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Dual Ni/Organophotoredox Catalyzed Allylative Ring Opening Reaction of Oxabenzonorbornadienes and Analogs

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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/adsc.200700324openalex-snapshot
The Development of the Asymmetric Nozaki–Hiyama–Kishi Reaction
inferredcites →https://doi.org/10.1002/adsc.201300910openalex-snapshot
Nickel‐Catalyzed Regio‐ and Stereoselective Reductive Coupling of Oxa‐ and Azabicyclic Alkenes with Enones and Electron‐Rich Alkynes
inferredcites →https://doi.org/10.1002/adsc.202001250openalex-snapshot
Catalytic Photoredox Allylation of Aldehydes Promoted by a Cobalt Complex
inferredcites →https://doi.org/10.1002/ange.202103479openalex-snapshot
Expedient Dual Co/Organophotoredox Catalyzed Stereoselective Synthesis of All‐Carbon Quaternary Centers
inferredcites →https://doi.org/10.1002/anie.201409999openalex-snapshot
Redox‐Neutral α‐Allylation of Amines by Combining Palladium Catalysis and Visible‐Light Photoredox Catalysis
inferredcites →https://doi.org/10.1002/anie.201506003openalex-snapshot
Cobalt‐Catalyzed Allylation of Heterobicyclic Alkenes: Ligand‐Induced Divergent Reactivities
inferredcites →https://doi.org/10.1002/anie.202114981openalex-snapshot
Nickel‐Mediated Enantioselective Photoredox Allylation of Aldehydes with Visible Light
inferredcites →https://doi.org/10.1002/chem.200701775openalex-snapshot
Concise Enantioselective Total Syntheses of (+)‐Homochelidonine, (+)‐Chelamidine, (+)‐Chelidonine, (+)‐Chelamine and (+)‐Norchelidonine by a Pd II ‐Catalyzed Ring‐Opening Strategy
inferredcites →https://doi.org/10.1002/cjoc.202100622openalex-snapshot
Cobalt‐Catalyzed Enantioselec tive Ring‐Opening Reactions of Oxa‐ and Aza‐bicyclic Alkenes with Alkenylboronic Acids
inferredcites →https://doi.org/10.1002/ejoc.200700054openalex-snapshot
Stereoselective Carbonyl Allylation by Umpolung of Allylpalladium(II) Complexes
inferredcites →https://doi.org/10.1016/j.bmcl.2008.12.095openalex-snapshot
Discovery of μ-opioid selective ligands derived from 1-aminotetralin scaffolds made via metal-catalyzed ring-opening reactions
inferredcites →https://doi.org/10.1016/j.chempr.2020.10.020openalex-snapshot
Transition-metal-catalyzed C–H allylation reactions
inferredcites →https://doi.org/10.1016/j.tetlet.2006.06.134openalex-snapshot
Iron-catalyzed allylation of ketones
inferredcites →https://doi.org/10.1016/s0040-4020(99)00456-1openalex-snapshot
Selective functionalization of 1,2-dihydronaphthalenols leads to a concise, stereoselective synthesis of sertraline
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00144openalex-snapshot
Role of the Nozaki–Hiyama–Takai–Kishi Reaction in the Synthesis of Natural Products
inferredcites →https://doi.org/10.1021/acs.orglett.0c00593openalex-snapshot
Aminomethylation of Oxabenzonorbornadienes via the Merger of Photoredox and Nickel Catalysis
inferredcites →https://doi.org/10.1021/acscatal.0c00348openalex-snapshot
Cp2TiCl2-Catalyzed Photoredox Allylation of Aldehydes with Visible Light
inferredcites →https://doi.org/10.1021/acscatal.0c03697openalex-snapshot
Direct Access to Monoprotected Homoallylic 1,2-Diols via Dual Chromium/Photoredox Catalysis
inferredcites →https://doi.org/10.1021/acscatal.0c05330openalex-snapshot
Photocatalytic Umpolung Synthesis of Nucleophilic π-Allylcobalt Complexes for Allylation of Aldehydes
inferredcites →https://doi.org/10.1021/acscatal.5b02204openalex-snapshot
Donor–Acceptor Fluorophores for Visible-Light-Promoted Organic Synthesis: Photoredox/Ni Dual Catalytic C(sp 3 )–C(sp 2 ) Cross-Coupling
inferredcites →https://doi.org/10.1021/acscatal.9b03695openalex-snapshot
Inversion of Enantioselectivity in Allene Gas versus Allyl Acetate Reductive Aldehyde Allylation Guided by Metal-Centered Stereogenicity: An Experimental and Computational Study
inferredcites →https://doi.org/10.1021/acscatal.9b04222openalex-snapshot
Dialkylation of 1,3-Dienes by Dual Photoredox and Chromium Catalysis
inferredcites →https://doi.org/10.1021/ar010112aopenalex-snapshot
Transition Metal-Catalyzed Enantioselective Ring-Opening Reactions of Oxabicyclic Alkenes
inferredcites →https://doi.org/10.1021/ar600021zopenalex-snapshot
New Catalytic Reactions of Oxa- and Azabicyclic Alkenes
inferredcites →https://doi.org/10.1021/cr000003uopenalex-snapshot
Synthesis and Reactions of Allylic, Allenic, Vinylic, and Arylmetal Reagents from Halides and Esters via Transient Organopalladium Intermediates
inferredcites →https://doi.org/10.1021/cr1004474openalex-snapshot
Catalytic Enantioselective Allylation of Carbonyl Compounds and Imines
inferredcites →https://doi.org/10.1021/cr9703360openalex-snapshot
Carbon−Carbon Bond Formations Involving Organochromium(III) Reagents
inferredcites →https://doi.org/10.1021/ja00106a062openalex-snapshot
Nickel-Catalyzed Hydroalumination of Oxabicyclic Alkenes. Ligand Effects on the Regio- and Enantioselectivity
inferredcites →https://doi.org/10.1021/ja010498kopenalex-snapshot
Mechanistic Studies of the Palladium-Catalyzed Ring Opening of Oxabicyclic Alkenes with Dialkylzinc
inferredcites →https://doi.org/10.1021/ja204570wopenalex-snapshot
Direct Generation of Acyclic Polypropionate Stereopolyads via Double Diastereo- and Enantioselective Iridium-Catalyzed Crotylation of 1,3-Diols: Beyond Stepwise Carbonyl Addition in Polyketide Construction
inferredcites →https://doi.org/10.1021/ja509077aopenalex-snapshot
Ligand-Controlled Regiodivergent Ni-Catalyzed Reductive Carboxylation of Allyl Esters with CO2
inferredcites →https://doi.org/10.1021/ja802001bopenalex-snapshot
Enantioselective Iridium-Catalyzed Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level Using Allyl Acetate as an Allyl Metal Surrogate
inferredcites →https://doi.org/10.1021/ja805722eopenalex-snapshot
Enantioselective Iridium-Catalyzed Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level via Transfer Hydrogenative Coupling of Allyl Acetate: Departure from Chirally Modified Allyl Metal Reagents in Carbonyl Addition
inferredcites →https://doi.org/10.1021/ja808857wopenalex-snapshot
anti-Diastereo- and Enantioselective Carbonyl Crotylation from the Alcohol or Aldehyde Oxidation Level Employing a Cyclometallated Iridium Catalyst: α-Methyl Allyl Acetate as a Surrogate to Preformed Crotylmetal Reagents
inferredcites →https://doi.org/10.1021/ja971770mopenalex-snapshot
A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes
inferredcites →https://doi.org/10.1021/jacs.0c04735openalex-snapshot
Catalytic Allylation of Aldehydes Using Unactivated Alkenes
inferredcites →https://doi.org/10.1021/jacs.6b01078openalex-snapshot
Hydroxymethylation beyond Carbonylation: Enantioselective Iridium-Catalyzed Reductive Coupling of Formaldehyde with Allylic Acetates via Enantiotopic π-Facial Discrimination
inferredcites →https://doi.org/10.1021/jacs.8b08052openalex-snapshot
Diastereoselective Allylation of Aldehydes by Dual Photoredox and Chromium Catalysis
inferredcites →https://doi.org/10.1021/jo026782ropenalex-snapshot
Iron-Catalyzed Electrochemical Allylation of Carbonyl Compounds by Allylic Acetates
inferredcites →https://doi.org/10.1021/jo061477hopenalex-snapshot
Nickel-Catalyzed Synthesis of Benzocoumarins: Application to the Total Synthesis of Arnottin I
inferredcites →https://doi.org/10.1021/jo200068qopenalex-snapshot
Enhanced anti-Diastereo- and Enantioselectivity in Alcohol-Mediated Carbonyl Crotylation Using an Isolable Single Component Iridium Catalyst
inferredcites →https://doi.org/10.1021/jo902697gopenalex-snapshot
Enantioselective Carbonyl Allylation, Crotylation, and tert-Prenylation of Furan Methanols and Furfurals via Iridium-Catalyzed Transfer Hydrogenation
inferredcites →https://doi.org/10.1039/b615042jopenalex-snapshot
Creation of quaternary stereocenters in carbonyl allylation reactions
inferredcites →https://doi.org/10.1039/c3qo00081hopenalex-snapshot
Catalytic asymmetric allylation of carbonyl compounds and imines with allylic boronates
inferredcites →https://doi.org/10.1039/c7cs00449dopenalex-snapshot
Catalytic nucleophilic ‘umpoled’ π-allyl reagents
inferredcites →https://doi.org/10.1039/c7qo01064hopenalex-snapshot
Cobalt-catalyzed asymmetric reactions of heterobicyclic alkenes with in situ generated organozinc halides
inferredcites →https://doi.org/10.1039/c8ob02864hopenalex-snapshot
Nickel-catalyzed syn -stereocontrolled ring-opening of oxa- and azabicyclic alkenes with dialkylzinc reagents
inferredcites →https://doi.org/10.1039/c8sc05677copenalex-snapshot
Catalytic asymmetric allylation of aldehydes with alkenes through allylic C(sp 3 )–H functionalization mediated by organophotoredox and chiral chromium hybrid catalysis
inferredcites →https://doi.org/10.1039/c9cc03344kopenalex-snapshot
Allylation of aldehydes by dual photoredox and nickel catalysis
inferredcites →https://doi.org/10.1039/d0cs00702aopenalex-snapshot
Catalytic asymmetric transformations of oxa- and azabicyclic alkenes
inferredcites →https://doi.org/10.1039/d1cc06285aopenalex-snapshot
Advances in allylic and benzylic C–H bond functionalization enabled by metallaphotoredox catalysis
inferredcites →https://doi.org/10.1055/s-0040-1705961openalex-snapshot
Nickel-Catalyzed Reductive Allylation of Aldehydes with Allyl Acetates
inferredcites →https://doi.org/10.1055/s-2003-40999openalex-snapshot
Allylation of Carbonyl Compounds by Allylic Acetates Using a Cobalt Halide as Catalyst
inferredcites →https://doi.org/10.1073/pnas.0307271101openalex-snapshot
Rhodium-catalyzed asymmetric ring opening reactions of oxabicyclic alkenes: Catalyst and substrate studies leading to a mechanistic working model
inferredcites →https://doi.org/10.3184/030823408x287104openalex-snapshot
Regio- and stereospecific synthesis of a new benzoconduritol-C derivative

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.4494476openalex-extracted
Rhodium-Catalyzed Ring-Opening Reactions of Azabicyclic Alkenes with Indole Nucleophiles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154685openalex-snapshot
Rhodium-catalyzed ring-opening reactions of heterobicyclic alkenes with heteroarene nucleophiles
inferred← citeshttps://doi.org/10.1016/s1872-2067(26)65016-4openalex-snapshot
Regioselective ring-opening of epoxides triggered by light
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02264openalex-snapshot
Metal-Free Synthesis of Conjugated Dienyl Esters via Coupling of Halopenta-1,4-dienes with Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00017openalex-snapshot
Iridium/Zinc-Co-Catalyzed Ring-Opening Reactions of Oxabicyclic Alkenes with Indole Nucleophiles: A Combined Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01846openalex-snapshot
Nickel-Catalyzed C–N Bond Formation from Ring Remodeling through C–C Bond Activation
inferred← citeshttps://doi.org/10.1021/acscatal.2c03777openalex-snapshot
Rhodium/Amine Dual Catalytic System for Reassembling C≡C Bonds of Conjugated Alkynes with Cyclopropenes via Cutting/Insertion Cascade
inferred← citeshttps://doi.org/10.1021/acscatal.6c01325openalex-snapshot
Single-Site Nickel on Photoactive sp 2 Carbon-Conjugated COF for Synergistic Photocatalytic Organic Transformations
inferred← citeshttps://doi.org/10.1021/jacs.2c09120openalex-snapshot
Investigating Oxidative Addition Mechanisms of Allylic Electrophiles with Low-Valent Ni/Co Catalysts Using Electroanalytical and Data Science Techniques
inferred← citeshttps://doi.org/10.1021/jacs.5c08849openalex-snapshot
Photoredox/Ni-Catalytic Synthesis of cis-Vinyl Iodides from Acetylene
inferred← citeshttps://doi.org/10.1038/s44160-022-00101-9openalex-snapshot
Cooperative triple catalysis enables regioirregular formal Mizoroki–Heck reactions
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