VIAF

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Leader     00000nz a2200037n 45 0
001     WKP|Q41910362  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241221010719.0
008     241221nneanz||abbn n and d
035 ‎‡a  (WKP)Q41910362‏
024 ‎‡a  0000-0003-3136-0845‏ ‎‡2  orcid‏
024 ‎‡a  7404113131‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q41910362‏
100 0 ‎‡a  John A Murphy‏ ‎‡9  es‏ ‎‡9  sl‏ ‎‡9  ast‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  জন এ মার্ফি‏ ‎‡c  গবেষক‏ ‎‡9  bn‏
400 0 ‎‡a  John A Murphy‏ ‎‡c  researcher‏ ‎‡9  en‏
400 0 ‎‡a  John A Murphy‏ ‎‡c  onderzoeker‏ ‎‡9  nl‏
670 ‎‡a  Author's 1,4-pentadienyl-3-sulfonamides: frameworks for "disfavored" radical cascade cyclizations‏
670 ‎‡a  Author's A construction of 4,4-spirocyclic γ-lactams by tandem radical cyclization with carbon monoxide‏
670 ‎‡a  Author's A Powerful Palladium-Catalyzed Multicomponent Process for the Preparation of Oxazolines and Benzoxazoles‏
670 ‎‡a  Author's A study of diketopiperazines as electron-donor initiators in transition metal-free haloarene-arene coupling‏
670 ‎‡a  Author's Amination of arenes through electron-deficient reaction cascades of aryl epoxyazides‏
670 ‎‡a  Author's Applications of organocatalysed visible-light photoredox reactions for medicinal chemistry‏
670 ‎‡a  Author's Concerted Nucleophilic Aromatic Substitution Reactions‏
670 ‎‡a  Author's Concise synthesis of (+/-)-horsfiline and (+/-)-coerulescine by tandem cyclisation of iodoaryl alkenyl azides‏
670 ‎‡a  Author's Contra-thermodynamic Hydrogen Atom Abstraction in the Selective C-H Functionalization of Trialkylamine N-CH3 Groups‏
670 ‎‡a  Author's Diethylphosphine oxide‏
670 ‎‡a  Author's Diethylphosphine oxide (DEPO): high-yielding and facile preparation of indolones in water‏
670 ‎‡a  Author's Discovery and development of organic super-electron-donors‏
670 ‎‡a  Author's Discovery of the first potent and selective αvβ5 integrin inhibitor based on an amide-containing core‏
670 ‎‡a  Author's Double Deprotonation of Pyridinols Generates Potent Organic Electron-Donor Initiators for Haloarene-Arene Coupling‏
670 ‎‡a  Author's Dual Roles for Potassium Hydride in Haloarene Reduction: CSNAr and Single Electron Transfer Reduction via Organic Electron Donors Formed in Benzene‏
670 ‎‡a  Author's Effect of solvent on radical cyclisation pathways: SRN1 vs. aryl-aryl bond forming mechanisms‏
670 ‎‡a  Author's Electron-Transfer and Hydride-Transfer Pathways in the Stoltz-Grubbs Reducing System‏
670 ‎‡a  Author's Electron-Transfer and Hydride-Transfer Pathways in the Stoltz-Grubbs Reducing System (KOtBu/Et3 SiH).‏
670 ‎‡a  Author's Electron transfer-induced coupling of haloarenes to styrenes and 1,1-diphenylethenes triggered by diketopiperazines and Potassium tert-butoxide‏
670 ‎‡a  Author's Electron Transfer Reactions: KOtBu‏
670 ‎‡a  Author's Electron Transfer Reactions: KOtBu (but not NaOtBu) Photoreduces Benzophenone under Activation by Visible Light‏
670 ‎‡a  Author's Evidence of single electron transfer from the enolate anion of an N,N'-dialkyldiketopiperazine additive in BHAS coupling reactions‏
670 ‎‡a  Author's Evolution in the understanding of [Fe]-hydrogenase.‏
670 ‎‡a  Author's Evolution of neutral organic super-electron-donors and their applications‏
670 ‎‡a  Author's Formal total synthesis of (+/-)-vindoline by tandem radical cyclization‏
670 ‎‡a  Author's Fragmentation of nitrone triflates to 9-membered rings‏
670 ‎‡a  Author's Fragmentations observed in the reactions of α-methoxy-γ-alkoxyalkyl iodide substrates with super-electron-donors derived from 4-DMAP and N-methylbenzimidazole‏
670 ‎‡a  Author's Highly efficient reduction of unactivated aryl and alkyl iodides by a ground-state neutral organic electron donor‏
670 ‎‡a  Author's Homoleptic crown N-heterocyclic carbene complexes‏
670 ‎‡a  Author's Hybrid super electron donors - preparation and reactivity‏
670 ‎‡a  Author's Hydrogen Atom Transfer-Mediated Cyclisations of Nitriles‏
670 ‎‡a  Author's Hydrogen Atom Transfer-Mediated Domino Cyclisation Reaction to Access (Spiro)Quinazolinones‏
670 ‎‡a  Author's Identifying the Roles of Amino Acids, Alcohols and 1,2-Diamines as Mediators in Coupling of Haloarenes to Arenes‏
670 ‎‡a  Author's KOBu as a Single Electron Donor? Revisiting the Halogenation of Alkanes with CBr₄ and CCl₄‏
670 ‎‡a  Author's KOtBu: A Privileged Reagent for Electron Transfer Reactions?‏
670 ‎‡a  Author's M4 agonists/5HT7 antagonists with potential as antischizophrenic drugs: serominic compounds‏
670 ‎‡a  Author's Mechanistic Exploration of the Palladium-catalyzed Process for the Synthesis of Benzoxazoles and Benzothiazoles‏
670 ‎‡a  Author's Metal-free reductive cleavage of benzylic esters and ethers: fragmentations result from single and double electron transfers.‏
670 ‎‡a  Author's Metal-free reductive cleavage of C-N and S-N bonds by photoactivated electron transfer from a neutral organic donor‏
670 ‎‡a  Author's Neutral Organic Super Electron Donors Made Catalytic‏
670 ‎‡a  Author's One-carbon extrusion from a tetraazafulvalene. Isolation of aldehydes and a study of their origin‏
670 ‎‡a  Author's One-pot functionalisation of N-substituted tetrahydroisoquinolines by photooxidation and tunable organometallic trapping of iminium intermediates‏
670 ‎‡a  Author's Overturning established chemoselectivities: selective reduction of arenes over malonates and cyanoacetates by photoactivated organic electron donors‏
670 ‎‡a  Author's Physical organic chemistry‏
670 ‎‡a  Author's Pushing the limits of neutral organic electron donors: a tetra(iminophosphorano)-substituted bispyridinylidene.‏
670 ‎‡a  Author's Reactions of triflate esters and triflamides with an organic neutral super-electron-donor.‏
670 ‎‡a  Author's Reduction of arenediazonium salts by tetrakis‏
670 ‎‡a  Author's Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): efficient formation of products derived from aryl radicals‏
670 ‎‡a  Author's Reductions of challenging organic substrates by a nickel complex of a noninnocent crown carbene ligand‏
670 ‎‡a  Author's Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor‏
670 ‎‡a  Author's Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor (S.E.D.) reagent.‏
670 ‎‡a  Author's Selectively Targeting the Kinome-Conserved Lysine of PI3Kδ as a General Approach to Covalent Kinase Inhibition‏
670 ‎‡a  Author's Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine.‏
670 ‎‡a  Author's Super-electron donors: bis-pyridinylidene formation by base treatment of pyridinium salts.‏
670 ‎‡a  Author's Superelectrophilic Amidine Dications: Dealkylation by Triflate Anion‏
670 ‎‡a  Author's The generation of aryl anions by double electron transfer to aryl iodides from a neutral ground-state organic super-electron donor.‏
670 ‎‡a  Author's Visible light-mediated Smiles rearrangements and annulations of non-activated aromatics‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/processed/DNB|1029931143‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/viaf/295253946‏
909 ‎‡a  (orcid) 0000000331360845‏ ‎‡9  1‏
909 ‎‡a  (scopus) 7404113131‏ ‎‡9  1‏
919 ‎‡a  1carbonextrusionfromatetraazafulvaleneisolationofaldehydesandastudyoftheirorigin‏ ‎‡A  One-carbon extrusion from a tetraazafulvalene. Isolation of aldehydes and a study of their origin‏ ‎‡9  1‏
919 ‎‡a  1potfunctionalisationofnsubstitutedtetrahydroisoquinolinesbyphotooxidationandtunableorganometallictrappingofiminiumintermediates‏ ‎‡A  One-pot functionalisation of N-substituted tetrahydroisoquinolines by photooxidation and tunable organometallic trapping of iminium intermediates‏ ‎‡9  1‏
919 ‎‡a  overturningestablishedchemoselectivitiesselectivereductionofarenesovermalonatesandcyanoacetatesbyphotoactivatedorganicelectrondonors‏ ‎‡A  Overturning established chemoselectivities: selective reduction of arenes over malonates and cyanoacetates by photoactivated organic electron donors‏ ‎‡9  1‏
919 ‎‡a  physicalorganicchemistry‏ ‎‡A  Physical organic chemistry‏ ‎‡9  1‏
919 ‎‡a  pushingthelimitsofneutralorganicelectrondonorsatetraiminophosphoranosubstitutedbispyridinylidene‏ ‎‡A  Pushing the limits of neutral organic electron donors: a tetra(iminophosphorano)-substituted bispyridinylidene.‏ ‎‡9  1‏
919 ‎‡a  reactionsoftriflateestersandtriflamideswithanorganicneutralsuperelectrondonor‏ ‎‡A  Reactions of triflate esters and triflamides with an organic neutral super-electron-donor.‏ ‎‡9  1‏
919 ‎‡a  reductionofarenediazoniumsaltsbytetrakis‏ ‎‡A  Reduction of arenediazonium salts by tetrakis‏ ‎‡9  1‏
919 ‎‡a  reductionofarenediazoniumsaltsbytetrakisdimethylaminoethylenetdaeefficientformationofproductsderivedfromarylradicals‏ ‎‡A  Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): efficient formation of products derived from aryl radicals‏ ‎‡9  1‏
919 ‎‡a  reductionsofchallengingorganicsubstratesbyanickelcomplexofanoninnocentcrowncarbeneligand‏ ‎‡A  Reductions of challenging organic substrates by a nickel complex of a noninnocent crown carbene ligand‏ ‎‡9  1‏
919 ‎‡a  visiblelightmediatedsmilesrearrangementsandannulationsofnonactivatedaromatics‏ ‎‡A  Visible light-mediated Smiles rearrangements and annulations of non-activated aromatics‏ ‎‡9  1‏
919 ‎‡a  generationofarylanionsbydoubleelectrontransfertoaryliodidesfromaneutralgroundstateorganicsuperelectrondonor‏ ‎‡A  The generation of aryl anions by double electron transfer to aryl iodides from a neutral ground-state organic super-electron donor.‏ ‎‡9  1‏
919 ‎‡a  reductivecleavageofsulfonesandsulfonamidesbyaneutralorganicsuperelectrondonor‏ ‎‡A  Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor‏ ‎‡9  1‏
919 ‎‡a  reductivecleavageofsulfonesandsulfonamidesbyaneutralorganicsuperelectrondonorse500reagent‏ ‎‡A  Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor (S.E.D.) reagent.‏ ‎‡9  1‏
919 ‎‡a  superelectrophilicamidinedicationsdealkylationbytriflateanion‏ ‎‡A  Superelectrophilic Amidine Dications: Dealkylation by Triflate Anion‏ ‎‡9  1‏
919 ‎‡a  superelectrondonorsbispyridinylideneformationbybasetreatmentofpyridiniumsalts‏ ‎‡A  Super-electron donors: bis-pyridinylidene formation by base treatment of pyridinium salts.‏ ‎‡9  1‏
919 ‎‡a  structureandreactivityinneutralorganicelectrondonorsderivedfrom4dimethylaminopyridine‏ ‎‡A  Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine.‏ ‎‡9  1‏
919 ‎‡a  selectivelytargetingthekinomeconservedlysineofpi3kδasageneralapproachtocovalentkinaseinhibition‏ ‎‡A  Selectively Targeting the Kinome-Conserved Lysine of PI3Kδ as a General Approach to Covalent Kinase Inhibition‏ ‎‡9  1‏
919 ‎‡a  14pentadienyl3sulfonamidesframeworksfordisfavoredradicalcascadecyclizations‏ ‎‡A  1,4-pentadienyl-3-sulfonamides: frameworks for "disfavored" radical cascade cyclizations‏ ‎‡9  1‏
919 ‎‡a  constructionof44spirocyclicγlactamsbytandemradicalcyclizationwithcarbonmonoxide‏ ‎‡A  A construction of 4,4-spirocyclic γ-lactams by tandem radical cyclization with carbon monoxide‏ ‎‡9  1‏
919 ‎‡a  powerfulpalladiumcatalyzedmulticomponentprocessforthepreparationofoxazolinesandbenzoxazoles‏ ‎‡A  A Powerful Palladium-Catalyzed Multicomponent Process for the Preparation of Oxazolines and Benzoxazoles‏ ‎‡9  1‏
919 ‎‡a  studyofdiketopiperazinesaselectrondonorinitiatorsintransitionmetalfreehaloarenearenecoupling‏ ‎‡A  A study of diketopiperazines as electron-donor initiators in transition metal-free haloarene-arene coupling‏ ‎‡9  1‏
919 ‎‡a  aminationofarenesthroughelectrondeficientreactioncascadesofarylepoxyazides‏ ‎‡A  Amination of arenes through electron-deficient reaction cascades of aryl epoxyazides‏ ‎‡9  1‏
919 ‎‡a  applicationsoforganocatalysedvisiblelightphotoredoxreactionsformedicinalchemistry‏ ‎‡A  Applications of organocatalysed visible-light photoredox reactions for medicinal chemistry‏ ‎‡9  1‏
919 ‎‡a  concertednucleophilicaromaticsubstitutionreactions‏ ‎‡A  Concerted Nucleophilic Aromatic Substitution Reactions‏ ‎‡9  1‏
919 ‎‡a  concisesynthesisof+horsfilineand+coerulescinebytandemcyclisationofiodoarylalkenylazides‏ ‎‡A  Concise synthesis of (+/-)-horsfiline and (+/-)-coerulescine by tandem cyclisation of iodoaryl alkenyl azides‏ ‎‡9  1‏
919 ‎‡a  contrathermodynamichydrogenatomabstractionintheselective100hfunctionalizationoftrialkylaminench3groups‏ ‎‡A  Contra-thermodynamic Hydrogen Atom Abstraction in the Selective C-H Functionalization of Trialkylamine N-CH3 Groups‏ ‎‡9  1‏
919 ‎‡a  diethylphosphineoxide‏ ‎‡A  Diethylphosphine oxide‏ ‎‡9  1‏
919 ‎‡a  diethylphosphineoxidedepohighyieldingandfacilepreparationofindolonesinwater‏ ‎‡A  Diethylphosphine oxide (DEPO): high-yielding and facile preparation of indolones in water‏ ‎‡9  1‏
919 ‎‡a  discoveryanddevelopmentoforganicsuperelectrondonors‏ ‎‡A  Discovery and development of organic super-electron-donors‏ ‎‡9  1‏
919 ‎‡a  discoveryofthe1potentandselectiveαvβ5integrininhibitorbasedonanamidecontainingcore‏ ‎‡A  Discovery of the first potent and selective αvβ5 integrin inhibitor based on an amide-containing core‏ ‎‡9  1‏
919 ‎‡a  doubledeprotonationofpyridinolsgeneratespotentorganicelectrondonorinitiatorsforhaloarenearenecoupling‏ ‎‡A  Double Deprotonation of Pyridinols Generates Potent Organic Electron-Donor Initiators for Haloarene-Arene Coupling‏ ‎‡9  1‏
919 ‎‡a  dualrolesforpotassiumhydrideinhaloarenereductioncsnarandsingleelectrontransferreductionviaorganicelectrondonorsformedinbenzene‏ ‎‡A  Dual Roles for Potassium Hydride in Haloarene Reduction: CSNAr and Single Electron Transfer Reduction via Organic Electron Donors Formed in Benzene‏ ‎‡9  1‏
919 ‎‡a  effectofsolventonradicalcyclisationpathwayssrn1vsarylarylbondformingmechanisms‏ ‎‡A  Effect of solvent on radical cyclisation pathways: SRN1 vs. aryl-aryl bond forming mechanisms‏ ‎‡9  1‏
919 ‎‡a  electrontransferandhydridetransferpathwaysinthestoltzgrubbsreducingsystem‏ ‎‡A  Electron-Transfer and Hydride-Transfer Pathways in the Stoltz-Grubbs Reducing System‏ ‎‡9  1‏
919 ‎‡a  electrontransferandhydridetransferpathwaysinthestoltzgrubbsreducingsystemkotbuet3sih‏ ‎‡A  Electron-Transfer and Hydride-Transfer Pathways in the Stoltz-Grubbs Reducing System (KOtBu/Et3 SiH).‏ ‎‡9  1‏
919 ‎‡a  electrontransferinducedcouplingofhaloarenestostyrenesand11diphenylethenestriggeredbydiketopiperazinesandpotassiumtertbutoxide‏ ‎‡A  Electron transfer-induced coupling of haloarenes to styrenes and 1,1-diphenylethenes triggered by diketopiperazines and Potassium tert-butoxide‏ ‎‡9  1‏
919 ‎‡a  electrontransferreactionskotbu‏ ‎‡A  Electron Transfer Reactions: KOtBu‏ ‎‡9  1‏
919 ‎‡a  electrontransferreactionskotbubutnotnaotbuphotoreducesbenzophenoneunderactivationbyvisiblelight‏ ‎‡A  Electron Transfer Reactions: KOtBu (but not NaOtBu) Photoreduces Benzophenone under Activation by Visible Light‏ ‎‡9  1‏
919 ‎‡a  evidenceofsingleelectrontransferfromtheenolateanionofannndialkyldiketopiperazineadditiveinbhascouplingreactions‏ ‎‡A  Evidence of single electron transfer from the enolate anion of an N,N'-dialkyldiketopiperazine additive in BHAS coupling reactions‏ ‎‡9  1‏
919 ‎‡a  evolutionintheunderstandingofhydrogenase‏ ‎‡A  Evolution in the understanding of [Fe]-hydrogenase.‏ ‎‡9  1‏
919 ‎‡a  evolutionofneutralorganicsuperelectrondonorsandtheirapplications‏ ‎‡A  Evolution of neutral organic super-electron-donors and their applications‏ ‎‡9  1‏
919 ‎‡a  formaltotalsynthesisof+vindolinebytandemradicalcyclization‏ ‎‡A  Formal total synthesis of (+/-)-vindoline by tandem radical cyclization‏ ‎‡9  1‏
919 ‎‡a  fragmentationofnitronetriflatesto9memberedrings‏ ‎‡A  Fragmentation of nitrone triflates to 9-membered rings‏ ‎‡9  1‏
919 ‎‡a  fragmentationsobservedinthereactionsofαmethoxyγalkoxyalkyliodidesubstrateswithsuperelectrondonorsderivedfrom4dmapandnmethylbenzimidazole‏ ‎‡A  Fragmentations observed in the reactions of α-methoxy-γ-alkoxyalkyl iodide substrates with super-electron-donors derived from 4-DMAP and N-methylbenzimidazole‏ ‎‡9  1‏
919 ‎‡a  highlyefficientreductionofunactivatedarylandalkyliodidesbyagroundstateneutralorganicelectrondonor‏ ‎‡A  Highly efficient reduction of unactivated aryl and alkyl iodides by a ground-state neutral organic electron donor‏ ‎‡9  1‏
919 ‎‡a  homolepticcrownnheterocycliccarbenecomplexes‏ ‎‡A  Homoleptic crown N-heterocyclic carbene complexes‏ ‎‡9  1‏
919 ‎‡a  hybridsuperelectrondonorspreparationandreactivity‏ ‎‡A  Hybrid super electron donors - preparation and reactivity‏ ‎‡9  1‏
919 ‎‡a  hydrogenatomtransfermediatedcyclisationsofnitriles‏ ‎‡A  Hydrogen Atom Transfer-Mediated Cyclisations of Nitriles‏ ‎‡9  1‏
919 ‎‡a  hydrogenatomtransfermediateddominocyclisationreactiontoaccessspiroquinazolinones‏ ‎‡A  Hydrogen Atom Transfer-Mediated Domino Cyclisation Reaction to Access (Spiro)Quinazolinones‏ ‎‡9  1‏
919 ‎‡a  identifyingtherolesofaminoacidsalcoholsand12diaminesasmediatorsincouplingofhaloarenestoarenes‏ ‎‡A  Identifying the Roles of Amino Acids, Alcohols and 1,2-Diamines as Mediators in Coupling of Haloarenes to Arenes‏ ‎‡9  1‏
919 ‎‡a  kobuasasingleelectrondonorrevisitingthehalogenationofalkaneswithcbr4andccl4‏ ‎‡A  KOBu as a Single Electron Donor? Revisiting the Halogenation of Alkanes with CBr₄ and CCl₄‏ ‎‡9  1‏
919 ‎‡a  kotbuaprivilegedreagentforelectrontransferreactions‏ ‎‡A  KOtBu: A Privileged Reagent for Electron Transfer Reactions?‏ ‎‡9  1‏
919 ‎‡a  m4agonists5ht7antagonistswithpotentialasantischizophrenicdrugsserominiccompounds‏ ‎‡A  M4 agonists/5HT7 antagonists with potential as antischizophrenic drugs: serominic compounds‏ ‎‡9  1‏
919 ‎‡a  mechanisticexplorationofthepalladiumcatalyzedprocessforthesynthesisofbenzoxazolesandbenzothiazoles‏ ‎‡A  Mechanistic Exploration of the Palladium-catalyzed Process for the Synthesis of Benzoxazoles and Benzothiazoles‏ ‎‡9  1‏
919 ‎‡a  metalfreereductivecleavageofbenzylicestersandethersfragmentationsresultfromsingleanddoubleelectrontransfers‏ ‎‡A  Metal-free reductive cleavage of benzylic esters and ethers: fragmentations result from single and double electron transfers.‏ ‎‡9  1‏
919 ‎‡a  metalfreereductivecleavageof100nandsnbondsbyphotoactivatedelectrontransferfromaneutralorganicdonor‏ ‎‡A  Metal-free reductive cleavage of C-N and S-N bonds by photoactivated electron transfer from a neutral organic donor‏ ‎‡9  1‏
919 ‎‡a  neutralorganicsuperelectrondonorsmadecatalytic‏ ‎‡A  Neutral Organic Super Electron Donors Made Catalytic‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
996 ‎‡2  BAV|495_232933‏
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996 ‎‡2  NUKAT|n 2006044543‏
996 ‎‡2  BNF|14123687‏
996 ‎‡2  NII|DA04267625‏
996 ‎‡2  SUDOC|273379135‏
996 ‎‡2  LC|no2022149747‏
996 ‎‡2  NII|DA19515298‏
996 ‎‡2  LC|n 2016002008‏
996 ‎‡2  LC|nb2010003103‏
996 ‎‡2  J9U|987007359932705171‏
996 ‎‡2  RERO|A006187486‏
996 ‎‡2  N6I|vtls000083069‏
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996 ‎‡2  LC|no2010135388‏
996 ‎‡2  DNB|135161858X‏
996 ‎‡2  ISNI|000000004637907X‏
996 ‎‡2  LC|no2024066620‏
996 ‎‡2  LC|n 97900116‏
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996 ‎‡2  NUKAT|n 2010130952‏
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996 ‎‡2  CAOONL|ncf10242423‏
996 ‎‡2  LC|n 2011030813‏
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996 ‎‡2  LC|n 90000280‏
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996 ‎‡2  ISNI|0000000045729242‏
996 ‎‡2  LC|no2007135677‏
996 ‎‡2  NLA|000035076917‏
996 ‎‡2  BNF|11930511‏
996 ‎‡2  LIH|LNB:C_p__f_,;=B0‏
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996 ‎‡2  N6I|vtls002050180‏
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996 ‎‡2  BNF|15063998‏
996 ‎‡2  ISNI|0000000063986461‏
996 ‎‡2  DNB|1282101382‏
996 ‎‡2  BNE|XX866152‏
996 ‎‡2  ISNI|0000000101922304‏
996 ‎‡2  DNB|1099993946‏
996 ‎‡2  BNF|12375581‏
996 ‎‡2  DNB|1265151571‏
996 ‎‡2  SIMACOB|139890019‏
996 ‎‡2  DNB|131229048X‏
996 ‎‡2  DNB|1174840951‏
996 ‎‡2  LC|n 2012002641‏
996 ‎‡2  LC|nb2010003100‏
996 ‎‡2  DNB|1201323800‏
996 ‎‡2  LC|n 00027942‏
996 ‎‡2  N6I|vtls002795136‏
996 ‎‡2  LC|n 91044395‏
996 ‎‡2  DBC|87097969618677‏
996 ‎‡2  J9U|987009541110805171‏
996 ‎‡2  DBC|87097968733634‏
996 ‎‡2  CAOONL|ncf11369698‏
996 ‎‡2  LC|n 2018061879‏
996 ‎‡2  NKC|vse20241224711‏
996 ‎‡2  ISNI|0000000109532300‏
996 ‎‡2  LC|no2016110477‏
996 ‎‡2  NUKAT|n 2008141624‏
996 ‎‡2  SUDOC|233178503‏
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996 ‎‡2  LC|nb2001021957‏
996 ‎‡2  LC|no 93031273‏
996 ‎‡2  ISNI|0000000039126664‏
996 ‎‡2  LC|n 83319250‏
996 ‎‡2  DNB|136721710‏
996 ‎‡2  NLA|000067599477‏
996 ‎‡2  NUKAT|n 2015143640‏
996 ‎‡2  RERO|A027230492‏
996 ‎‡2  J9U|987012330224405171‏
996 ‎‡2  J9U|987007430173005171‏
996 ‎‡2  BIBSYS|14062981‏
996 ‎‡2  ISNI|0000000067049715‏
996 ‎‡2  NTA|307936783‏
996 ‎‡2  ISNI|0000000119382537‏
996 ‎‡2  LC|n 95072957‏
996 ‎‡2  NUKAT|n 2019070215‏
996 ‎‡2  LC|n 95071221‏
996 ‎‡2  ISNI|0000000054697633‏
996 ‎‡2  DNB|1217816003‏
996 ‎‡2  BIBSYS|1678650010668‏
996 ‎‡2  LC|n 94802955‏
996 ‎‡2  ISNI|000000006498074X‏
996 ‎‡2  CAOONL|ncf10329890‏
996 ‎‡2  SUDOC|140164766‏
996 ‎‡2  RERO|A003619697‏
996 ‎‡2  RERO|A003619696‏
996 ‎‡2  ISNI|0000000064035908‏
996 ‎‡2  DBC|87097968733626‏
996 ‎‡2  ISNI|0000000052748820‏
996 ‎‡2  ISNI|0000000067139075‏
996 ‎‡2  DNB|1139005383‏
996 ‎‡2  NII|DA07199270‏
996 ‎‡2  BIBSYS|9058628‏
996 ‎‡2  J9U|987007392050805171‏
996 ‎‡2  ISNI|0000000083856672‏
996 ‎‡2  LC|nb 90231034‏
996 ‎‡2  CAOONL|ncf12058961‏
996 ‎‡2  ISNI|0000000034527290‏
996 ‎‡2  NUKAT|n 96033646‏
996 ‎‡2  LC|n 2014019896‏
996 ‎‡2  LC|nb 98004384‏
996 ‎‡2  N6I|vtls001122067‏
996 ‎‡2  LC|n 2001029628‏
996 ‎‡2  LC|n 2005051666‏
996 ‎‡2  N6I|vtls000323726‏
996 ‎‡2  LC|n 88035761‏
996 ‎‡2  J9U|987007459330405171‏
996 ‎‡2  NUKAT|n 2011072433‏
996 ‎‡2  ISNI|0000000084412491‏
996 ‎‡2  NTA|071676449‏
996 ‎‡2  SUDOC|157866947‏
996 ‎‡2  LC|nb2010003380‏
996 ‎‡2  BNC|981058515045306706‏
996 ‎‡2  ISNI|0000000107850305‏
996 ‎‡2  PLWABN|9812800178005606‏
996 ‎‡2  NLA|000036393462‏
996 ‎‡2  LC|n 91122170‏
996 ‎‡2  BNF|15121094‏
996 ‎‡2  CAOONL|ncf11036790‏
996 ‎‡2  LC|no2017112286‏
996 ‎‡2  ISNI|0000000403513071‏
996 ‎‡2  ISNI|0000000433811555‏
996 ‎‡2  N6I|vtls002701906‏
996 ‎‡2  CAOONL|ncf11366684‏
996 ‎‡2  SIMACOB|45420131‏
996 ‎‡2  LC|n 2015003752‏
996 ‎‡2  NUKAT|n 00078086‏
996 ‎‡2  CAOONL|ncf11223519‏
996 ‎‡2  BIBSYS|90313785‏
996 ‎‡2  LC|n 82089435‏
996 ‎‡2  LIH|LNB:C2GH;=_o__l_‏
996 ‎‡2  NUKAT|n 2009083972‏
996 ‎‡2  NYNYRILM|177293‏
996 ‎‡2  SUDOC|265629209‏
996 ‎‡2  NTA|124897576‏
996 ‎‡2  SIMACOB|198585187‏
996 ‎‡2  LC|n 88156734‏
996 ‎‡2  DNB|173745202‏
996 ‎‡2  BIBSYS|90589920‏
996 ‎‡2  N6I|vtls001336976‏
996 ‎‡2  NUKAT|nx2023772870‏
996 ‎‡2  RERO|A012384869‏
996 ‎‡2  BIBSYS|1081530‏
996 ‎‡2  LC|n 2013024548‏
996 ‎‡2  NLA|000035369577‏
996 ‎‡2  LC|no 97025323‏
996 ‎‡2  BNF|15561166‏
996 ‎‡2  ISNI|0000000028517539‏
996 ‎‡2  N6I|vtls000375061‏
996 ‎‡2  ISNI|000000003536450X‏
996 ‎‡2  ISNI|0000000448933563‏
996 ‎‡2  LC|n 2013073330‏
996 ‎‡2  PLWABN|9813251187805606‏
996 ‎‡2  B2Q|0000071744‏
996 ‎‡2  ICCU|SBNV072828‏
996 ‎‡2  LC|n 87134059‏
996 ‎‡2  J9U|987007605205705171‏
996 ‎‡2  J9U|987007449833305171‏
996 ‎‡2  NLA|000035453795‏
996 ‎‡2  BIBSYS|90566172‏
996 ‎‡2  ISNI|0000000033447096‏
996 ‎‡2  LC|n 2020181323‏
996 ‎‡2  DNB|1114310395‏
996 ‎‡2  NTA|073749826‏
996 ‎‡2  DNB|136701507‏
996 ‎‡2  LC|no2017146330‏
996 ‎‡2  NII|DA03242877‏
996 ‎‡2  ISNI|0000000022964776‏
996 ‎‡2  J9U|987007450817405171‏
996 ‎‡2  LC|n 87120736‏
996 ‎‡2  SIMACOB|264243043‏
996 ‎‡2  LC|n 97113949‏
996 ‎‡2  LC|n 77015170‏
996 ‎‡2  DNB|1157575005‏
996 ‎‡2  BNF|12445365‏
996 ‎‡2  DNB|102006725X‏
996 ‎‡2  ISNI|0000000391549869‏
996 ‎‡2  LC|n 2007036873‏
996 ‎‡2  NLA|000064878914‏
996 ‎‡2  NTA|119246503‏
996 ‎‡2  LC|n 2021044770‏
996 ‎‡2  BNF|12192863‏
996 ‎‡2  ISNI|0000000074462364‏
996 ‎‡2  CAOONL|ncf10229145‏
996 ‎‡2  CAOONL|ncf10213442‏
996 ‎‡2  BIBSYS|90093328‏
996 ‎‡2  LC|n 86008497‏
996 ‎‡2  ISNI|0000000451297932‏
996 ‎‡2  ISNI|0000000045208754‏
996 ‎‡2  DNB|1180506499‏
996 ‎‡2  ISNI|0000000500840613‏
996 ‎‡2  ISNI|0000000075324908‏
996 ‎‡2  SZ|1217816003‏
996 ‎‡2  ISNI|0000000059665518‏
996 ‎‡2  LC|no2013111226‏
996 ‎‡2  J9U|987007423728405171‏
996 ‎‡2  LC|no2003037574‏
996 ‎‡2  LC|nr2006020055‏
996 ‎‡2  CAOONL|ncf10709670‏
996 ‎‡2  NTA|073547263‏
996 ‎‡2  ISNI|0000000109300518‏
996 ‎‡2  LC|no2014042989‏
996 ‎‡2  LC|n 81125140‏
996 ‎‡2  J9U|987007280438005171‏
996 ‎‡2  NLA|000035194175‏
996 ‎‡2  LC|n 91025168‏
996 ‎‡2  NLA|000035408088‏
996 ‎‡2  ISNI|0000000114686347‏
996 ‎‡2  N6I|vtls000006822‏
996 ‎‡2  LC|nr2004017920‏
996 ‎‡2  ISNI|0000000116153739‏
996 ‎‡2  ISNI|0000000075315980‏
996 ‎‡2  LC|n 78008404‏
996 ‎‡2  BNC|981058522426706706‏
996 ‎‡2  ISNI|0000000119432047‏
996 ‎‡2  LC|n 79118955‏
996 ‎‡2  NLA|000035255728‏
996 ‎‡2  LIH|LNB:B1_l_M;=BS‏
996 ‎‡2  CAOONL|ncf13729815‏
996 ‎‡2  NUKAT|n 2012210836‏
996 ‎‡2  CAOONL|ncf11739441‏
996 ‎‡2  ISNI|0000000114492630‏
996 ‎‡2  LC|no2012086206‏
996 ‎‡2  BNF|12392211‏
996 ‎‡2  LC|n 77002955‏
996 ‎‡2  N6I|vtls000299318‏
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏
998 ‎‡a  Murphy, John A.‏ ‎‡2  DNB|1029931143‏ ‎‡3  suggested‏ ‎‡3  standard number‏