On the public citation graph

Expedient Access to Underexplored Chemical Space: Deoxygenative C(sp 3 )–C(sp 3 ) Cross-Coupling

https://doi.org/10.1021/jacs.3c01488
0 signed · 145 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/(sici)1521-3773(19980918)37:17<2387::aid-anie2387>3.0.co;2-mopenalex-snapshot
An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers
inferredcites →https://doi.org/10.1002/anie.201107017openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize
inferredcites →https://doi.org/10.1002/anie.202207150openalex-snapshot
Alcohols as Alkylating Agents: Photoredox‐Catalyzed Conjugate Alkylation via In Situ Deoxygenation
inferredcites →https://doi.org/10.1002/chem.201405223openalex-snapshot
Copper‐Catalyzed Reductive Cross‐Coupling of Nonactivated Alkyl Tosylates and Mesylates with Alkyl and Aryl Bromides
inferredcites →https://doi.org/10.1002/chem.201500110openalex-snapshot
Computational Insight into Nickel‐Catalyzed Carbon–Carbon versus Carbon–Boron Coupling Reactions of Primary, Secondary, and Tertiary Alkyl Bromides
inferredcites →https://doi.org/10.1016/j.bmc.2018.02.032openalex-snapshot
Design, synthesis and biological evaluation of novel 7-azaspiro[3.5]nonane derivatives as GPR119 agonists
inferredcites →https://doi.org/10.1016/j.ijpharm.2009.01.026openalex-snapshot
An interesting relationship between drug absorption and melting point
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.jmedchem.2c00473openalex-snapshot
Rings in Clinical Trials and Drugs: Present and Future
inferredcites →https://doi.org/10.1021/acs.jnatprod.8b01022openalex-snapshot
A Systematic Cheminformatics Analysis of Functional Groups Occurring in Natural Products
inferredcites →https://doi.org/10.1021/acs.organomet.2c00032openalex-snapshot
Recent Advances in C(sp3)–C(sp3) Cross-Coupling Chemistry: A Dominant Performance of Nickel Catalysts
inferredcites →https://doi.org/10.1021/acscatal.9b03352openalex-snapshot
Nickel/Cobalt-Catalyzed C(sp 3 )–C(sp 3 ) Cross-Coupling of Alkyl Halides with Alkyl Tosylates
inferredcites →https://doi.org/10.1021/cm051312+openalex-snapshot
Single-Layer Electroluminescent Devices and Photoinduced Hydrogen Production from an Ionic Iridium(III) Complex
inferredcites →https://doi.org/10.1021/cr0505268openalex-snapshot
Selected Patented Cross-Coupling Reaction Technologies
inferredcites →https://doi.org/10.1021/ed1003806openalex-snapshot
A Graphical Journey of Innovative Organic Architectures That Have Improved Our Lives
inferredcites →https://doi.org/10.1021/ja0345221openalex-snapshot
Efficient Yellow Electroluminescence from a Single Layer of a Cyclometalated Iridium Complex
inferredcites →https://doi.org/10.1021/ja0389366openalex-snapshot
Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides
inferredcites →https://doi.org/10.1021/ja4034999openalex-snapshot
Functional-Group-Tolerant, Nickel-Catalyzed Cross-Coupling Reaction for Enantioselective Construction of Tertiary Methyl-Bearing Stereocenters
inferredcites →https://doi.org/10.1021/ja513079ropenalex-snapshot
Nickel-Catalyzed Cross-Coupling of Photoredox-Generated Radicals: Uncovering a General Manifold for Stereoconvergence in Nickel-Catalyzed Cross-Couplings
inferredcites →https://doi.org/10.1021/jacs.2c02062openalex-snapshot
Nontraditional Fragment Couplings of Alcohols and Carboxylic Acids: C( sp 3 )–C( sp 3 ) Cross-Coupling via Radical Sorting
inferredcites →https://doi.org/10.1021/jacs.2c04807openalex-snapshot
Deoxytrifluoromethylation of Alcohols
inferredcites →https://doi.org/10.1021/jm901241eopenalex-snapshot
Escape from Flatland: Increasing Saturation as an Approach to Improving Clinical Success
inferredcites →https://doi.org/10.1021/jm9602928openalex-snapshot
The Properties of Known Drugs. 1. Molecular Frameworks
inferredcites →https://doi.org/10.1021/ol300891kopenalex-snapshot
Traceless Directing Group for Stereospecific Nickel-Catalyzed Alkyl−Alkyl Cross-Coupling Reactions
inferredcites →https://doi.org/10.1038/nature19056openalex-snapshot
Metallaphotoredox-catalysed sp3–sp3 cross-coupling of carboxylic acids with alkyl halides
inferredcites →https://doi.org/10.1038/s41586-021-03920-6openalex-snapshot
Metallaphotoredox-enabled deoxygenative arylation of alcohols
inferredcites →https://doi.org/10.1039/c2md20347bopenalex-snapshot
Escape from Flatland 2: complexity and promiscuity
inferredcites →https://doi.org/10.1080/14786445008646627openalex-snapshot
XLV. Theory of ætherification
inferredcites →https://doi.org/10.1126/science.1213920openalex-snapshot
Discovery of an α-Amino C–H Arylation Reaction Using the Strategy of Accelerated Serendipity
inferredcites →https://doi.org/10.1126/science.aaf7230openalex-snapshot
Transition metal–catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry

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.202400899openalex-snapshot
Recyclable All‐in‐One Organo‐Photo‐Auxiliaries Enabling (sp3)C−(sp3)C Coupling Reactions with Diverse Functionalities
inferred← citeshttps://doi.org/10.1002/adsc.70207openalex-snapshot
Catalytic Photoactive Ternary Electron Donor–Acceptor Complex Enabled Synthesis of Isoquinoline‐1,3(2H,4H)‐Diones
inferred← citeshttps://doi.org/10.1002/adsc.70524openalex-snapshot
C‐/N‐Glycoside Synthesis Enabled by Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1002/advs.202411788openalex-snapshot
Organophotocatalyst Enabled Deoxycyclopropanation of Alcohols
inferred← citeshttps://doi.org/10.1002/ajoc.202300275openalex-snapshot
Recent Advances in Carbonyl‐Photoredox/Transition Metal Dual Catalysis
inferred← citeshttps://doi.org/10.1002/ajoc.202500568openalex-snapshot
Deoxygenation of Alcohols in Organic Electrosynthesis: Basic Strategies and Recent Developments
inferred← citeshttps://doi.org/10.1002/ange.202401451openalex-snapshot
Diversified Synthesis of Chiral Fluorinated Cyclobutane Derivatives Enabled by Regio‐ and Enantioselective Hydroboration
inferred← citeshttps://doi.org/10.1002/ange.202403119openalex-snapshot
Cross‐selective Deoxygenative Coupling of Aliphatic Alcohols: Installation of Methyl Groups including Isotopic Labels by Nickel Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202405449openalex-snapshot
Photoinduced Low‐Valent Zirconium Catalysis for Cross‐Electrophile Coupling of Ethers
inferred← citeshttps://doi.org/10.1002/ange.202415164openalex-snapshot
Access to Alkenyl Cyclobutanols by Ni‐Catalyzed Regio‐ and Enantio‐Selective syn ‐Hydrometalative 4‐ exo ‐ trig Cyclization of Alkynones
inferred← citeshttps://doi.org/10.1002/ange.202421256openalex-snapshot
Heterocoupling Two Similar Benzyl Radicals by Dual Photoredox/Cobalt Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202423795openalex-snapshot
Alcohol Activation by Benzodithiolylium for Deoxygenative Alkylation Driven by Photocatalytic Energy Transfer
inferred← citeshttps://doi.org/10.1002/ange.202509657openalex-snapshot
Nickel‐Catalyzed Suzuki–Miyaura Cross‐Coupling Reaction of Aliphatic Alcohol Derivatives
inferred← citeshttps://doi.org/10.1002/ange.202516173openalex-snapshot
Nickel‐Catalyzed O ‐Alkylisourea‐Enabled Electrochemical Radical C(sp 3 )−C(sp 2 ) Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/ange.202517652openalex-snapshot
Ligand‐Enabled Cu‐Catalyzed Deoxyalkynylation of α‐Unfunctionalized Alcohols with Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/anie.202401451openalex-snapshot
Diversified Synthesis of Chiral Fluorinated Cyclobutane Derivatives Enabled by Regio‐ and Enantioselective Hydroboration
inferred← citeshttps://doi.org/10.1002/anie.202403119openalex-snapshot
Cross‐selective Deoxygenative Coupling of Aliphatic Alcohols: Installation of Methyl Groups including Isotopic Labels by Nickel Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202405449openalex-snapshot
Photoinduced Low‐Valent Zirconium Catalysis for Cross‐Electrophile Coupling of Ethers
inferred← citeshttps://doi.org/10.1002/anie.202415164openalex-snapshot
Access to Alkenyl Cyclobutanols by Ni‐Catalyzed Regio‐ and Enantio‐Selective syn ‐Hydrometalative 4‐ exo ‐ trig Cyclization of Alkynones
inferred← citeshttps://doi.org/10.1002/anie.202421256openalex-snapshot
Heterocoupling Two Similar Benzyl Radicals by Dual Photoredox/Cobalt Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202423795openalex-snapshot
Alcohol Activation by Benzodithiolylium for Deoxygenative Alkylation Driven by Photocatalytic Energy Transfer
inferred← citeshttps://doi.org/10.1002/anie.202509657openalex-snapshot
Nickel‐Catalyzed Suzuki–Miyaura Cross‐Coupling Reaction of Aliphatic Alcohol Derivatives
inferred← citeshttps://doi.org/10.1002/anie.202516173openalex-snapshot
Nickel‐Catalyzed O ‐Alkylisourea‐Enabled Electrochemical Radical C(sp 3 )−C(sp 2 ) Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/anie.202517652openalex-snapshot
Ligand‐Enabled Cu‐Catalyzed Deoxyalkynylation of α‐Unfunctionalized Alcohols with Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/asia.70768openalex-snapshot
SO 2 ‐Mediated Decarboxylative C(sp 3 )–C(sp 3 ) Coupling of Carboxylic Acids Enabled by Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202303537openalex-snapshot
Blue‐Light Irradiated Mn(0)‐Catalyzed Hydroxylation and C(sp3)−H Functionalization of Unactivated Alkanes with C(sp2)−H Bonds of Quinones for Alkylated Hydroxy Quinones and Parvaquone
inferred← citeshttps://doi.org/10.1002/chem.71191openalex-snapshot
Nickel‐Catalyzed Radical‐Radical Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.202300832openalex-snapshot
Radical Acylation of Alkenes by NHC‐Organocatalysis
inferred← citeshttps://doi.org/10.1002/ejoc.202400845openalex-snapshot
Oxidative Cleavage of Alkoxyamines for Nucleophilic Substitution Reactions
inferred← citeshttps://doi.org/10.1002/ijch.70017openalex-snapshot
Carbohydrate‐Based Drug Discovery: Synthetic Strategies and Clinical Applications
inferred← citeshttps://doi.org/10.1002/tcr.202400161openalex-snapshot
Organometallic Photocatalyst‐Promoted Synthesis and Modification of Carbohydrates under Photoirradiation
inferred← citeshttps://doi.org/10.1007/s11426-025-2651-2openalex-snapshot
Deoxygenative radical reactions of alcohols: a review
inferred← citeshttps://doi.org/10.1007/s11426-025-2666-yopenalex-snapshot
Enantioconvergent deoxygenative reductive cross-coupling of lactic acid derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00030-2openalex-snapshot
Coupling Reaction Between sp3-Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00155-1openalex-snapshot
Photoredox Catalysis
inferred← citeshttps://doi.org/10.1016/bs.aihch.2024.04.004openalex-snapshot
Recent advances in the synthesis of 3,3-disubstituted oxetanes
inferred← citeshttps://doi.org/10.1016/j.checat.2024.101187openalex-snapshot
Deoxygenative alcohol-nucleophile coupling via carbocations
inferred← citeshttps://doi.org/10.1016/j.chempr.2026.103249openalex-snapshot
Carbometallation with alcohols: A facile strategy for olefin synthesis via deoxygenative hydroalkylation
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/10.1016/j.scp.2024.101855openalex-snapshot
Synthesis and modification of carbohydrates using metallaphotoredox catalysis and photoexcited-state transition metal catalysis
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134805openalex-snapshot
Engaging aliphatic mesylates in Suzuki-Miyaura cross-coupling for late-stage functionalization
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155838openalex-snapshot
A reaction enumeration analysis of building blocks to target novel coupling methods
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c02109openalex-snapshot
Photochemistry in Medicinal Chemistry and Chemical Biology
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02351openalex-snapshot
At the Speed of Light: The Systematic Implementation of Photoredox Cross-Coupling Reactions for Medicinal Chemistry Research
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02740openalex-snapshot
Revealing the Mechanism of Alcohol Dehydroxylation and C–C Bond Formation through Concerted Catalysis by Ir/Cu Bimetallic Complexes
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00799openalex-snapshot
Stereoselective Synthesis of Baloxavir Marboxil Using Diastereoselective Cyclization and Photoredox Decarboxylation of l -Serine
inferred← citeshttps://doi.org/10.1021/acs.joc.5c03286openalex-snapshot
Deoxygenative C(sp 3 )–S Cross-Coupling of Alcohols and Sulfenamides
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00537openalex-snapshot
Activation Strategies for Alkyl Precursors in Achieving C(sp3)–C(sp3) Cross-Coupling via Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03857openalex-snapshot
Photoredox and NHC Enabled Deoxygenative Alcohol Homologation via Formal 1,2-Addition
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00519openalex-snapshot
Nickel-Catalyzed Deoxygenative Amidation of Alcohols with Carbamoyl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02788openalex-snapshot
Ni-Catalyzed Reductive Coupling of Acetals with Anhydrides and Vinyl Triflates via Single-Electron C–O Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03424openalex-snapshot
On-DNA Deoxygenative C(sp 2 )–C(sp 3 ) Coupling Facilitated by Surfactant–DNA (Surf-DNA) Workflow
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03643openalex-snapshot
A Simplified, One-Pot, Procedure for the Deoxygenative Alkylation of Aryl Bromides
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00529openalex-snapshot
Electrochemical N-Centered Radical Cyclization of Aryl Propargyl Alcohols toward Quinolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02310openalex-snapshot
3-Azetidinylpiperidine-4-alkylidenemalononitrile and Related Building Blocks
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02584openalex-snapshot
O -Alkylisourea-Enabled Nickel/Photoredox-Catalyzed Giese Reaction
inferred← citeshttps://doi.org/10.1021/acscatal.4c01857openalex-snapshot
Cross-Double Deoxygenative Carbon–Carbon Bond Formation between Benzyl Benzoates and Allylic Alcohols
inferred← citeshttps://doi.org/10.1021/acscatal.4c03560openalex-snapshot
Alcohols as Alkyl Synthons Enabled by Photoredox-Catalyzed Deoxygenative Activation
inferred← citeshttps://doi.org/10.1021/acscatal.4c06474openalex-snapshot
NHC-Cracker: A Platform for the In Silico Engineering of N-Heterocyclic Carbenes for Diverse Chemical Applications
inferred← citeshttps://doi.org/10.1021/acscatal.5c05860openalex-snapshot
Decarboxylative and Deformylative Alkyl–Alkyl Cross-Coupling Enabled by Nickel/Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.5c07508openalex-snapshot
In Situ Generated Triazine Co-Catalyst Unlocks Amidine Arylation under Dual Nickel/Photoredox Catalysis: A Platform for Mild C–N Bond Formation
inferred← citeshttps://doi.org/10.1021/acscatal.6c04800openalex-snapshot
Metallaphotocatalytic Assembly of Unsymmetrical 1,4-Diketones via Dual Acyl Units: Divergent Initiation of Carboxylic Acids and Aldehydes
inferred← citeshttps://doi.org/10.1021/acscentsci.5c01770openalex-snapshot
Shaking Up Photochemistry: The Future Frontiers of Mechanophotocatalysis
inferred← citeshttps://doi.org/10.1021/acssuschemeng.6c00385openalex-snapshot
A Cobaloxime–Polyoxometalate Conjugate for Enhanced Photocatalytic Tertiary Amine Synthesis
inferred← citeshttps://doi.org/10.1021/jacs.3c05405openalex-snapshot
Rapid and Modular Access to Quaternary Carbons from Tertiary Alcohols via Bimolecular Homolytic Substitution
inferred← citeshttps://doi.org/10.1021/jacs.3c07313openalex-snapshot
Electrochemical Nickel-Catalyzed C(sp3)–C(sp3) Cross-Coupling of Alkyl Halides with Alkyl Tosylates
inferred← citeshttps://doi.org/10.1021/jacs.4c00557openalex-snapshot
Development of a General Organophosphorus Radical Trap: Deoxyphosphonylation of Alcohols
inferred← citeshttps://doi.org/10.1021/jacs.4c02316openalex-snapshot
Engaging Alkenes in Metallaphotoredox: A Triple Catalytic, Radical Sorting Approach to Olefin-Alcohol Cross-Coupling
inferred← citeshttps://doi.org/10.1021/jacs.4c04477openalex-snapshot
Free-Radical Deoxygenative Amination of Alcohols via Copper Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.4c05744openalex-snapshot
Triple Radical Sorting: Aryl-Alkylation of Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.4c08691openalex-snapshot
Electroinduced Reductive and Dearomative Alkene-Aldehyde Coupling
inferred← citeshttps://doi.org/10.1021/jacs.4c14164openalex-snapshot
Harnessing Oxetane and Azetidine Sulfonyl Fluorides for Opportunities in Drug Discovery
inferred← citeshttps://doi.org/10.1021/jacs.4c15827openalex-snapshot
Aryl Acid-Alcohol Cross-Coupling: C(sp 3 )–C(sp 2 ) Bond Formation from Nontraditional Precursors
inferred← citeshttps://doi.org/10.1021/jacs.5c05503openalex-snapshot
Mechanometallaphotoredox Catalysis: Utilizing Increased Throughput Mechanochemistry to Develop Solvent-Minimized Aryl Amination and C(sp2)-C(sp3) Cross-Coupling Reactions with Increased Tolerance to Aerobic Conditions
inferred← citeshttps://doi.org/10.1021/jacs.5c09072openalex-snapshot
Nickel-Catalyzed Enantioconvergent Cross-Electrophile Coupling of Benzylic Alcohols with Alkenyl Electrophiles
inferred← citeshttps://doi.org/10.1021/jacs.5c11065openalex-snapshot
Late-Stage Serine Modification Enables Noncanonical Peptide Synthesis
inferred← citeshttps://doi.org/10.1021/jacs.6c00526openalex-snapshot
Aminyl Radical-Enabled Photoredox/Nickel-Catalyzed C(sp 3 )–C(sp 3 ) Suzuki–Miyaura Cross-Coupling via Halogen-Atom Transfer Strategy
inferred← citeshttps://doi.org/10.1021/jacs.6c09135openalex-snapshot
Piecewise Stereoselective Assembly of Multisubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.6c10795openalex-snapshot
A Unified Platform for Direct Alkynylation from Alcohols via Deoxygenative Metallaphotoredox Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.6c14333openalex-snapshot
A General Photoredox Platform for the Hydroarylation of Olefins
inferred← citeshttps://doi.org/10.1038/s41467-024-45804-zopenalex-snapshot
Metal-free photocatalytic cross-electrophile coupling enables C1 homologation and alkylation of carboxylic acids with aldehydes
inferred← citeshttps://doi.org/10.1038/s41467-024-46713-xopenalex-snapshot
Ni-catalyzed enantioconvergent deoxygenative reductive cross-coupling of unactivated alkyl alcohols and aryl bromides
inferred← citeshttps://doi.org/10.1038/s41467-024-47711-9openalex-snapshot
Dehydroxylative radical N-glycosylation of heterocycles with 1-hydroxycarbohydrates enabled by copper metallaphotoredox catalysis
inferred← citeshttps://doi.org/10.1038/s41467-024-50897-7openalex-snapshot
Deoxygenative radical cross-coupling of C(sp3)−O/C(sp3)−H bonds promoted by hydrogen-bond interaction
inferred← citeshttps://doi.org/10.1038/s41467-025-61639-8openalex-snapshot
Photocatalytic C(sp3)–C(sp3) cross-coupling of carboxylic acids and alkyl halides using a nickel complex and carbon nitride
inferred← citeshttps://doi.org/10.1038/s41467-025-63515-xopenalex-snapshot
Fe-electrocatalytic deoxygenative Giese reaction
inferred← citeshttps://doi.org/10.1038/s41586-024-07987-9openalex-snapshot
Reductive alkyl–alkyl coupling from isolable nickel–alkyl complexes
inferred← citeshttps://doi.org/10.1038/s41929-025-01440-4openalex-snapshot
A stereoselective reductive cross-coupling reaction with kinetic control
inferred← citeshttps://doi.org/10.1038/s42004-024-01363-4openalex-snapshot
Scalable deoxygenative alkynylation of alcohols via flow photochemistry
inferred← citeshttps://doi.org/10.1038/s44160-025-00840-5openalex-snapshot
Nickel-catalysed enantioselective migratory reductive cross-coupling enabled by radical 1,2-amino migration
inferred← citeshttps://doi.org/10.1039/d3ob01066jopenalex-snapshot
NHC-mediated photocatalytic deoxygenation of alcohols for the synthesis of internal alkynes via a Csp 3 –Csp coupling reaction
inferred← citeshttps://doi.org/10.1039/d3qo01059gopenalex-snapshot
A photocatalytic traceless C–N bond formation/cleavage strategy enabling the use of (α-chiral) alkyl aldehydes as deoxygenative (chiral) alkyl radical equivalents
inferred← citeshttps://doi.org/10.1039/d4cc04036hopenalex-snapshot
Dual transition metal electrocatalysis enables selective C(sp3)–C(sp3) bond cleavage and arylation of cyclic alcohols
inferred← citeshttps://doi.org/10.1039/d4ce01002gopenalex-snapshot
C 3 symmetric Ru(N^N) 3 -metalloligand functionalized Zr 6 -organic frameworks for photocatalytic sulfide and amine oxidation
inferred← citeshttps://doi.org/10.1039/d4dt00766bopenalex-snapshot
Aqueous emissive cyclometalated iridium photoreductants: synthesis, computational analysis and the photocatalytic reduction of 4-nitrophenol
inferred← citeshttps://doi.org/10.1039/d4gc02564dopenalex-snapshot
Sustainability in a can: upcycling aluminium scrap in the waste-minimized electrochemical synthesis of 2-oxazoline
inferred← citeshttps://doi.org/10.1039/d4qo00115jopenalex-snapshot
Photoredox catalytic deoxygenative divergent functionalizations of alcohols assisted by N,O-heterocyclic carbenes
inferred← citeshttps://doi.org/10.1039/d4qo00887aopenalex-snapshot
Recent advancements in Ni/photoredox dual catalysis for Csp 3 –Csp 3 cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/d5cs01154jopenalex-snapshot
Enantioselective reductive couplings and related transformations under cooperative photoredox catalysis
inferred← citeshttps://doi.org/10.1039/d5nj04281jopenalex-snapshot
Triphenylphosphine-mediated Ir/Ni dual photoredox–catalyzed C(sp 2 )–C(sp 3 ) coupling of alkyl alcohol and aryl bromide
inferred← citeshttps://doi.org/10.1039/d5ob00193eopenalex-snapshot
A MnCl 2 -catalyzed synthesis of aldehydes from organohalides by using samarium metal in DMF
inferred← citeshttps://doi.org/10.1039/d5qo01215eopenalex-snapshot
Recent advances in light-enabled deoxygenative transformation of alcohols
inferred← citeshttps://doi.org/10.1039/d5sc05919dopenalex-snapshot
Low-valent cobalt catalyzed direct dehydroxylative cross-coupling of benzyl alcohols with aryl-chlorides
inferred← citeshttps://doi.org/10.1039/d6np00024jopenalex-snapshot
Construction of C(sp 3 )–C(sp 3 ) attached ring motifs in natural product synthesis
inferred← citeshttps://doi.org/10.1039/d6ob00803hopenalex-snapshot
Photoredox-catalyzed direct deoxygenative coupling of alcohols to thioethers under batch and flow conditions
inferred← citeshttps://doi.org/10.1039/d6ob01144fopenalex-snapshot
Nickel electrocatalytic C(sp 3 )–C(sp 3 ) cross-coupling from activated carboxylic acids and amines
inferred← citeshttps://doi.org/10.1039/d6qo00086jopenalex-snapshot
mer -Ir(pmp) 3 as a strongly photoreducing and stable Ir(C^C) 3 photocatalyst for metallaphotoredox catalysis
inferred← citeshttps://doi.org/10.1055/a-2456-4566openalex-snapshot
Investigating the Photoactivity of Low-Valent Zirconium Catalyst in Ether Activation
inferred← citeshttps://doi.org/10.1055/s-0042-1751889openalex-snapshot
Alcohols as Substrates for Metallaphotoredox-Catalyzed C(sp3)–C(sp3) Cross-Coupling
inferred← citeshttps://doi.org/10.1093/bulcsj/uoad003openalex-snapshot
Nickel-catalyzed cross-coupling between benzyl alcohols and alkenyl triflates assisted by titanium-mediated radical C–O bond cleavage
inferred← citeshttps://doi.org/10.1126/science.adl5890openalex-snapshot
Alcohol-alcohol cross-coupling enabled by S H 2 radical sorting
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4006707/v1openalex-snapshot
Deoxygenative radical cross-coupling of C(sp3)−O/C(sp3)−H bonds enabled by hydrogen-bond interaction
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.83.858openalex-snapshot
Generating Carbon Radicals Through Alcohol C-O Bond Cleavage
inferred← citeshttps://doi.org/10.6023/cjoc202504001openalex-snapshot
Recent Progress on the Construction of C(sp 2 )—C(sp 3 ) Bonds via Photoredox/Nickel Dual Catalysis
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.