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Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1099-0690(199909)1999:9<2079::aid-ejoc2079>3.0.co;2-dopenalex-snapshot
A Facile Route to Bridgehead Disubstituted Bicyclo[1.1.1]pentanes Involving Palladium-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1002/0471264180.or079.01openalex-snapshot
Cross‐Coupling Reactions of Organotrifluoroborate Salts
inferredcites →https://doi.org/10.1002/1099-0690(200004)2000:7<1137::aid-ejoc1137>3.0.co;2-2openalex-snapshot
Nickel- and Palladium-Catalyzed Cross-Coupling Reactions at the Bridgehead of Bicyclo[1.1.1]pentane Derivatives - A Convenient Access to Liquid Crystalline Compounds Containing Bicyclo[1.1.1]pentane Moieties
inferredcites →https://doi.org/10.1002/anie.201207343openalex-snapshot
Chiral Copper(II)‐Catalyzed Enantioselective Boron Conjugate Additions to α,β‐Unsaturated Carbonyl Compounds in Water
inferredcites →https://doi.org/10.1002/anie.201706799openalex-snapshot
Synthesis of Bicyclo[1.1.1]pentane Bioisosteres of Internal Alkynes and para ‐Disubstituted Benzenes from [1.1.1]Propellane
inferredcites →https://doi.org/10.1002/anie.201809431openalex-snapshot
Alkyl Carbon–Carbon Bond Formation by Nickel/Photoredox Cross‐Coupling
inferredcites →https://doi.org/10.1002/anie.201909655openalex-snapshot
Silaboration of [1.1.1]Propellane: A Storable Feedstock for Bicyclo[1.1.1]pentane Derivatives
inferredcites →https://doi.org/10.1002/anie.201914875openalex-snapshot
1,3‐Difunctionalizations of [1.1.1]Propellane via 1,2‐Metallate Rearrangements of Boronate Complexes
inferredcites →https://doi.org/10.1002/anie.202000140openalex-snapshot
Divergent Strain‐Release Amino‐Functionalization of [1.1.1]Propellane with Electrophilic Nitrogen‐Radicals
inferredcites →https://doi.org/10.1002/anie.202004090openalex-snapshot
Synthesis of All‐Carbon Disubstituted Bicyclo[1.1.1]pentanes by Iron‐Catalyzed Kumada Cross‐Coupling
inferredcites →https://doi.org/10.1002/anie.202009340openalex-snapshot
Highly Regioselective Addition of Allylic Zinc Halides and Various Zinc Enolates to [1.1.1]Propellane
inferredcites →https://doi.org/10.1002/cmdc.201402502openalex-snapshot
Evaluation of tert‐Butyl Isosteres: Case Studies of Physicochemical and Pharmacokinetic Properties, Efficacies, and Activities
inferredcites →https://doi.org/10.1016/j.chempr.2017.05.008openalex-snapshot
Recent Developments in Organoboron Chemistry: Old Dogs, New Tricks
inferredcites →https://doi.org/10.1016/j.tet.2011.10.004openalex-snapshot
Radical reactions on pinene-oxide derivatives induced by Ti(III)
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.joc.5b00981openalex-snapshot
Organotrifluoroborates: Another Branch of the Mighty Oak
inferredcites →https://doi.org/10.1021/acs.orglett.0c00242openalex-snapshot
Continuous Flow-Enabled Synthesis of Bench-Stable Bicyclo[1.1.1]pentane Trifluoroborate Salts and Their Utilization in Metallaphotoredox Cross-Couplings
inferredcites →https://doi.org/10.1021/acs.orglett.1c01558openalex-snapshot
Nickel-Catalyzed Decarboxylative Cross-Coupling of Bicyclo[1.1.1]pentyl Radicals Enabled by Electron Donor–Acceptor Complex Photoactivation
inferredcites →https://doi.org/10.1021/acsmedchemlett.6b00281openalex-snapshot
Investigation of a Bicyclo[1.1.1]pentane as a Phenyl Replacement within an LpPLA 2 Inhibitor
inferredcites →https://doi.org/10.1021/cr0509758openalex-snapshot
Potassium Organotrifluoroborates: New Perspectives in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr100233ropenalex-snapshot
Chemistry and Biology Of Multicomponent Reactions
inferredcites →https://doi.org/10.1021/cr950066qopenalex-snapshot
Bioisosterism: A Rational Approach in Drug Design
inferredcites →https://doi.org/10.1021/ja00343a025openalex-snapshot
Strain energies of small ring propellanes
inferredcites →https://doi.org/10.1021/ja208068wopenalex-snapshot
Room-Temperature C–H Arylation: Merger of Pd-Catalyzed C–H Functionalization and Visible-Light Photocatalysis
inferredcites →https://doi.org/10.1021/jacs.0c02355openalex-snapshot
On the Nature of C(sp3)–C(sp2) Bond Formation in Nickel-Catalyzed Tertiary Radical Cross-Couplings: A Case Study of Ni/Photoredox Catalytic Cross-Coupling of Alkyl Radicals and Aryl Halides
inferredcites →https://doi.org/10.1021/jacs.0c08823openalex-snapshot
General Method for Enantioselective Three-Component Carboarylation of Alkenes Enabled by Visible-Light Dual Photoredox/Nickel Catalysis
inferredcites →https://doi.org/10.1021/jacs.0c11964openalex-snapshot
Practical and Modular Construction of C(sp 3 )-Rich Alkyl Boron Compounds
inferredcites →https://doi.org/10.1021/jacs.0c13077openalex-snapshot
Photochemical C–H Activation Enables Nickel-Catalyzed Olefin Dicarbofunctionalization
inferredcites →https://doi.org/10.1021/jacs.6b07172openalex-snapshot
Redox-Active Esters in Fe-Catalyzed C–C Coupling
inferredcites →https://doi.org/10.1021/jacs.7b06288openalex-snapshot
Enabling the Cross-Coupling of Tertiary Organoboron Nucleophiles through Radical-Mediated Alkyl Transfer
inferredcites →https://doi.org/10.1021/jacs.7b11865openalex-snapshot
Radical Multicomponent Carboamination of [1.1.1]Propellane
inferredcites →https://doi.org/10.1021/jacs.9b08282openalex-snapshot
Three-Component Olefin Dicarbofunctionalization Enabled by Nickel/Photoredox Dual Catalysis
inferredcites →https://doi.org/10.1021/jm101356popenalex-snapshot
Improvement in Aqueous Solubility in Small Molecule Drug Discovery Programs by Disruption of Molecular Planarity and Symmetry
inferredcites →https://doi.org/10.1021/jm1013693openalex-snapshot
Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design
inferredcites →https://doi.org/10.1021/jm300094uopenalex-snapshot
Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor
inferredcites →https://doi.org/10.1021/ol201900dopenalex-snapshot
Copper-Catalyzed β-Boration of α,β-Unsaturated Carbonyl Compounds with Tetrahydroxydiborane
inferredcites →https://doi.org/10.1038/nature14006openalex-snapshot
Functionalized olefin cross-coupling to construct carbon–carbon bonds
inferredcites →https://doi.org/10.1038/s41570-017-0052openalex-snapshot
The merger of transition metal and photocatalysis
inferredcites →https://doi.org/10.1038/s41586-020-2060-zopenalex-snapshot
Copper-mediated synthesis of drug-like bicyclopentanes
inferredcites →https://doi.org/10.1039/d1sc01349aopenalex-snapshot
Strain-release 2-azaallyl anion addition/borylation of [1.1.1]propellane: synthesis and functionalization of benzylamine bicyclo[1.1.1]pentyl boronates
inferredcites →https://doi.org/10.1126/science.1253647openalex-snapshot
Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis
inferredcites →https://doi.org/10.1126/science.aan3679openalex-snapshot
Photoinduced decarboxylative borylation of carboxylic acids
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.202300534openalex-snapshot
Multicomponent Radical Cross‐Coupling Reaction of [1.1.1]Propellane: Synthesis of 1‐Arylthiol‐3‐Heteroaryl Bicyclo[1.1.1]pentanes †
inferred← citeshttps://doi.org/10.1002/adsc.70765openalex-snapshot
Photochemical Strategies for the Synthesis of C ‐Disubstituted Bicyclo[1.1.1]pentanes via Direct Difunctionalization of [1.1.1]Propellane: A Review
inferred← citeshttps://doi.org/10.1002/ajoc.202300275openalex-snapshot
Recent Advances in Carbonyl‐Photoredox/Transition Metal Dual Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202302223openalex-snapshot
A General and Practical Route to Functionalized Bicyclo[1.1.1]Pentane‐Heteroaryls Enabled by Photocatalytic Multicomponent Heteroarylation of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/ange.202303435openalex-snapshot
Synthesis of Bicyclo[1.1.1]pentane (BCP)‐Based Straight‐Shaped Diphosphine Ligands**
inferred← citeshttps://doi.org/10.1002/ange.202304246openalex-snapshot
General Synthesis of 3‐Azabicyclo[3.1.1]heptanes and Evaluation of Their Properties as Saturated Isosteres**
inferred← citeshttps://doi.org/10.1002/ange.202305043openalex-snapshot
Katalytische formale [2π+2σ]‐Cycloaddition von Aldehyden mit Bicyclobutanen: Zweckmäßiger Zugang zu polysubstituierten 2‐Oxabicyclo[2.1.1]hexanen
inferred← citeshttps://doi.org/10.1002/ange.202306498openalex-snapshot
Group 14 Elements Hetero‐Difunctionalizations via Nickel‐Catalyzed Electroreductive Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/ange.202310066openalex-snapshot
Silver‐Catalyzed Dearomative [2π+2σ] Cycloadditions of Indoles with Bicyclobutanes: Access to Indoline Fused Bicyclo[2.1.1]hexanes**
inferred← citeshttps://doi.org/10.1002/ange.202314700openalex-snapshot
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
inferred← citeshttps://doi.org/10.1002/ange.202317333openalex-snapshot
Light‐Driven Synthesis and Functionalization of Bicycloalkanes, Cubanes and Related Bioisosteres
inferred← citeshttps://doi.org/10.1002/ange.202318476openalex-snapshot
Eu(OTf)3‐Catalyzed Formal Dipolar [4π+2σ] Cycloaddition of Bicyclo‐[1.1.0]butanes with Nitrones: Access to Polysubstituted 2‐Oxa‐3‐azabicyclo[3.1.1]heptanes
inferred← citeshttps://doi.org/10.1002/ange.202400494openalex-snapshot
Photoinduced C(sp3)−H Bicyclopentylation Enabled by an Electron Donor–Acceptor Complex‐Mediated Chemoselective Three‐Component Radical Relay
inferred← citeshttps://doi.org/10.1002/ange.202402730openalex-snapshot
Silver‐Enabled Cycloaddition of Bicyclobutanes with Isocyanides for the Synthesis of Polysubstituted 3‐Azabicyclo[3.1.1]heptanes
inferred← citeshttps://doi.org/10.1002/ange.202411961openalex-snapshot
Halogen Bonding Initiated Difunctionalization of [1.1.1]Propellane via Photoinduced Polarity Match Additions
inferred← citeshttps://doi.org/10.1002/ange.202420831openalex-snapshot
Diverse Synthesis of Arene‐Fused [n.1.1]‐Bridged Molecules via Catalytic Cycloaddition and Rearrangement Reactions
inferred← citeshttps://doi.org/10.1002/ange.2936884openalex-snapshot
A d e ‐ n ovo Approach Towards Divergent [3+2π/σ] Photocycloadditions of Nitrones via Assembly‐Controlled Kinetic Electron Transfer Gating
inferred← citeshttps://doi.org/10.1002/anie.202302223openalex-snapshot
A General and Practical Route to Functionalized Bicyclo[1.1.1]Pentane‐Heteroaryls Enabled by Photocatalytic Multicomponent Heteroarylation of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/anie.202303435openalex-snapshot
Synthesis of Bicyclo[1.1.1]pentane (BCP)‐Based Straight‐Shaped Diphosphine Ligands**
inferred← citeshttps://doi.org/10.1002/anie.202304246openalex-snapshot
General Synthesis of 3‐Azabicyclo[3.1.1]heptanes and Evaluation of Their Properties as Saturated Isosteres**
inferred← citeshttps://doi.org/10.1002/anie.202305043openalex-snapshot
Catalytic Formal [2π+2σ] Cycloaddition of Aldehydes with Bicyclobutanes: Expedient Access to Polysubstituted 2‐Oxabicyclo[2.1.1]hexanes
inferred← citeshttps://doi.org/10.1002/anie.202306498openalex-snapshot
Group 14 Elements Hetero‐Difunctionalizations via Nickel‐Catalyzed Electroreductive Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/anie.202310066openalex-snapshot
Silver‐Catalyzed Dearomative [2π+2σ] Cycloadditions of Indoles with Bicyclobutanes: Access to Indoline Fused Bicyclo[2.1.1]hexanes**
inferred← citeshttps://doi.org/10.1002/anie.202314700openalex-snapshot
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
inferred← citeshttps://doi.org/10.1002/anie.202317333openalex-snapshot
Light‐Driven Synthesis and Functionalization of Bicycloalkanes, Cubanes and Related Bioisosteres
inferred← citeshttps://doi.org/10.1002/anie.202318476openalex-snapshot
Eu(OTf)3‐Catalyzed Formal Dipolar [4π+2σ] Cycloaddition of Bicyclo‐[1.1.0]butanes with Nitrones: Access to Polysubstituted 2‐Oxa‐3‐azabicyclo[3.1.1]heptanes
inferred← citeshttps://doi.org/10.1002/anie.202400494openalex-snapshot
Photoinduced C(sp3)−H Bicyclopentylation Enabled by an Electron Donor–Acceptor Complex‐Mediated Chemoselective Three‐Component Radical Relay
inferred← citeshttps://doi.org/10.1002/anie.202402730openalex-snapshot
Silver‐Enabled Cycloaddition of Bicyclobutanes with Isocyanides for the Synthesis of Polysubstituted 3‐Azabicyclo[3.1.1]heptanes
inferred← citeshttps://doi.org/10.1002/anie.202411961openalex-snapshot
Halogen Bonding Initiated Difunctionalization of [1.1.1]Propellane via Photoinduced Polarity Match Additions
inferred← citeshttps://doi.org/10.1002/anie.202420831openalex-snapshot
Diverse Synthesis of Arene‐Fused [n.1.1]‐Bridged Molecules via Catalytic Cycloaddition and Rearrangement Reactions
inferred← citeshttps://doi.org/10.1002/anie.2936884openalex-snapshot
A d e ‐ n ovo Approach Towards Divergent [3+2π/σ] Photocycloadditions of Nitrones via Assembly‐Controlled Kinetic Electron Transfer Gating
inferred← citeshttps://doi.org/10.1002/chem.202303504openalex-snapshot
[3+2] Cycloaddition of Alkynyl Boronates and in situ Generated Azomethine Ylide
inferred← citeshttps://doi.org/10.1002/chem.202402152openalex-snapshot
Uncatalyzed Diboron Activation by a Strained Hydrocarbon: Experimental and Theoretical Study of [1.1.1]Propellane Diborylation
inferred← citeshttps://doi.org/10.1002/cjoc.70244openalex-snapshot
Synthesis of 1‐Chalcogen‐3‐Alkyl Bicyclo[1.1.1]pentanes Enabled by a Photocatalytic Multicomponent Radical Coupling
inferred← citeshttps://doi.org/10.1002/cjoc.70352openalex-snapshot
Nickel‐Catalyzed Modular Four‐Component 1,3‐Alkylcarbonylation of σ Bonds in Bicyclo[1.1.0]butanes via Ring Strain Effect
inferred← citeshttps://doi.org/10.1002/cjoc.70595openalex-snapshot
Visible‐Light Catalyzed Functionalizations of Allylic C–H Bonds
inferred← citeshttps://doi.org/10.1002/cjoc.70766openalex-snapshot
Visible‐Light‐Promoted Four‐Component Reaction Based on Catalytic EDA Complexes: Efficient Synthesis of C3 ‐Functionalized Bicyclo[1.1.1]pentane Sulfones
inferred← citeshttps://doi.org/10.1002/ejoc.202400386openalex-snapshot
EDA Complex from BCP‐Thianthrenium Salt: A Catalyst‐Free Strategy To Access 1‐Trifluoromethyl‐3‐quinoxaline Derivatives Bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1002/tcr.202300256openalex-snapshot
Chemoselective Reactions of Functionalized Sulfonyl Halides
inferred← citeshttps://doi.org/10.1002/tcr.202500018openalex-snapshot
Photocatalytic Difunctionalization of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1007/s11426-023-1715-2openalex-snapshot
Iodopentafluorosulfanylation of [1.1.1]propellane and further functionalizations
inferred← citeshttps://doi.org/10.1007/s11426-024-1973-2openalex-snapshot
Nickel-catalyzed carbonylative four-component 1,4-dicarbofunctionalization of 1,3-enynes
inferred← citeshttps://doi.org/10.1007/s11426-025-3149-2openalex-snapshot
Controlled ring-opening of [1.1.1]propellane with aryl catecholato boronates to form monomeric and dimeric methylenecyclobutanes
inferred← citeshttps://doi.org/10.1007/s41061-025-00490-3openalex-snapshot
Recent Advances in Radical Coupling Reactions Directly Involving Bicyclo[1.1.1]pentane (BCP)
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.112641openalex-snapshot
Modular synthesis of functionalized heteroarylated-bicyclo[1.1.1]pentane via photochemical iron catalysis
inferred← citeshttps://doi.org/10.1016/j.checat.2023.100608openalex-snapshot
Nickel-mediated alkyl-, acyl-, and sulfonylcyanation of [1.1.1]propellane
inferred← citeshttps://doi.org/10.1016/j.checat.2023.100618openalex-snapshot
Synthesis of BCP nitriles enabled by a metallaphotoredox-based multi-component reaction
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.tchem.2024.100070openalex-snapshot
Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes
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.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.4c01422openalex-snapshot
Visible Light-Induced, Nickel-Catalyzed Late-Stage 4-Alkylation of Hantzsch Esters with Alkyl Bromide
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01605openalex-snapshot
Amine-Borane-Mediated, Nickel/Photoredox-Catalyzed Cross-Electrophile Coupling between Alkyl and Aryl Bromides
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02941openalex-snapshot
Multicomponent Synthesis of Alkyl BCP-Heteroaryls via Electron Donor–Acceptor Complex Photoactivation under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01558openalex-snapshot
Unlocking the Accessibility of Alkyl/Aryl Radicals from Boronic Acids through EDA Complex Photoactivation
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01751openalex-snapshot
Iron-Catalyzed Radical Cascade Multicomponent Coupling: Expedient Synthesis of Diverse Allenes from 1,3-Enynes
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02501openalex-snapshot
Construction of Bridged N,O -Heterocycles via Palladium-Catalyzed [5 + 4] Cycloadditions of Azabicyclo[2.1.0]pentanes and Vinyl Oxiranes
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02790openalex-snapshot
Synthesis of Imidized Cyclobutene Derivatives by Strain Release of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02875openalex-snapshot
Synthesis of Sulfur-Substituted Bicyclo[1.1.1]pentanes by Iodo-Sulfenylation of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00307openalex-snapshot
General Method for Selective Three-Component Carboacylation of Alkenes via Visible-Light Dual Photoredox/Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01512openalex-snapshot
Intermolecular Formal [2π + 2σ] Cycloaddition of Enol Silyl Ethers with Bicyclo[1.1.0]butanes Promoted by Lewis Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01981openalex-snapshot
Ni-Catalyzed Reductive 1,2-Alkylarylation of Alkenes for the Synthesis of Spirocyclic γ-Lactams
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02171openalex-snapshot
Light-Induced, Cs2CO3 Promoted C–S Cleavage of Heteroaryl Sulfones for Benzyl Heteroarylation of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02476openalex-snapshot
Photocatalyzed 1,3-Bromodifluoroallylation of [1.1.1]Propellane with α-Trifluoromethylalkenes and KBr Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02969openalex-snapshot
Site-Specific Radical Alkylation of Aryl Cyanide: Visible-Light, Photoredox-Catalyzed, Three-Component Arylalkylation of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03198openalex-snapshot
Photocatalytic Diheteroarylation of [1.1.1]Propellane for the Construction of 1,3-Diheteroaryl Bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03316openalex-snapshot
Direct Diazoarylation of [1.1.1]Propellane with Arenediazonium Salts: A Modular Assembly of Arylated Diazo Bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03429openalex-snapshot
Benzyl Alcohol Functionalization of [1.1.1]Propellane with Alkanes and Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00882openalex-snapshot
Photoredox/Copper Cooperatively Catalyzed Arylalkynylation of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01849openalex-snapshot
Dicarbofunctionalization of [1.1.1]Propellane: One-Step Multicomponent Approach to BCP-Aryl Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02589openalex-snapshot
Multiatom Skeletal Editing to Access SeCN-Containing Bicyclo[1.1.1]pentanes with Antitumor Activity
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03592openalex-snapshot
Visible-Light-Induced Regio- and Stereoselective C(sp2)-H Trifluoromethyl-Bicyclopentylation of Enamides with BCP-Thianthrenium Salt via Oxidative Radical/Polar Crossover
inferred← citeshttps://doi.org/10.1021/acscatal.2c03498openalex-snapshot
General and Practical Route to Diverse 1-(Difluoro)alkyl-3-aryl Bicyclo[1.1.1]pentanes Enabled by an Fe-Catalyzed Multicomponent Radical Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1021/acscatal.3c00567openalex-snapshot
Theoretical Underpinning of Synergetic Ir/Cu-Metallaphotoredox Catalysis in Multicomponent C–N Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.3c02339openalex-snapshot
Metal-Free Photoinduced Acylboration of [1.1.1]Propellane via Energy Transfer Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.3c05003openalex-snapshot
General and Modular Route to (Halo)alkyl BCP-Heteroaryls Enabled by α-Aminoalkyl Radical-Mediated Halogen-Atom Transfer
inferred← citeshttps://doi.org/10.1021/acscatal.4c00533openalex-snapshot
Photocatalyzed Dual Strain Release of [1.1.1]Propellane with Diazo Compounds
inferred← citeshttps://doi.org/10.1021/acscatal.4c00740openalex-snapshot
Synthesis of 1-(Halo)alkyl-3-heteroaryl Bicyclo[1.1.1]pentanes Enabled by a Photocatalytic Minisci-type Multicomponent Reaction
inferred← citeshttps://doi.org/10.1021/acscatal.5c04227openalex-snapshot
Ni-Catalyzed Carbonylative Four-Component Spirocyclization Cascade of BCB-Tethered Allyl Amides and Esters
inferred← citeshttps://doi.org/10.1021/acscatal.6c01419openalex-snapshot
Decarboxylative C(sp 2 )−C(sp 3 ) Cross-Coupling of Bicyclo[1.1.1]pentane and Cubane Carboxylic Acids Using a Nickel(II) Aryl Precatalyst
inferred← citeshttps://doi.org/10.1021/acscatal.6c02845openalex-snapshot
Incorporation of C(sp3)-Rich Benzene Bioisosteres via Iron-Catalyzed Photoelectrochemical Decarboxylative C−H Functionalization
inferred← citeshttps://doi.org/10.1021/jacs.2c09248openalex-snapshot
Synthesis of Polysubstituted 2-Oxabicyclo[2.1.1]hexanes via Visible-Light-Induced Energy Transfer
inferred← citeshttps://doi.org/10.1021/jacs.2c11501openalex-snapshot
Photochemical Intermolecular [3σ + 2σ]-Cycloaddition for the Construction of Aminobicyclo[3.1.1]heptanes
inferred← citeshttps://doi.org/10.1021/jacs.2c13298openalex-snapshot
A General and Modular Approach to BCP Alkylamines via Multicomponent Difunctionalization of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/jacs.3c02745openalex-snapshot
Photoredox Cleavage of a Csp3–Csp3 Bond in Aromatic Hydrocarbons
inferred← citeshttps://doi.org/10.1021/jacs.3c10024openalex-snapshot
Bicyclopentylation of Alcohols with Thianthrenium Reagents
inferred← citeshttps://doi.org/10.1021/jacs.4c10123openalex-snapshot
Copper-Catalyzed Enantioselective [4π + 2σ] Cycloaddition of Bicyclobutanes with Nitrones
inferred← citeshttps://doi.org/10.1021/jacs.6c12832openalex-snapshot
Synthesis, Evaluation, and Context for Applications of SF5-Containing [1.1.1]Bicyclopentane and [ 2 ]Staffane “Hybrid Bioisosteres”
inferred← citeshttps://doi.org/10.1021/jacsau.3c00014openalex-snapshot
Conquering the Synthesis and Functionalization of Bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1021/jacsau.4c00347openalex-snapshot
Strain-Releasing Ring-Opening Diphosphinations for the Synthesis of Diphosphine Ligands with Cyclic Backbones
inferred← citeshttps://doi.org/10.1038/s41467-024-50356-3openalex-snapshot
1,3-Difunctionalization of [1.1.1]propellane through iron-hydride catalyzed hydropyridylation
inferred← citeshttps://doi.org/10.1038/s41467-025-61017-4openalex-snapshot
Electro-oxidative amination of benzylic C(sp³)–C(sp³) bonds in aromatic hydrocarbons
inferred← citeshttps://doi.org/10.1038/s41467-026-68309-3openalex-snapshot
Propellane-free access to bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1038/s41557-023-01222-0openalex-snapshot
2-Oxabicyclo[2.1.1]hexanes as saturated bioisosteres of the ortho-substituted phenyl ring
inferred← citeshttps://doi.org/10.1038/s44160-023-00277-8openalex-snapshot
O-, N- and C-bicyclopentylation using thianthrenium reagents
inferred← citeshttps://doi.org/10.1038/s44160-023-00349-9openalex-snapshot
Electrochemical chemo- and regioselective arylalkylation, dialkylation and hydro(deutero)alkylation of 1,3-enynes
inferred← citeshttps://doi.org/10.1038/s44160-024-00637-yopenalex-snapshot
Light-enabled scalable synthesis of bicyclo[1.1.1]pentane halides and their functionalizations
inferred← citeshttps://doi.org/10.1038/s44160-025-00745-3openalex-snapshot
Difunctionalization of bicyclo[1.1.0]butanes enabled by merging C−C cleavage and ruthenium-catalysed remote C−H activation
inferred← citeshttps://doi.org/10.1038/s44160-025-00821-8openalex-snapshot
Thianthrenium-enabled modular synthesis of bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1039/d2gc04521dopenalex-snapshot
Visible-light-induced direct perfluoroalkylation/heteroarylation of [1.1.1]propellane to diverse bicyclo[1.1.1]pentanes (BCPs) under metal and photocatalyst-free conditions
inferred← citeshttps://doi.org/10.1039/d2gc04683kopenalex-snapshot
Synthesis of 1-perfluoroalkyl-3-heteroaryl bicyclo[1.1.1]pentanes via visible light-induced and metal-free perfluoroalkylation of [1.1.1]propellane
inferred← citeshttps://doi.org/10.1039/d2sc05100aopenalex-snapshot
One step synthesis of unsymmetrical 1,3-disubstituted BCP ketones via nickel/photoredox-catalyzed [1.1.1]propellane multicomponent dicarbofunctionalization
inferred← citeshttps://doi.org/10.1039/d3gc00643copenalex-snapshot
Visible light-induced synthesis of 1,3-disubstituted bicyclo[1.1.1]pentane ketones via cooperative photoredox and N-heterocyclic carbene catalysis
inferred← citeshttps://doi.org/10.1039/d3gc01633aopenalex-snapshot
Modular construction of N -arylated amino acid esters enabled by a photoredox-catalyzed multicomponent reaction
inferred← citeshttps://doi.org/10.1039/d3ob01036hopenalex-snapshot
Synthesis of 1,3-disubstituted bicyclo[1.1.1]pentanes by cross-coupling induced by transition metals – formation of C–C bonds
inferred← citeshttps://doi.org/10.1039/d3qo01019hopenalex-snapshot
Photocatalyzed radical multicomponent alkylacylation of [1.1.1]propellane to synthesize 1,3-disubstituted BCP ketones
inferred← citeshttps://doi.org/10.1039/d4gc01015aopenalex-snapshot
Metal- and photocatalyst-free three-component strategy to prepare benzylalcohol-, aldehyde-substituted BCP building blocks
inferred← citeshttps://doi.org/10.1039/d4ob01020eopenalex-snapshot
Photochemical tandem reaction of nitrogen containing heterocycles, bicyclo[1.1.1]pentane, and difluoroiodane( iii ) reagents
inferred← citeshttps://doi.org/10.1039/d4qo01351dopenalex-snapshot
Transition-metal-, oxidant- and additive-free multi-component synthesis of alkyl heteroaryl BCPs enabled by visible-light-induced phosphine-catalyzed halogen-atom transfer
inferred← citeshttps://doi.org/10.1039/d4sc08280jopenalex-snapshot
Silver-mediated formal [4π + 2 σ ] cycloaddition reactions of bicyclobutanes with nitrile imines: access to 2,3-diazobicyclo[3.1.1]heptenes
inferred← citeshttps://doi.org/10.1039/d5cc01948fopenalex-snapshot
Site-selective alkylation of electron-deficient aromatic cycles: visible-light photoredox-catalyzed radical di-functionalization of [1.1.1]propellane
inferred← citeshttps://doi.org/10.1039/d5cc05977aopenalex-snapshot
Ru-catalyzed C–H annulation: accessing quinazolinone–BCP hybrids from stable precursors
inferred← citeshttps://doi.org/10.1039/d5gc02067kopenalex-snapshot
Sustainable synthesis of 1-thiol-3-alkyl bicyclo[1.1.1]pentanes via electron donor–acceptor complex photoactivation: a metal- and additive-free strategy for bioisostere design
inferred← citeshttps://doi.org/10.1039/d5qo00357aopenalex-snapshot
Metal and photocatalyst-free alkylboration of [1.1.1]propellane enabled by red-light-induced electron transfer
inferred← citeshttps://doi.org/10.1039/d6qo00901hopenalex-snapshot
Light-enabled metal-free carbo- and silyl functionalization of [1.1.1]propellane and [3.1.1]propellane
inferred← citeshttps://doi.org/10.1039/d6sc00382fopenalex-snapshot
Photocatalytic multicomponent alkene dicarbofunctionalization via PCET/nickel dual catalysis
inferred← citeshttps://doi.org/10.1055/s-0042-1752983openalex-snapshot
Photoredox Cross-Coupling for Propellane-Curious Chemists
inferred← citeshttps://doi.org/10.1126/sciadv.aea8588openalex-snapshot
Nickel-catalyzed radical relay enabled chemoselective fluoroalkyl-borylation of [1.1.1]propellane under kinetic control
inferred← citeshttps://doi.org/10.2174/0115701794347153241107110324openalex-snapshot
Metal- and Photocatalyst-Free Sulfonylcyanation of [1.1.1]Propellane with Sulfonyl Cyanide
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-8dclmopenalex-snapshot
The LARGEST library of Bicyclo[1.1.1]pentanes for Drug Discovery enabled by Light
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-jbb0ropenalex-snapshot
Unexpected Discovery of Saturated Pyridine Mimetics
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-qkzmkopenalex-snapshot
Silver-Catalyzed Dearomative [2π+2σ] Cycloadditions of Indoles with Bicyclobutanes: Expedient Access to Indoline Fused Bicy-clo[2.1.1]hexanes
inferred← citeshttps://doi.org/10.6023/cjoc202400014openalex-snapshot
Synthesis of (Halo)alkyl Bicyclo[1.1.1]pentane (BCP)-Heteroaryls Enabled by α-Aminoalkyl Radical-Mediated Halogen-Atom Transfer
inferred← citeshttps://doi.org/10.6023/cjoc202601034openalex-snapshot
Recent Advances in the Light-Driven One-Step Synthesis of Dual Carbon-Substituted Bicyclo[1.1.1]pentanes
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