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Electrochemical behavior of N ‐oxyphthalimides: Cascades initiating self‐sustaining catalytic reductive N ― O bond cleavage

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What this work says

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

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Oxidative CO Cross‐Coupling of 1,3‐Dicarbonyl Compounds and Their Heteroanalogues with N‐Substituted Hydroxamic Acids and N‐Hydroxyimides
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Visible‐Light‐Induced Decarboxylative Functionalization of Carboxylic Acids and Their Derivatives
inferredcites →https://doi.org/10.1002/anie.201510014openalex-snapshot
Generation of Alkoxyl Radicals by Photoredox Catalysis Enables Selective C(sp 3 )−H Functionalization under Mild Reaction Conditions
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Combining Traceless Directing Groups with Hybridization Control of Radical Reactivity: From Skipped Enynes to Defect‐Free Hexagonal Frameworks
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Electrochemical Reduction of G3‐Factor Endoperoxide and Its Methyl Ether: Evidence for a Competition between Concerted and Stepwise Dissociative Electron Transfer
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A Radical‐Anion Chain Mechanism Initiated by Dissociative Electron Transfer to a Bicyclic Endoperoxide: Insight into the Fragmentation Chemistry of Neutral Biradicals and Distonic Radical Anions
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Efficient Homogeneous Radical‐Anion Chain Reactions Initiated by Dissociative Electron Transfer to 3,3,6,6‐Tetraaryl‐1,2‐dioxanes
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Approach for the Preparation of Various Classes of Peroxides Based on the Reaction of Triketones with H2O2: First Examples of Ozonide Rearrangements
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Stereoelectronic Chameleons: The Donor–Acceptor Dichotomy of Functional Groups
inferredcites →https://doi.org/10.1002/cmdc.201200225openalex-snapshot
Synthesis and Antimicrobial Activities of Oximes Derived from O‐Benzylhydroxylamine as FabH Inhibitors
inferredcites →https://doi.org/10.1002/jhet.5570370426openalex-snapshot
Synthesis of 1,2‐oxazaheterocycles containing an isoindolone moiety from N‐Hydroxyphthalimide
inferredcites →https://doi.org/10.1002/jlac.197819780916openalex-snapshot
Studien zum Vorgang der Wasserstoffübertragung, 53. Beitrag zur Kenntnis der elektroreduktiven Spaltung von Hydroxylaminderivaten
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Cyclic peroxides as promising anticancer agents: in vitro cytotoxicity study of synthetic ozonides and tetraoxanes on human prostate cancer cell lines
inferredcites →https://doi.org/10.1016/j.bmc.2010.04.074openalex-snapshot
Study of benzo[a]phenazine 7,12-dioxide as selective hypoxic cytotoxin-scaffold. Identification of aerobic-antitumoral activity through DNA fragmentation
inferredcites →https://doi.org/10.1016/j.bmc.2012.03.057openalex-snapshot
Synthesis, biological evaluation, and molecular docking studies of 2,6-dinitro-4-(trifluoromethyl)phenoxysalicylaldoxime derivatives as novel antitubulin agents
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Elucidation of the in vitro and in vivo activities of bridged 1,2,4-trioxolanes, bridged 1,2,4,5-tetraoxanes, tricyclic monoperoxides, silyl peroxides, and hydroxylamine derivatives against Schistosoma mansoni
inferredcites →https://doi.org/10.1016/j.ejmech.2011.01.031openalex-snapshot
Design, synthesis and antifungal activities of novel pyrrole alkaloid analogs
inferredcites →https://doi.org/10.1016/j.jct.2005.07.013openalex-snapshot
Investigations of (acid + base) equilibria in systems modelling interactions occurring in biomolecules
inferredcites →https://doi.org/10.1016/j.jelechem.2014.06.014openalex-snapshot
Electroreduction mechanism of N-arylhydroxylamines in aprotic solvents: N-(4-nitrophenyl)hydroxylamine
inferredcites →https://doi.org/10.1016/j.mencom.2011.01.011openalex-snapshot
Electrochemically initiated transformation of 4-nitrophenylhydroxylamine into 4,4′-dinitroazobenzene
inferredcites →https://doi.org/10.1016/j.saa.2014.06.006openalex-snapshot
Molecular structure, vibrational spectra and 13C and 1H NMR spectral analysis of 1-methylnaphthalene by ab initio HF and DFT methods
inferredcites →https://doi.org/10.1016/j.tet.2012.10.018openalex-snapshot
Generation and cross-coupling of benzyl and phthalimide-N-oxyl radicals in a cerium(IV) ammonium nitrate/N-hydroxyphthalimide/ArCH2R system
inferredcites →https://doi.org/10.1016/s0022-0728(74)80364-5openalex-snapshot
Electrochemical reduction mechanism of phthalimide in DMF
inferredcites →https://doi.org/10.1016/s0040-4020(97)00959-9openalex-snapshot
Development of a new class of rate-accelerating additives for nitroxide-mediated ‘living’ free radical polymerization
inferredcites →https://doi.org/10.1016/s0040-4039(00)60192-2openalex-snapshot
Reductive decarboxylation of N-(acyloxy)phthalimides via redox-initiated radical chain mechanism
inferredcites →https://doi.org/10.1016/s0040-4039(99)01482-3openalex-snapshot
Synthesis of alditols by reductive radical fragmentation of N-phthalimido glycosides. Preparation of chiral synthetic intermediates
inferredcites →https://doi.org/10.1021/acs.jmedchem.6b01164openalex-snapshot
Optimizing Protonation States for Selective Double-Strand DNA Photocleavage in Hypoxic Tumors: pH-Gated Transitions of Lysine Dipeptides
inferredcites →https://doi.org/10.1021/acs.joc.6b01052openalex-snapshot
Domino Fragmentations in Traceless Directing Groups of Radical Cascades: Evidence for the Formation of Alkoxy Radicals via C–O Scission
inferredcites →https://doi.org/10.1021/acs.orglett.5b00570openalex-snapshot
Ruthenium-Catalyzed ortho-C–H Mono- and Di-imidation of Arenes with N-Tosyloxyphthalimide
inferredcites →https://doi.org/10.1021/cr040170kopenalex-snapshot
Free Radical Functionalization of Organic Compounds Catalyzed by N- Hydroxyphthalimide
inferredcites →https://doi.org/10.1021/cr068070xopenalex-snapshot
Electron Transfer Initiated Reactions: Bond Formation and Bond Dissociation
inferredcites →https://doi.org/10.1021/cr940053xopenalex-snapshot
Chemical Redox Agents for Organometallic Chemistry
inferredcites →https://doi.org/10.1021/ja00024a074openalex-snapshot
Photosensitized decarboxylative Michael addition through N-(acyloxy)phthalimides via an electron-transfer mechanism
inferredcites →https://doi.org/10.1021/ja00234a047openalex-snapshot
A new and practical method of decarboxylation: photosensitized decarboxylation of N-acyloxyphthalimides via electron-transfer mechanism
inferredcites →https://doi.org/10.1021/ja00367a028openalex-snapshot
Electron transfer induced reactions. Electrochemically stimulated aromatic nucleophilic substitution in organic solvents
inferredcites →https://doi.org/10.1021/ja00746a029openalex-snapshot
Cathodic reduction of phthalimide systems in nonaqueous solutions
inferredcites →https://doi.org/10.1021/ja066582nopenalex-snapshot
Chiral Photocages Based on Phthalimide Photochemistry
inferredcites →https://doi.org/10.1021/ja510563dopenalex-snapshot
Traceless Directing Groups in Radical Cascades: From Oligoalkynes to Fused Helicenes without Tethered Initiators
inferredcites →https://doi.org/10.1021/ja802123popenalex-snapshot
Carbon−Nitrogen Bond Formation Involving Well-Defined Aryl−Copper(III) Complexes
inferredcites →https://doi.org/10.1021/ja8031218openalex-snapshot
Cu-Facilitated C−O Bond Formation Using N-Hydroxyphthalimide: Efficient and Selective Functionalization of Benzyl and Allylic C−H Bonds
inferredcites →https://doi.org/10.1021/ja9939441openalex-snapshot
Photochemically Removable Protecting Groups Based on Covalently Linked Electron Donor−Acceptor Systems
inferredcites →https://doi.org/10.1021/jm020367+openalex-snapshot
Structure−Activity Relationships of 1,2,4-Benzotriazine 1,4-Dioxides as Hypoxia-Selective Analogues of Tirapazamine
inferredcites →https://doi.org/10.1021/jm101335qopenalex-snapshot
Synthesis and Antiprotozoal Activity of N-Alkoxy Analogues of the Trypanocidal Lead Compound 4,4′-Bis(imidazolinylamino)diphenylamine with Improved Human Blood−Brain Barrier Permeability
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Utilization of Nitrophenylphosphates and Oxime-Based Ligation for the Development of Nanomolar Affinity Inhibitors of the Yersinia pestis Outer Protein H (YopH) Phosphatase
inferredcites →https://doi.org/10.1021/jm3009184openalex-snapshot
Identification of Antischistosomal Leads by Evaluating Bridged 1,2,4,5-Tetraoxanes, Alphaperoxides, and Tricyclic Monoperoxides
inferredcites →https://doi.org/10.1021/jo00025a041openalex-snapshot
Acidity of imidodicarbonates and tosylcarbamates in dimethyl sulfoxide. Correlation with yields in the Mitsunobu reaction
inferredcites →https://doi.org/10.1021/jo00066a014openalex-snapshot
O-Methylarenehydroxamates as ortho-lithiation directing groups. Titanium(III)-mediated conversion of O-methyl hydroxamates to primary amides
inferredcites →https://doi.org/10.1021/jo702364aopenalex-snapshot
Establishment of Heterolytic and Homolytic Y−NO2 Bond Dissociation Energy Scales of Nitro-Containing Compounds in Acetonitrile: Chemical Origin of NO2 Release and Capture
inferredcites →https://doi.org/10.1021/jp810249popenalex-snapshot
Superoxide Protonation by Weak Acids in Imidazolium Based Ionic Liquids
inferredcites →https://doi.org/10.1021/ol202740wopenalex-snapshot
Photoinduced Electron-Transfer-Promoted Redox Fragmentation of N -Alkoxyphthalimides
inferredcites →https://doi.org/10.1021/ol802142kopenalex-snapshot
Chemoselective Oxygen-Centered Radical Cyclizations onto Silyl Enol Ethers
inferredcites →https://doi.org/10.1021/ol990564bopenalex-snapshot
Synthesis of Tetrahydrofurans by a Tandem Hydrogen Atom Abstraction/Radical Nucleophilic Displacement Sequence
inferredcites →https://doi.org/10.1038/nchem.2031openalex-snapshot
The electron is a catalyst
inferredcites →https://doi.org/10.1039/b809356copenalex-snapshot
A radical-anion chain mechanism following dissociative electron transfer reduction of the model prostaglandin endoperoxide, 1,4-diphenyl-2,3-dioxabicyclo[2.2.1]heptane
inferredcites →https://doi.org/10.1039/c2cc36835hopenalex-snapshot
Dissociation of aryl sulfonyl phthalimide radical anions: relevance to the biological activity of aryl sulfonyl amides
inferredcites →https://doi.org/10.1039/c39890001636openalex-snapshot
Photochemical chlorodecarboxylation via an electron transfer mechanism
inferredcites →https://doi.org/10.1039/c3gc41459kopenalex-snapshot
Nitroxide-catalyzed transition-metal-free aerobic oxidation processes
inferredcites →https://doi.org/10.1039/c4cc06344aopenalex-snapshot
Visible-light-induced chemoselective reductive decarboxylative alkynylation under biomolecule-compatible conditions
inferredcites →https://doi.org/10.1039/c6cc06994kopenalex-snapshot
An N-(acetoxy)phthalimide motif as a visible-light pro-photosensitizer in photoredox decarboxylative arylthiation
inferredcites →https://doi.org/10.1039/jr9550003518openalex-snapshot
N-hydroxy-imides. Part II. Derivatives of homophthalic and phthalic acids
inferredcites →https://doi.org/10.1039/p29830000967openalex-snapshot
Reactivity of N-phenacyloxycarbamates and related systems in the presence of bases: study of a new [1,2] anionic rearrangement
inferredcites →https://doi.org/10.1055/s-1998-1711openalex-snapshot
Facile Generation of Alkoxy Radicals from N-Alkoxyphthalimides
inferredcites →https://doi.org/10.1070/rc2012v081n05abeh004244openalex-snapshot
Electrochemically induced chain reactions in organic synthesis
inferredcites →https://doi.org/10.1070/rc2014v83n10abeh004471openalex-snapshot
Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision
inferredcites →https://doi.org/10.1071/ch15356openalex-snapshot
Photodecarboxylative Benzylations of N-Methoxyphthalimide under Batch and Continuous-Flow Conditions
inferredcites →https://doi.org/10.1081/dmr-120005659openalex-snapshot
BIOREDUCTIVELY ACTIVATED ANTITUMORN-OXIDES: THE CASE OF AQ4N, A UNIQUE APPROACH TO HYPOXIA-ACTIVATED CANCER CHEMOTHERAPY
inferredcites →https://doi.org/10.1134/s096554410803002xopenalex-snapshot
Kinetic parameters and geometry of the transition state of decarboxylation reactions of carboxyl and formyl radicals
inferredcites →https://doi.org/10.1139/v81-480openalex-snapshot
The electroreduction of aromatic aldehydes in aprotic solvents
inferredcites →https://doi.org/10.1515/znb-1987-0817openalex-snapshot
Darstellung und Reaktionen von 2-Alkoxy-1,3-bis-(trimethylsilyloxy)-2 H-isoindolen/ Preparation and Reactions of 2-Alkoxy-1,3-bis-(trimethylsilyloxy)-2H-isoindoles
inferredcites →https://doi.org/10.3891/acta.chem.scand.52-0417openalex-snapshot
Electrochemical Reduction of Oximes in Aprotic Media.

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.4670490openalex-extracted
Generation and Radical-Radical Cross-Coupling of Alkenyloxy Radical: Ester and Ketone Synthesis
inferred← citeshttps://doi.org/10.1002/047084289x.rn00598.pub3openalex-snapshot
N ‐Hydroxyphthalimide
inferred← citeshttps://doi.org/10.1002/047084289x.rn02417openalex-snapshot
N ‐Acetoxyphthalimide
inferred← citeshttps://doi.org/10.1002/adsc.201701615openalex-snapshot
N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202000618openalex-snapshot
Electrochemical Synthesis of O‐Phthalimide Oximes from α‐Azido Styrenes via Radical Sequence: Generation, Addition and Recombination of Imide‐N‐Oxyl and Iminyl Radicals with C−O/N−O Bonds Formation
inferred← citeshttps://doi.org/10.1002/adsc.70035openalex-snapshot
Harnessing Vinylogy with Radicals: Photoinduced γ‐Benzylation Reactions of 2‐Silyloxyfurans
inferred← citeshttps://doi.org/10.1002/ajoc.202200262openalex-snapshot
N‐Alkoxyphtalimides as Versatile Alkoxy Radical Precursors in Modern Organic Synthesis
inferred← citeshttps://doi.org/10.1002/ajoc.202300160openalex-snapshot
Alkoxy Radical Induced Transformations from N‐Alkoxyphthalimides Under the Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/ajoc.202400503openalex-snapshot
N‐Oxyl Radicals in Oxidative C−O Coupling: Free‐Radical Hydrogen Substitution and Addition to C=C Bonds
inferred← citeshttps://doi.org/10.1002/ange.201807247openalex-snapshot
Hochkonversion von Reduktionsmitteln
inferred← citeshttps://doi.org/10.1002/anie.201807247openalex-snapshot
Upconversion of Reductants
inferred← citeshttps://doi.org/10.1002/cctc.202300489openalex-snapshot
N‐(aminobenzyliden)phthalimides as a New Redox Mediator Family for the Selective Indirect Reduction of Benzyl or Allyl Halides
inferred← citeshttps://doi.org/10.1002/cssc.202501605openalex-snapshot
Electrochemical and Photoredox Catalysis for Constructing 5,5‐Spirocycles via Reductive Activation of N ‐alkoxyphthalimides for the Total Synthesis of (−)‐Cephalosporolide F
inferred← citeshttps://doi.org/10.1002/tcr.202100056openalex-snapshot
Electrochemical Generation and Use in Organic Synthesis of C ‐, O ‐, and N ‐Centered Radicals
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N-(Alkoxy)- and N-(acyloxy)phthalimides in organic synthesis: free radical synthetic approaches and applications (microreview)
inferred← citeshttps://doi.org/10.1007/s11172-022-3570-7openalex-snapshot
Electron upconversion in reactions of 1,2,4-triazoline-3,5-dione
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Electrochemically induced decomposition of benzopinacol
inferred← citeshttps://doi.org/10.1016/j.crgsc.2024.100404openalex-snapshot
Highly efficient electrogeneration of oxygen centered radicals from N-alkoxyphthalimides employing rapid alternating polarity (RAP) electrolysis. Transferring the photoredox catalytic conditions to organic electrosynthesis
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e23808openalex-snapshot
Access to carbonyl compounds via the electroreduction of N-benzyloxyphthalimides: Mechanism confirmation and preparative applications
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155367openalex-snapshot
Electricity-driven reductive coupling reaction of imines with N-(acyloxy)phthalimides
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00278openalex-snapshot
Generation of Alkyl Radicals: From the Tyranny of Tin to the Photon Democracy
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00977openalex-snapshot
Organo Photoinduced Decarboxylative Alkylation of Coumarins with N-(Acyloxy)phthalimide
inferred← citeshttps://doi.org/10.1021/acs.jpcc.4c00538openalex-snapshot
Redox Upconversion and Electrocatalytic Cycles in Activation of Si–Si Bonds: Diverging Reactivity in Hole- and Electron-Catalyzed Transformations
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00443openalex-snapshot
Copper or Silver-Mediated Oxidative C(sp2)–H/N–H Cross-Coupling of Phthalimide and Heterocyclic Arenes: Access to N-Arylphthalimides
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01552openalex-snapshot
Electrochemical Deconstructive Functionalization of Cycloalkanols via Alkoxy Radicals Enabled by Proton-Coupled Electron Transfer
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00627openalex-snapshot
Generation and Radical–Radical Cross-Coupling of Alkenyloxy Radical
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01547openalex-snapshot
A Dual Ni/Photoredox Cross-Coupling Approach toward Mandelic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03524openalex-snapshot
Site-Tunable Csp3–H Bonds Functionalization by Visible-Light-Induced Radical Translocation of N-Alkoxyphthalimides
inferred← citeshttps://doi.org/10.1021/acsinfocus.7e7009openalex-snapshot
Oxygen: The Key to Stereoelectronic Control in Chemistry
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inferred← citeshttps://doi.org/10.1021/jacs.4c10422openalex-snapshot
The Photoredox Paradox: Electron and Hole Upconversion as the Hidden Secrets of Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.5c17610openalex-snapshot
Reactions of Radical Anions with Hydrides: Supercharging Electron Upconversion for Electron Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.7b07519openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41467-020-18275-1openalex-snapshot
Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy
inferred← citeshttps://doi.org/10.1038/s41467-021-27165-zopenalex-snapshot
A general strategy for C(sp3)–H functionalization with nucleophiles using methyl radical as a hydrogen atom abstractor
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inferred← citeshttps://doi.org/10.1038/s41929-023-01073-5openalex-snapshot
Interfacial tuning of electrocatalytic Ag surfaces for fragment-based electrophile coupling
inferred← citeshttps://doi.org/10.1039/c9cc00035fopenalex-snapshot
Alkoxy radicals generation: facile photocatalytic reduction of N -alkoxyazinium or azolium salts
inferred← citeshttps://doi.org/10.1039/c9cc09973eopenalex-snapshot
High-efficiency cathodic electrochemiluminescence of the tris(2,2′-bipyridine)ruthenium( ii )/ N -hydroxy compound system and its use for sensitive “turn-on” detection of mercury( ii ) and methyl blue
inferred← citeshttps://doi.org/10.1039/c9sc04846dopenalex-snapshot
Chain propagation determines the chemo- and regioselectivity of alkyl radical additions to C–O vs. C–C double bonds
inferred← citeshttps://doi.org/10.1039/d1ob00420dopenalex-snapshot
Recent progress on electrochemical synthesis involving carboxylic acids
inferred← citeshttps://doi.org/10.1039/d2cc06999gopenalex-snapshot
Electrochemical C(sp 3 )–H functionalization of ethers via hydrogen-atom transfer by means of cathodic reduction
inferred← citeshttps://doi.org/10.1039/d2sc01342hopenalex-snapshot
Catalytic electron drives host–guest recognition
inferred← citeshttps://doi.org/10.1039/d3cc00302gopenalex-snapshot
Electrochemical generation and utilization of alkoxy radicals
inferred← citeshttps://doi.org/10.1039/d5qo00991jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1055/a-1467-5585openalex-snapshot
Tetrabutylammonium Iodide (TBAI) Catalyzed Electrochemical C–H Bond Activation of 2-Arylated N-Methoxyamides for the Synthesis of Phenanthridinones
inferred← citeshttps://doi.org/10.1055/a-2916-2299openalex-snapshot
From Organotin-Based Reactions to Photoredox and Electrochemical Processes: The Journey of Alkoxy Radicals in the Total Syntheses of Cephalosporolides E and F
inferred← citeshttps://doi.org/10.1070/rcr5022openalex-snapshot
Transition metal-free cross-coupling reactions to form carbon–heteroatom bonds
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Reactivity of Radical Anions and Dianions of Organic Compounds: A Review
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Electrogeneration of O-centered Radicals from N-alkoxyphthalimides and their use in δ-C-H functionalization. Comparison with the Photocatalytic Redox reaction
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REACTIVITY OF ANION RADICAL AND DIANION OF ORGANIC COMPOUNDS (REVIEW)
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A Second Job for Electron Upconversion: Single-Electron Activation of Leaving-Group Departure
inferred← citeshttps://doi.org/10.5796/electrochemistry.23-67079openalex-snapshot
Cathodic N–O Bond Cleavage of N-Alkoxy Amide
inferred← citeshttps://doi.org/10.70675/212be2e3z395bz44a8zaf33z0f6b32488780openalex-snapshot
Modification chimique de polymères par des dérivés acyloxyimides en extrusion réactive
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