyzed by Pd(DMSO) 2 (TFA) 2 : Evidence for Ligand-Controlled Chemoselectivity
inferredcites →https://doi.org/10.1021/ja410389aopenalex-snapshot
Catalytic Direct β-Arylation of Simple Ketones with Aryl Iodides
inferredcites →https://doi.org/10.1021/ja980666hopenalex-snapshot
Rhodium-Catalyzed Asymmetric 1,4-Addition of Aryl- and Alkenylboronic Acids to Enones
inferredcites →https://doi.org/10.1021/jacs.5b02243openalex-snapshot
Palladium-Catalyzed α,β-Dehydrogenation of Esters and Nitriles
inferredcites →https://doi.org/10.1021/jacs.5b12924openalex-snapshot
Amide α,β-Dehydrogenation Using Allyl-Palladium Catalysis and a Hindered Monodentate Anilide
inferredcites →https://doi.org/10.1021/jacs.6b11908openalex-snapshot
Frustrated Lewis Acid/Brønsted Base Catalysts for Direct Enantioselective α-Amination of Carbonyl Compounds
inferredcites →https://doi.org/10.1021/jm00106a024openalex-snapshot
Structure-activity relationship of quinazolinedione inhibitors of calcium-independent phosphodiesterase
inferredcites →https://doi.org/10.1021/jo00064a028openalex-snapshot
Iodotrimethylsilane-mediated 2-monohalogenation of 4-aza-5.alpha.-androstan-3-one steroids
inferredcites →https://doi.org/10.1021/jo00399a052openalex-snapshot
Synthesis of .alpha.,.beta.-unsaturated carbonyl compounds by palladium(II)-catalyzed dehydrosilylation of silyl enol ethers
inferredcites →https://doi.org/10.1021/jo00805a004openalex-snapshot
Preparation of .alpha.,.beta.-unsaturated carbonyl compunds
inferredcites →https://doi.org/10.1021/jo0103930openalex-snapshot
Rhodium-Catalyzed Asymmetric 1,4-Addition of Organoboron Reagents to 5,6-Dihydro-2(1H)-pyridinones. Asymmetric Synthesis of 4-Aryl-2-piperidinones
inferredcites →https://doi.org/10.1021/jo0484880openalex-snapshot
Synthesis of 4-Aryl-2-pyrrolidones and β-Aryl-γ-amino-butyric Acid (GABA) Analogues by Heck Arylation of 3-Pyrrolines with Arenediazonium Tetrafluoroborates. Synthesis of (±)-Rolipram on a Multigram Scale and Chromatographic Resolution by Semipreparative Chiral Simulated Moving Bed Chromatography
inferredcites →https://doi.org/10.1021/jo301506popenalex-snapshot
Regio- and Enantioselective Palladium-Catalyzed Allylic Alkylation of Nitromethane with Monosubstituted Allyl Substrates: Synthesis of (R)-Rolipram and (R)-Baclofen
inferredcites →https://doi.org/10.1021/ol103054aopenalex-snapshot
Asymmetric Synthesis of β-Substituted γ-Lactams via Rhodium/Diene-Catalyzed 1,4-Additions: Application to the Synthesis of (R)-Baclofen and (R)-Rolipram
inferredcites →https://doi.org/10.1021/ol303505kopenalex-snapshot
Copper-Catalyzed Asymmetric Conjugate Addition of Alkenyl- and Alkylalanes to α,β-Unsaturated Lactams
inferredcites →https://doi.org/10.1038/nature14343openalex-snapshot
Multistep continuous-flow synthesis of (R)- and (S)-rolipram using heterogeneous catalysts
inferredcites →https://doi.org/10.1038/nchem.1222openalex-snapshot
Enantioselective construction of quaternary N-heterocycles by palladium-catalysed decarboxylative allylic alkylation of lactams
inferredcites →https://doi.org/10.1038/nm.4011openalex-snapshot
Tau-driven 26S proteasome impairment and cognitive dysfunction can be prevented early in disease by activating cAMP-PKA signaling
inferredcites →https://doi.org/10.1039/b403793fopenalex-snapshot
Unprecedented copper-catalyzed asymmetric conjugate addition of organometallic reagents to α,β-unsaturated lactams
inferredcites →https://doi.org/10.1039/c1sc00724fopenalex-snapshot
Direct aerobic α,β-dehydrogenation of aldehydes and ketones with a Pd(TFA) 2 /4,5-diazafluorenone catalyst
inferredcites →https://doi.org/10.1039/c5sc01636copenalex-snapshot
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
inferredcites →https://doi.org/10.1039/c6ob01349jopenalex-snapshot
Biologically active γ-lactams: synthesis and natural sources
inferredcites →https://doi.org/10.1055/s-0032-1316874openalex-snapshot
From Paracetamol to Rolipram and Derivatives: Application of Deacetylation-Diazotation Sequences and Palladium-Catalyzed Matsuda-Heck Reaction
inferredcites →https://doi.org/10.1080/00397919708004171openalex-snapshot
Synthesis of the Novel Antidepressant (R)-(-)-Rolipram
inferredcites →https://doi.org/10.1246/cl.1976.559openalex-snapshot
NEW CROSS-ALDOL REACTION Via VINYLOXYBORANES

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4530852openalex-extracted
New Synthesis of Β-Aryl-Gaba Drugs
inferred← citeshttps://doi.org/10.1002/0471264229.os098.11openalex-snapshot
Enantioselective Michael‐Proton Transfer‐Lactamization for Pyroglutamic Acid Derivatives: Synthesis of Dimethyl‐( S , E )‐5‐oxo‐3‐styryl‐1‐tosylpyrrolidine‐2,2‐dicarboxylate
inferred← citeshttps://doi.org/10.1002/adsc.201801058openalex-snapshot
Synthesis of Enones and Enals via Dehydrogenation of Saturated Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.201900419openalex-snapshot
Intermolecular Multiple Dehydrogenative Cross‐Couplings of Ketones with Boronic Acids and Amines via Copper Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.202000454openalex-snapshot
Direct Dehydrogenation for the Synthesis of α,β‐Unsaturated Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/ajoc.70261openalex-snapshot
Recent Advances for the Desaturation of Amides
inferred← citeshttps://doi.org/10.1002/ange.201800958openalex-snapshot
Direct Palladium‐Catalyzed β‐Arylation of Lactams
inferred← citeshttps://doi.org/10.1002/ange.201808794openalex-snapshot
Chemoselektive α,β‐Dehydrierung von gesättigten Amiden
inferred← citeshttps://doi.org/10.1002/ange.201811197openalex-snapshot
Platinum‐Catalyzed Desaturation of Lactams, Ketones, and Lactones
inferred← citeshttps://doi.org/10.1002/ange.201907523openalex-snapshot
Enantioselective Total Syntheses of Pallambins A–D
inferred← citeshttps://doi.org/10.1002/ange.201914868openalex-snapshot
Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)‐Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction
inferred← citeshttps://doi.org/10.1002/ange.202008242openalex-snapshot
A Divergent Enantioselective Total Synthesis of Post‐Iboga Indole Alkaloids
inferred← citeshttps://doi.org/10.1002/ange.202013628openalex-snapshot
Platinum‐Catalyzed α,β‐Desaturation of Cyclic Ketones through Direct Metal–Enolate Formation
inferred← citeshttps://doi.org/10.1002/ange.202014900openalex-snapshot
1,2‐Aryl Migration Induced by Amide C−N Bond‐Formation: Reaction of Alkyl Aryl Ketones with Primary Amines Towards α,α‐Diaryl β,γ‐Unsaturated γ‐Lactams
inferred← citeshttps://doi.org/10.1002/ange.202108120openalex-snapshot
Palladium‐Catalyzed Cascade Carbonylation to α,β‐Unsaturated Piperidones via Selective Cleavage of Carbon–Carbon Triple Bonds
inferred← citeshttps://doi.org/10.1002/ange.202402638openalex-snapshot
Accessing Z‐Enynes via Cobalt‐Catalyzed Propargylic Dehydrogenation
inferred← citeshttps://doi.org/10.1002/ange.202514539openalex-snapshot
EDA Complex‐Driven Desaturation of Heterocyclic Carbonyl Compounds Enabled by HFIP
inferred← citeshttps://doi.org/10.1002/anie.201800958openalex-snapshot
Direct Palladium‐Catalyzed β‐Arylation of Lactams
inferred← citeshttps://doi.org/10.1002/anie.201808794openalex-snapshot
Chemoselective α,β‐Dehydrogenation of Saturated Amides
inferred← citeshttps://doi.org/10.1002/anie.201811197openalex-snapshot
Platinum‐Catalyzed Desaturation of Lactams, Ketones, and Lactones
inferred← citeshttps://doi.org/10.1002/anie.201907523openalex-snapshot
Enantioselective Total Syntheses of Pallambins A–D
inferred← citeshttps://doi.org/10.1002/anie.201914868openalex-snapshot
Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)‐Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction
inferred← citeshttps://doi.org/10.1002/anie.202008242openalex-snapshot
A Divergent Enantioselective Total Synthesis of Post‐Iboga Indole Alkaloids
inferred← citeshttps://doi.org/10.1002/anie.202013628openalex-snapshot
Platinum‐Catalyzed α,β‐Desaturation of Cyclic Ketones through Direct Metal–Enolate Formation
inferred← citeshttps://doi.org/10.1002/anie.202014900openalex-snapshot
1,2‐Aryl Migration Induced by Amide C−N Bond‐Formation: Reaction of Alkyl Aryl Ketones with Primary Amines Towards α,α‐Diaryl β,γ‐Unsaturated γ‐Lactams
inferred← citeshttps://doi.org/10.1002/anie.202108120openalex-snapshot
Palladium‐Catalyzed Cascade Carbonylation to α,β‐Unsaturated Piperidones via Selective Cleavage of Carbon–Carbon Triple Bonds
inferred← citeshttps://doi.org/10.1002/anie.202402638openalex-snapshot
Accessing Z‐Enynes via Cobalt‐Catalyzed Propargylic Dehydrogenation
inferred← citeshttps://doi.org/10.1002/anie.202514539openalex-snapshot
EDA Complex‐Driven Desaturation of Heterocyclic Carbonyl Compounds Enabled by HFIP
inferred← citeshttps://doi.org/10.1002/cctc.201902150openalex-snapshot
Recent Development on Cp*Ir(III)‐Catalyzed C−H Bond Functionalization
inferred← citeshttps://doi.org/10.1002/chem.201905262openalex-snapshot
Transition‐Metal‐Free Multiple Functionalization of Piperidines to 4‐Substituted and 3,4‐Disubstituted 2‐Piperidinones
inferred← citeshttps://doi.org/10.1002/cjoc.202100001openalex-snapshot
Protecting‐Group‐Free Total Synthesis of (–)‐Pallambins A—D
inferred← citeshttps://doi.org/10.1002/ejoc.202301267openalex-snapshot
Transition‐Metal‐Catalyzed α,β‐Dehydrogenation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/tcr.202300146openalex-snapshot
Oxidative Dehydrogenation of Alkanes through Homogeneous Base Metal Catalysis
inferred← citeshttps://doi.org/10.1016/bs.aihch.2018.10.004openalex-snapshot
Reactions of 3-pyrrolin-2-ones
inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.065openalex-snapshot
Palladium-catalyzed α,β-dehydrogenation of acyclic ester equivalents promoted by a novel electron deficient phosphinooxazoline ligand
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131641openalex-snapshot
An updated asymmetric total synthesis of (+)-tronocarpine
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133648openalex-snapshot
New synthesis of β-aryl-GABA drugs
inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00787openalex-snapshot
Dehydrogenative Pd and Ni Catalysis for Total Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00685openalex-snapshot
Manganese(I) Catalyzed α-Alkenylation of Amides Using Alcohols with Liberation of Hydrogen and Water
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.3c01027openalex-snapshot
Syntheses of Substituted α,β-Unsaturated δ-Lactams from N-Boc-2,4-dioxopiperidine
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02572openalex-snapshot
Comprehensive Mechanistic Analysis of Palladium- and Nickel-Catalyzed α,β-Dehydrogenation of Carbonyls via Organozinc Intermediates
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02060openalex-snapshot
Chemoselective Dehydrogenation and Hetero-Arylation of Amides via Radical Translocation Enabled by Photoexcited Triplet Ketone Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02676openalex-snapshot
Dehydrogenation of Aromatic Alcohols, Aldehydes, and Ketones Catalyzed by Cu(I) Complexes
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01237openalex-snapshot
Iodine-Catalyzed Carbonyl Desaturation: A One-Pot Synthesis of Flavones
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03117openalex-snapshot
Synthetic Strategy: Palladium-Catalyzed Dehydrogenation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00872openalex-snapshot
Radical α,β-Dehydrogenation of Saturated Amides via α-Oxidation with TEMPO under Transition Metal-Free Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02594openalex-snapshot
Photoinduced Desaturation of Amides by Palladium Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01240openalex-snapshot
Iron-Catalyzed Aerobic α,β-Dehydrogenation
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01052openalex-snapshot
Synthesis of Dienamides via Palladium-catalyzed Oxidative N-α,β-Dehydrogenation of Amides
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01067openalex-snapshot
Copper-Catalyzed Dehydrogenative Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04337openalex-snapshot
Total Synthesis of Galanthamine and Lycoramine Featuring an Early-Stage C–C and a Late-Stage Dehydrogenation via C–H Activation
inferred← citeshttps://doi.org/10.1021/acscatal.0c01519openalex-snapshot
Catalytic β-Functionalization of Carbonyl Compounds Enabled by α,β-Desaturation
inferred← citeshttps://doi.org/10.1021/acscatal.0c04712openalex-snapshot
Carbonyl Desaturation: Where Does Catalysis Stand?
inferred← citeshttps://doi.org/10.1021/acscatal.8b00923openalex-snapshot
Rh/Cu-Catalyzed Ketone β-Functionalization by Merging Ketone Dehydrogenation and Carboxyl-Directed C–H Alkylation
inferred← citeshttps://doi.org/10.1021/jacs.0c02654openalex-snapshot
Intramolecular β-Alkenylation of Cyclohexanones via Pd-Catalyzed Desaturation-Mediated C(sp3)–H/Alkyne Coupling
inferred← citeshttps://doi.org/10.1021/jacs.1c05479openalex-snapshot
Site-Selective Acceptorless Dehydrogenation of Aliphatics Enabled by Organophotoredox/Cobalt Dual Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.3c06423openalex-snapshot
Synthesis of β,γ-Unsaturated Aliphatic Acids via Ligand-Enabled Dehydrogenation
inferred← citeshttps://doi.org/10.1021/jacs.3c13085openalex-snapshot
RETRACTED: Hydrogen Atom Transfer (HAT)-Mediated Remote Desaturation Enabled by Fe/Cr–H Cooperative Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.3c13864openalex-snapshot
Asymmetric Synthesis of Nidulalin A and Nidulaxanthone A: Selective Carbonyl Desaturation Using an Oxoammonium Salt
inferred← citeshttps://doi.org/10.1021/jacs.4c07115openalex-snapshot
Iridium-Catalyzed Oxidant-Free Transfer Dehydrogenation of Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/jacs.6c05474openalex-snapshot
Asymmetric Radical Allylic Cyanation of Electron-Deficient Alkenes with a Low Copper Catalyst Loading: Development and Mechanism
inferred← citeshttps://doi.org/10.1021/jacs.6c11696openalex-snapshot
From Dehydrogenation to Derivatization: Functionalization of Alkanes and Alkyl Groups by Molecular Catalysis
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/jacs.7b08813openalex-snapshot
Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides
inferred← citeshttps://doi.org/10.1021/jacs.7b11351openalex-snapshot
Iridium-Catalyzed Aerobic α,β-Dehydrogenation of γ,δ-Unsaturated Amides and Acids: Activation of Both α- and β-C–H bonds through an Allyl–Iridium Intermediate
inferred← citeshttps://doi.org/10.1021/jacs.8b00488openalex-snapshot
General, Mild, and Selective Method for Desaturation of Aliphatic Amines
inferred← citeshttps://doi.org/10.1021/jacs.8b02752openalex-snapshot
Palladium-Catalyzed Enantioselective Relay Heck Arylation of Enelactams: Accessing α,β-Unsaturated δ-Lactams
inferred← citeshttps://doi.org/10.1021/jacs.8b03530openalex-snapshot
Direct β-Alkylation of Ketones and Aldehydes via Pd-Catalyzed Redox Cascade
inferred← citeshttps://doi.org/10.1021/jacs.9b02552openalex-snapshot
Allyl-Nickel Catalysis Enables Carbonyl Dehydrogenation and Oxidative Cycloalkenylation of Ketones
inferred← citeshttps://doi.org/10.1021/jacs.9b07932openalex-snapshot
Copper-Catalyzed Desaturation of Lactones, Lactams, and Ketones under pH-Neutral Conditions
inferred← citeshttps://doi.org/10.1021/jacsau.5c01078openalex-snapshot
Site-Selective Benzylic Dehydrogenation of Alkylindoles
inferred← citeshttps://doi.org/10.1038/s41467-017-02381-8openalex-snapshot
Dehydrogenative desaturation-relay via formation of multicenter-stabilized radical intermediates
inferred← citeshttps://doi.org/10.1038/s41467-018-07534-xopenalex-snapshot
Differentiation between enamines and tautomerizable imines in the oxidation reaction with TEMPO
inferred← citeshttps://doi.org/10.1038/s41467-019-11624-9openalex-snapshot
Copper-catalyzed dehydrogenative γ-C(sp3)-H amination of saturated ketones for synthesis of polysubstituted anilines
inferred← citeshttps://doi.org/10.1038/s41467-024-48737-9openalex-snapshot
A facile synthesis of α,β-unsaturated imines via palladium-catalyzed dehydrogenation
inferred← citeshttps://doi.org/10.1038/s41467-024-49359-xopenalex-snapshot
Tandem dehydrogenation-olefination-decarboxylation of cycloalkyl carboxylic acids via multifold C–H activation
inferred← citeshttps://doi.org/10.1038/s41557-021-00640-2openalex-snapshot
Electrochemically driven desaturation of carbonyl compounds
inferred← citeshttps://doi.org/10.1039/c9sc05970aopenalex-snapshot
A borane-mediated palladium-catalyzed reductive allylic alkylation of α,β-unsaturated carbonyl compounds
inferred← citeshttps://doi.org/10.1039/d0dt04311gopenalex-snapshot
Unexpected binuclear O–O cleavage and radical C–H activation mechanism for Cu-catalyzed desaturation of lactone
inferred← citeshttps://doi.org/10.1039/d2sc02210aopenalex-snapshot
Selective desaturation of amides: a direct approach to enamides
inferred← citeshttps://doi.org/10.1039/d2sc02291eopenalex-snapshot
Cobalt-catalyzed chemoselective dehydrogenation through radical translocation under visible light
inferred← citeshttps://doi.org/10.1039/d2sc05370eopenalex-snapshot
Multiple remote C(sp 3 )–H functionalizations of aliphatic ketones via bimetallic Cu–Pd catalyzed successive dehydrogenation
inferred← citeshttps://doi.org/10.1039/d3cc01960hopenalex-snapshot
Direct synthesis of alkylated 4-hydroxycoumarin derivatives via a cascade Cu-catalyzed dehydrogenation/conjugate addition sequence
inferred← citeshttps://doi.org/10.1039/d3cc05191aopenalex-snapshot
Pd( ii )-Catalyzed tandem selective dehydrogenative [4+2] annulation of 2-methyl-1,3-cycloalkanediones with olefins
inferred← citeshttps://doi.org/10.1039/d3qo02045bopenalex-snapshot
Straightforward α-allylation of carbonyl compounds with alkenes via α-carbonyl radical intermediates
inferred← citeshttps://doi.org/10.1039/d4cc02609hopenalex-snapshot
Versatile dehydrogenation of carbonyls enabled by an iodine( iii ) reagent
inferred← citeshttps://doi.org/10.1039/d4sc04419copenalex-snapshot
Catalytic dehydrogenative synthesis of α,β-unsaturated secondary amides without external oxidants
inferred← citeshttps://doi.org/10.1039/d6ob00514dopenalex-snapshot
Base-promoted synthesis of α,β-unsaturated amides via C–N bond formation using α,β-unsaturated acids and isothiocyanates
inferred← citeshttps://doi.org/10.1055/a-2288-6944openalex-snapshot
A Photochemical Strategy for the Synthesis of Caprolactams via Dearomative Ring Expansion of Nitroarenes
inferred← citeshttps://doi.org/10.1055/sos-sd-147-00010openalex-snapshot
47.1.4.11 Synthesis of Alkenes by α,β-Dehydrogenation
inferred← citeshttps://doi.org/10.1126/science.abl3939openalex-snapshot
Ligand-controlled divergent dehydrogenative reactions of carboxylic acids via C–H activation
inferred← citeshttps://doi.org/10.15227/orgsyn.098.0194openalex-snapshot
Enantioselective Michael-Proton Transfer-Lactamization for Pyroglutamic Acid Derivatives: Synthesis of Dimethyl-(S,E)-5-oxo-3-styryl-1-tosylpyrrolidine-2,2-dicarboxylate
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3260796/v1openalex-snapshot
Hydrogen Atom Transfer (HAT)-Mediated Remote Desaturation Enabled by Fe/Cr-H Cooperative Catalysis
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-0t55gopenalex-snapshot
A Comparative Mechanistic Analysis of Palladium- and Nickel-Catalyzed α,β-Dehydrogenation of Carbonyls via Organozinc Intermediates
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-0t55g-v2openalex-snapshot
A Comprehensive Mechanistic Analysis of Palladium- and Nickel-Catalyzed α,β-Dehydrogenation of Carbonyls via Organozinc Intermediates
inferred← citeshttps://doi.org/10.5757/asct.2022.31.3.63openalex-snapshot
Recent Advances in the Low-Temperature Chemical Vapor Deposition Growth of Graphene
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.