On the public citation graph

Three-component reductive conjugate addition/aldol tandem reaction enabled by nickel/photoredox dual catalysis

https://doi.org/10.1039/d2sc06303d
0 signed · 84 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/anie.200500195openalex-snapshot
Catalytic Asymmetric Tandem Transformations Triggered by Conjugate Additions
inferredcites →https://doi.org/10.1002/anie.201606458openalex-snapshot
Tandem Difluoroalkylation‐Arylation of Enamides Catalyzed by Nickel
inferredcites →https://doi.org/10.1002/anie.201900228openalex-snapshot
Nickel‐Catalyzed Asymmetric Reductive Diarylation of Vinylarenes
inferredcites →https://doi.org/10.1002/anie.201908029openalex-snapshot
Enantioselective Radical Addition/Cross‐Coupling of Organozinc Reagents, Alkyl Iodides, and Alkenyl Boron Reagents
inferredcites →https://doi.org/10.1002/anie.201914175openalex-snapshot
Nickel/Photoredox‐Catalyzed Asymmetric Reductive Cross‐Coupling of Racemic α‐Chloro Esters with Aryl Iodides
inferredcites →https://doi.org/10.1002/anie.201916279openalex-snapshot
Site‐Selective 1,2‐Dicarbofunctionalization of Vinyl Boronates through Dual Catalysis
inferredcites →https://doi.org/10.1002/anie.202006439openalex-snapshot
Selective 1,2‐Aryl‐Aminoalkylation of Alkenes Enabled by Metallaphotoredox Catalysis
inferredcites →https://doi.org/10.1002/anie.202114731openalex-snapshot
From Esters to Ketones via a Photoredox‐Assisted Reductive Acyl Cross‐Coupling Strategy
inferredcites →https://doi.org/10.1002/chem.200500622openalex-snapshot
Cyclic Enolates of Ni and Pd: Equilibrium between C‐ and O‐Bound Tautomers and Reactivity Studies
inferredcites →https://doi.org/10.1002/chem.201604251openalex-snapshot
Cobalt‐Catalyzed Reductive Multicomponent Synthesis of β‐Hydroxy‐ and β‐Aminocarbonyl Compounds under Mild Conditions
inferredcites →https://doi.org/10.1002/tcr.201700098openalex-snapshot
Transition Metal‐Catalyzed Dicarbofunctionalization of Unactivated Olefins
inferredcites →https://doi.org/10.1016/0009-2614(86)80542-5openalex-snapshot
Oxidation potentials of α-aminoalkyl radicals: bond dissociation energies for related radical cations
inferredcites →https://doi.org/10.1016/j.chempr.2019.12.026openalex-snapshot
Broadly Applicable Directed Catalytic Reductive Difunctionalization of Alkenyl Carbonyl Compounds
inferredcites →https://doi.org/10.1021/acs.accounts.5b00057openalex-snapshot
Methods and Mechanisms for Cross-Electrophile Coupling of Csp2 Halides with Alkyl Electrophiles
inferredcites →https://doi.org/10.1021/acs.accounts.6b00214openalex-snapshot
Single-Electron Transmetalation via Photoredox/Nickel Dual Catalysis: Unlocking a New Paradigm for sp3–sp2 Cross-Coupling
inferredcites →https://doi.org/10.1021/acs.accounts.6b00251openalex-snapshot
Synthetic Utilization of α-Aminoalkyl Radicals and Related Species in Visible Light Photoredox Catalysis
inferredcites →https://doi.org/10.1021/acs.chemrev.1c00383openalex-snapshot
Metallaphotoredox: The Merger of Photoredox and Transition Metal Catalysis
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00018openalex-snapshot
Dual Catalysis Strategies in Photochemical Synthesis
inferredcites →https://doi.org/10.1021/acs.orglett.2c01237openalex-snapshot
Nickel-Catalyzed Three-Component Alkylacylation of Alkenes Enabled by a Photoactive Electron Donor–Acceptor Complex
inferredcites →https://doi.org/10.1021/acs.orglett.2c01416openalex-snapshot
Ni-Catalyzed Reductive 1,2-Cross-Dialkylation of Unactivated Alkenes with Two Alkyl Bromides
inferredcites →https://doi.org/10.1021/acs.orglett.6b01837openalex-snapshot
Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Alkyl Bromides: Et3N as the Terminal Reductant
inferredcites →https://doi.org/10.1021/acs.orglett.9b01097openalex-snapshot
Deaminative Reductive Arylation Enabled by Nickel/Photoredox Dual Catalysis
inferredcites →https://doi.org/10.1021/acscatal.0c01199openalex-snapshot
Regioselective Cross-Electrophile Coupling of Epoxides and (Hetero)aryl Iodides via Ni/Ti/Photoredox Catalysis
inferredcites →https://doi.org/10.1021/acscatal.0c02115openalex-snapshot
Nickel-Catalyzed Dicarbofunctionalization of Alkenes
inferredcites →https://doi.org/10.1021/acscatal.2c03805openalex-snapshot
The Merger of Benzophenone HAT Photocatalysis and Silyl Radical-Induced XAT Enables Both Nickel-Catalyzed Cross-Electrophile Coupling and 1,2-Dicarbofunctionalization of Olefins
inferredcites →https://doi.org/10.1021/acscatal.7b01973openalex-snapshot
Aminomethylation of Aryl Halides Using α-Silylamines Enabled by Ni/Photoredox Dual Catalysis
inferredcites →https://doi.org/10.1021/cr300503ropenalex-snapshot
Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
inferredcites →https://doi.org/10.1021/ja00161a049openalex-snapshot
Electrochemical oxidation of organosilicon compounds. Part 7. The origin of .beta.-silicon effect in electron-transfer reactions of silicon-substituted heteroatom compounds. Electrochemical and theoretical studies
inferredcites →https://doi.org/10.1021/ja01565a041openalex-snapshot
The Stereochemistry of the Ivanov and Reformatsky Reactions. I
inferredcites →https://doi.org/10.1021/ja0362048openalex-snapshot
A New Catalytic Conjugate Addition/Aldol Strategy That Avoids Preformed Metalated Nucleophiles
inferredcites →https://doi.org/10.1021/jacs.0c03708openalex-snapshot
Enantioselective Three-Component Fluoroalkylarylation of Unactivated Olefins through Nickel-Catalyzed Cross-Electrophile Coupling
inferredcites →https://doi.org/10.1021/jacs.0c09922openalex-snapshot
Chemoselective Union of Olefins, Organohalides, and Redox-Active Esters Enables Regioselective Alkene Dialkylation
inferredcites →https://doi.org/10.1021/jacs.2c06636openalex-snapshot
Three-Component Asymmetric Ni-Catalyzed 1,2-Dicarbofunctionalization of Unactivated Alkenes via Stereoselective Migratory Insertion
inferredcites →https://doi.org/10.1021/jacs.2c08039openalex-snapshot
Remote and Proximal Hydroaminoalkylation of Alkenes Enabled by Photoredox/Nickel Dual Catalysis
inferredcites →https://doi.org/10.1021/jacs.6b04818openalex-snapshot
Silyl Radical Activation of Alkyl Halides in Metallaphotoredox Catalysis: A Unique Pathway for Cross-Electrophile Coupling
inferredcites →https://doi.org/10.1021/jacs.7b03195openalex-snapshot
Nickel-Catalyzed Reductive Dicarbofunctionalization of Alkenes
inferredcites →https://doi.org/10.1021/jacs.7b06340openalex-snapshot
Ni-Catalyzed Regioselective 1,2-Dicarbofunctionalization of Olefins by Intercepting Heck Intermediates as Imine-Stabilized Transient Metallacycles
inferredcites →https://doi.org/10.1021/jacs.7b06567openalex-snapshot
Nickel-Catalyzed β,γ-Dicarbofunctionalization of Alkenyl Carbonyl Compounds via Conjunctive Cross-Coupling
inferredcites →https://doi.org/10.1021/jacs.8b05680openalex-snapshot
Nickel-Catalyzed Stereoselective Diarylation of Alkenylarenes
inferredcites →https://doi.org/10.1021/jacs.9b02973openalex-snapshot
Ni-Catalyzed Reductive Dicarbofunctionalization of Nonactivated Alkenes: Scope and Mechanistic Insights
inferredcites →https://doi.org/10.1021/om00115a007openalex-snapshot
Synthesis and reactions of nickel and palladium carbon-bound enolate complexes
inferredcites →https://doi.org/10.1038/s41467-021-26794-8openalex-snapshot
Catalytic enantioselective reductive domino alkyl arylation of acrylates via nickel/photoredox catalysis
inferredcites →https://doi.org/10.1038/s41557-021-00836-6openalex-snapshot
Directing-group-free catalytic dicarbofunctionalization of unactivated alkenes
inferredcites →https://doi.org/10.1038/s41929-022-00854-8openalex-snapshot
Synthesis of tri- and tetrasubstituted stereocentres by nickel-catalysed enantioselective olefin cross-couplings
inferredcites →https://doi.org/10.1039/b816853aopenalex-snapshot
Recent advances in enantioselective copper-catalyzed 1,4-addition
inferredcites →https://doi.org/10.1039/c5qo00224aopenalex-snapshot
Nickel-catalyzed reductive coupling of alkyl halides with other electrophiles: concept and mechanistic considerations
inferredcites →https://doi.org/10.1039/c7sc03149aopenalex-snapshot
Nickel-catalyzed difunctionalization of allyl moieties using organoboronic acids and halides with divergent regioselectivities
inferredcites →https://doi.org/10.1039/c9sc06006eopenalex-snapshot
Recent developments in nickel-catalyzed intermolecular dicarbofunctionalization of alkenes
inferredcites →https://doi.org/10.1039/d0sc02054kopenalex-snapshot
Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates
inferredcites →https://doi.org/10.1039/d1cs00399bopenalex-snapshot
Catalytic three-component dicarbofunctionalization reactions involving radical capture by nickel
inferredcites →https://doi.org/10.1126/science.1255525openalex-snapshot
Merging photoredox with nickel catalysis: Coupling of α-carboxyl sp 3 -carbons with aryl halides
inferredcites →https://doi.org/10.1126/science.aaf6123openalex-snapshot
A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents

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.4662834openalex-extracted
Photoredox/Nickel Dual-Catalysis-Enabled Regioselective Cyclization of Alkenes with Alkyl Chlorides
inferred← citeshttps://doi.org/10.1002/adsc.70192openalex-snapshot
Nickel/Photoredox‐Catalyzed Reductive Aldol Reaction
inferred← citeshttps://doi.org/10.1002/ange.202314304openalex-snapshot
Construction of Bridged Benzazepines via Photo‐Induced Dearomatization
inferred← citeshttps://doi.org/10.1002/anie.202314304openalex-snapshot
Construction of Bridged Benzazepines via Photo‐Induced Dearomatization
inferred← citeshttps://doi.org/10.1002/cctc.202500106openalex-snapshot
Photoredox/Nickel‐Catalyzed Cross‐Coupling of Alkynyl Bromides and α‐Silylamines for the Synthesis of Propynylamines
inferred← citeshttps://doi.org/10.1002/chem.202402712openalex-snapshot
Visible‐Light Mediated Nickel‐Catalyzed Asymmetric Difunctionalizations of Alkenes
inferred← citeshttps://doi.org/10.1007/s11172-024-4191-0openalex-snapshot
α-Silyl amines as electron donors: application in synthetic organic chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00021-1openalex-snapshot
Reductive Dicarbofunctionalization of C–C π-Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00037-5openalex-snapshot
Reductive Metal-Catalyzed Coupling as an Alternative to the Use of Stoichiometric Organometallic Reagents in Carbonyl and Imine Additions
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00068-5openalex-snapshot
The Aldol Reaction: Transition Metal Enolates
inferred← citeshttps://doi.org/10.1016/j.checat.2023.100819openalex-snapshot
Ni-catalyzed reductive alkylgermylation of activated alkenes: Modular access to polyfunctionalized alkyl germanes
inferred← citeshttps://doi.org/10.1016/j.mcat.2023.113806openalex-snapshot
Photoredox/nickel dual-catalysis-enabled synthesis of N-heterocycles from alkyl chlorides and alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01483openalex-snapshot
Visible-Light-Mediated Three-Component Decarboxylative Coupling Reactions to Synthesize 1,4-Diol Monoethers
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00375openalex-snapshot
Cu(II)-Catalyzed Three-Component Sila-Strecker Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00763openalex-snapshot
TMSOTf-Catalyzed [4 + 2] Annulation of Ynamides and β-(2-Aminophenyl)-α,β-ynones for the Synthesis 2-Aminoquinolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03151openalex-snapshot
Nickel/Photoredox-Catalyzed Asymmetric Three-Component Cross-Coupling To Access Enantioenriched 1,1-Diaryl(heteroaryl)alkanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03391openalex-snapshot
Nickel/Photoredox-Catalyzed Reductive Alkylation/Aldol Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00677openalex-snapshot
Photoredox/Nickel-Catalyzed Hydrogenation of Alkenes Using Water as the Hydrogen Source
inferred← citeshttps://doi.org/10.1021/acscatal.4c01312openalex-snapshot
Ligand-Controlled Regioreversed 1,2-Aryl-Aminoalkylation of Alkenes Enabled by Photoredox/Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acscentsci.6c01081openalex-snapshot
Adamantyl-BOX Ligand Enabling Stereoselective Synthesis of Axially Chiral Aldehydes Bearing Vicinal Stereogenic Centers
inferred← citeshttps://doi.org/10.1021/jacs.3c09705openalex-snapshot
Nickel/Photoredox Dual-Catalyzed Regiodivergent Aminoalkylation of Unactivated Alkyl Halides
inferred← citeshttps://doi.org/10.1039/d3qo01927fopenalex-snapshot
Nickel/photoredox dual-catalyzed reductive cross-coupling of aryl halides and aldehydes
inferred← citeshttps://doi.org/10.1039/d4cc02914copenalex-snapshot
Recent advances in dual photoredox/nickel catalyzed alkene carbofunctionalised reactions
inferred← citeshttps://doi.org/10.1039/d4sc07728hopenalex-snapshot
Ni-catalyzed regioselective and site-divergent reductive arylalkylations of allylic amines
inferred← citeshttps://doi.org/10.1039/d5cc04974aopenalex-snapshot
Photoredox-catalyzed nucleophilic addition of α-amino radicals to unsaturated compounds
inferred← citeshttps://doi.org/10.1039/d5cs00670hopenalex-snapshot
Intermolecular 1,2-difunctionalization of alkenes
inferred← citeshttps://doi.org/10.1039/d5np00030kopenalex-snapshot
Photo-/electro-chemical catalysis: a promising toolkit for late-stage functionalization of alkene-containing natural products
inferred← citeshttps://doi.org/10.1039/d6sc00822dopenalex-snapshot
On-complex three-component cascade reactions involving phosphorescent cyclometalated Ir( iii ) chloro-isocyanide complexes, nitriles, and propylamine
inferred← citeshttps://doi.org/10.1055/a-2577-4281openalex-snapshot
Nickel/Photoredox-Catalyzed Three-Component Dialkylation of Alkenes for the Synthesis of β-Amino Acid Derivatives
inferred← citeshttps://doi.org/10.20517/cs.2024.140openalex-snapshot
Three-component cross-coupling reactions involving alkenes enabled by visible-light and earth-abundant-metal-catalysis
inferred← citeshttps://doi.org/10.20517/cs.2024.89openalex-snapshot
Photoredox/nickel dual-catalyzed reductive C(sp 2 )–Si cross-coupling
inferred← citeshttps://doi.org/10.6023/cjoc202408039openalex-snapshot
Photoinduced Nickel-Catalyzed Reductive Heck Reaction
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.