VIAF

Virtual International Authority File

Search

Leader 00000nz a2200037n 45 0
001 WKP|Q60160736 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000238.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q60160736‏
024 ‎‡a 0000-0001-7933-9573‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q60160736‏
046 ‎‡f 19780000‏
100 0 ‎‡a Duc Hanh Nguyen‏ ‎‡9 fr‏ ‎‡9 es‏ ‎‡9 ast‏
375 ‎‡a 2‏ ‎‡2 iso5218‏
400 0 ‎‡a Duc Hanh Nguyen‏ ‎‡c researcher ORCID ID = 0000-0001-7933-9573‏ ‎‡9 en‏
400 0 ‎‡a Duc Hanh Nguyen‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's Acceptorless dehydrogenative coupling of alcohols catalysed by ruthenium PNP complexes: Influence of catalyst structure and of hydrogen mass transfer‏
670 ‎‡a Author's An efficient catalytic system for cyclocarbonylation of terpenes into lactones‏
670 ‎‡a Author's Catalytic Conversion of Alcohols into Carboxylic Acid Salts in Water: Scope, Recycling, and Mechanistic Insights‏
670 ‎‡a Author's ChemInform Abstract: Catalytic Conversion of Alcohols into Carboxylic Acid Salts in Water: Scope, Recycling, and Mechanistic Insights‏
670 ‎‡a Author's ChemInform Abstract: Novel C1-Symmetric Dibenzophosphole Ligands: Application in Hydroformylation Reactions‏
670 ‎‡a Author's ChemInform Abstract: Phosphole-Based Ligands in Catalysis‏
670 ‎‡a Author's ChemInform Abstract: Reduction of Secondary and Tertiary Phosphine Oxides to Phosphines‏
670 ‎‡a Author's ChemInform Abstract: Water-Soluble Hydroformylation Catalysis‏
670 ‎‡a Author's Cover Picture: Catalytic Conversion of Alcohols into Carboxylic Acid Salts in Water: Scope, Recycling, and Mechanistic Insights (ChemSusChem 12/2016)‏
670 ‎‡a Author's Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species‏
670 ‎‡a Author's Direct involvement of the acetato ligand in the reductive elimination step of rhodium-catalyzed methanol carbonylation‏
670 ‎‡a Author's Efficient deuterium labelling of alcohols in deuterated water catalyzed by ruthenium pincer complexes‏
670 ‎‡a Author's Efficient palladium–ferrocenylphosphine catalytic systems for allylic amination of monoterpene derivatives‏
670 ‎‡a Author's First Dibenzophospholyl‏
670 ‎‡a Author's First Dibenzophospholyl(diphenylphosphino)methane−Borane Hybrid P−(η2-BH3) Ligand: Synthesis and Rhodium(I) Complex‏
670 ‎‡a Author's H-adamantylphosphinates as universal precursors of P-stereogenic compounds‏
670 ‎‡a Author's Hydride Mobility in Trinuclear Sulfido Clusters with the Core [Rh3‏
670 ‎‡a Author's Hydride Mobility in Trinuclear Sulfido Clusters with the Core [Rh3(μ-H)(μ3-S)2]: Molecular Models for Hydrogen Migration on Metal Sulfide Hydrotreating Catalysts‏
670 ‎‡a Author's Hydride Route for the Palladium-Catalysed Cyclocarbonylation of Monoterpenes‏
670 ‎‡a Author's Hydrosilylation of Terminal Alkynes Catalyzed by a ONO-Pincer Iridium‏
670 ‎‡a Author's Hydrosilylation of Terminal Alkynes Catalyzed by a ONO-Pincer Iridium(III) Hydride Compound: Mechanistic Insights into the Hydrosilylation and Dehydrogenative Silylation Catalysis‏
670 ‎‡a Author's Inside Cover: Oxidative Transformations of Biosourced Alcohols Catalyzed by Earth-Abundant Transition Metals‏
670 ‎‡a Author's Inside Cover: Oxidative Transformations of Biosourced Alcohols Catalyzed by Earth-Abundant Transition Metals (ChemCatChem 14/2017)‏
670 ‎‡a Author's Involvement of an Acetato Ligand in the Reductive Elimination Step of the Rhodium-Catalyzed Methanol Carbonylation‏
670 ‎‡a Author's Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding‏
670 ‎‡a Author's Mechanistic aspects of the stereospecific reduction of chiral hydroxyalkyl phosphinates and phosphine oxides‏
670 ‎‡a Author's Modular Phosphole-Methano-Bridged-Phosphine‏
670 ‎‡a Author's Modular Phosphole-Methano-Bridged-Phosphine(Borane) Ligands. Application to Rhodium-Catalyzed Reactions‏
670 ‎‡a Author's Novel C1-symmetric dibenzophosphole ligands: application in hydroformylation reactions‏
670 ‎‡a Author's Novel phospholyl‏
670 ‎‡a Author's Novel phospholyl(diphenylphosphino)methane-ruthenium complexes: unexpected non-assisted cis to trans isomerization of [RuCl2(κ(2)-P-P')2].‏
670 ‎‡a Author's ONO Dianionic Pincer-Type Ligand Precursors for the Synthesis of σ,π-Cyclooctenyl Iridium(III) Complexes: Formation Mechanism and Coordination Chemistry‏
670 ‎‡a Author's Oxidative Transformations of Biosourced Alcohols Catalyzed by Earth-Abundant Transition Metals‏
670 ‎‡a Author's [Pd(H)(SnCl3)L2]: The key active species in the catalyzed alkoxycarbonylation reaction of terminal alkenes‏
670 ‎‡a Author's Phosphole-based ligands in catalysis‏
670 ‎‡a Author's Reactivity of Rhodium‏
670 ‎‡a Author's Reactivity of Rhodium(I) Complexes Bearing Nitrogen-Containing Ligands toward CH3I: Synthesis and Full Characterization of Neutral cis-[RhX(CO)2(L)] and Acetyl [RhI(μ-I)(COMe)(CO)(L)]2 Complexes‏
670 ‎‡a Author's Reduction of secondary and tertiary phosphine oxides to phosphines‏
670 ‎‡a Author's Reductive Elimination of Anhydrides from Anionic Iodo Acetyl Carboxylato Rhodium Complexes‏
670 ‎‡a Author's Stereospecific Synthesis of α- and β-Hydroxyalkyl P-Stereogenic Phosphine-Boranes and Functionalized Derivatives: Evidence of the PO Activation in the BH3-Mediated Reduction‏
670 ‎‡a Author's Steric Effects in the Oxidative Addition of MeI to a Sulfido-Bridged ZrRh2 Early–Late Heterobimetallic Compound‏
670 ‎‡a Author's Unsaturated Iridium(III) Complexes Supported by a Quinolato–Carboxylato ONO Pincer-Type Ligand: Synthesis, Reactivity, and Catalytic C–H Functionalization‏
670 ‎‡a Author's Unsaturated iridium pyridinedicarboxylate pincer complexes with catalytic activity in borylation of arenes‏
670 ‎‡a Author's Water-Soluble Hydroformylation Catalysis‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/viaf/189587562‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/SUDOC|084136316‏
909 ‎‡a (orcid) 0000000179339573‏ ‎‡9 1‏
919 ‎‡a hydrosilylationofterminalalkynescatalyzedbyaonopinceriridium‏ ‎‡A Hydrosilylation of Terminal Alkynes Catalyzed by a ONO-Pincer Iridium‏ ‎‡9 1‏
919 ‎‡a cheminformabstractcatalyticconversionofalcoholsintocarboxylicacidsaltsinwaterscoperecyclingandmechanisticinsights‏ ‎‡A ChemInform Abstract: Catalytic Conversion of Alcohols into Carboxylic Acid Salts in Water: Scope, Recycling, and Mechanistic Insights‏ ‎‡9 1‏
919 ‎‡a acceptorlessdehydrogenativecouplingofalcoholscatalysedbyrutheniumpnpcomplexesinfluenceofcatalyststructureandofhydrogenmasstransfer‏ ‎‡A Acceptorless dehydrogenative coupling of alcohols catalysed by ruthenium PNP complexes: Influence of catalyst structure and of hydrogen mass transfer‏ ‎‡9 1‏
919 ‎‡a efficientcatalyticsystemforcyclocarbonylationofterpenesintolactones‏ ‎‡A An efficient catalytic system for cyclocarbonylation of terpenes into lactones‏ ‎‡9 1‏
919 ‎‡a catalyticconversionofalcoholsintocarboxylicacidsaltsinwaterscoperecyclingandmechanisticinsights‏ ‎‡A Catalytic Conversion of Alcohols into Carboxylic Acid Salts in Water: Scope, Recycling, and Mechanistic Insights‏ ‎‡9 1‏
919 ‎‡a cheminformabstractnovelc1symmetricdibenzophospholeligandsapplicationinhydroformylationreactions‏ ‎‡A ChemInform Abstract: Novel C1-Symmetric Dibenzophosphole Ligands: Application in Hydroformylation Reactions‏ ‎‡9 1‏
919 ‎‡a cheminformabstractphospholebasedligandsincatalysis‏ ‎‡A ChemInform Abstract: Phosphole-Based Ligands in Catalysis‏ ‎‡9 1‏
919 ‎‡a cheminformabstractreductionofsecondaryandtertiaryphosphineoxidestophosphines‏ ‎‡A ChemInform Abstract: Reduction of Secondary and Tertiary Phosphine Oxides to Phosphines‏ ‎‡9 1‏
919 ‎‡a cheminformabstractwatersolublehydroformylationcatalysis‏ ‎‡A ChemInform Abstract: Water-Soluble Hydroformylation Catalysis‏ ‎‡9 1‏
919 ‎‡a coverpicturecatalyticconversionofalcoholsintocarboxylicacidsaltsinwaterscoperecyclingandmechanisticinsightschemsuschem12‏ ‎‡A Cover Picture: Catalytic Conversion of Alcohols into Carboxylic Acid Salts in Water: Scope, Recycling, and Mechanistic Insights (ChemSusChem 12/2016)‏ ‎‡9 1‏
919 ‎‡a deepermechanisticinsightintorupincermediatedacceptorlessdehydrogenativecouplingofalcoholsexchangesintermediatesanddeactivationspecies‏ ‎‡A Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species‏ ‎‡9 1‏
919 ‎‡a directinvolvementoftheacetatoligandinthereductiveeliminationstepofrhodiumcatalyzedmethanolcarbonylation‏ ‎‡A Direct involvement of the acetato ligand in the reductive elimination step of rhodium-catalyzed methanol carbonylation‏ ‎‡9 1‏
919 ‎‡a efficientdeuteriumlabellingofalcoholsindeuteratedwatercatalyzedbyrutheniumpincercomplexes‏ ‎‡A Efficient deuterium labelling of alcohols in deuterated water catalyzed by ruthenium pincer complexes‏ ‎‡9 1‏
919 ‎‡a efficientpalladiumferrocenylphosphinecatalyticsystemsforallylicaminationofmonoterpenederivatives‏ ‎‡A Efficient palladium–ferrocenylphosphine catalytic systems for allylic amination of monoterpene derivatives‏ ‎‡9 1‏
919 ‎‡a 1dibenzophospholyl‏ ‎‡A First Dibenzophospholyl‏ ‎‡9 1‏
919 ‎‡a 1dibenzophospholyldiphenylphosphinomethaneboranehybridpη2bh3ligandsynthesisandrhodium1complex‏ ‎‡A First Dibenzophospholyl(diphenylphosphino)methane−Borane Hybrid P−(η2-BH3) Ligand: Synthesis and Rhodium(I) Complex‏ ‎‡9 1‏
919 ‎‡a hydridemobilityintrinuclearsulfidoclusterswiththecorerh3‏ ‎‡A Hydride Mobility in Trinuclear Sulfido Clusters with the Core [Rh3‏ ‎‡9 1‏
919 ‎‡a hydridemobilityintrinuclearsulfidoclusterswiththecoremolecularmodelsforhydrogenmigrationonmetalsulfidehydrotreatingcatalysts‏ ‎‡A Hydride Mobility in Trinuclear Sulfido Clusters with the Core [Rh3(μ-H)(μ3-S)2]: Molecular Models for Hydrogen Migration on Metal Sulfide Hydrotreating Catalysts‏ ‎‡9 1‏
919 ‎‡a hydriderouteforthepalladiumcatalysedcyclocarbonylationofmonoterpenes‏ ‎‡A Hydride Route for the Palladium-Catalysed Cyclocarbonylation of Monoterpenes‏ ‎‡9 1‏
919 ‎‡a hydrosilylationofterminalalkynescatalyzedbyaonopinceriridium3hydridecompoundmechanisticinsightsintothehydrosilylationanddehydrogenativesilylationcatalysis‏ ‎‡A Hydrosilylation of Terminal Alkynes Catalyzed by a ONO-Pincer Iridium(III) Hydride Compound: Mechanistic Insights into the Hydrosilylation and Dehydrogenative Silylation Catalysis‏ ‎‡9 1‏
919 ‎‡a insidecoveroxidativetransformationsofbiosourcedalcoholscatalyzedbyearthabundanttransitionmetals‏ ‎‡A Inside Cover: Oxidative Transformations of Biosourced Alcohols Catalyzed by Earth-Abundant Transition Metals‏ ‎‡9 1‏
919 ‎‡a insidecoveroxidativetransformationsofbiosourcedalcoholscatalyzedbyearthabundanttransitionmetalschemcatchem14‏ ‎‡A Inside Cover: Oxidative Transformations of Biosourced Alcohols Catalyzed by Earth-Abundant Transition Metals (ChemCatChem 14/2017)‏ ‎‡9 1‏
919 ‎‡a involvementofanacetatoligandinthereductiveeliminationstepoftherhodiumcatalyzedmethanolcarbonylation‏ ‎‡A Involvement of an Acetato Ligand in the Reductive Elimination Step of the Rhodium-Catalyzed Methanol Carbonylation‏ ‎‡9 1‏
919 ‎‡a manganesepincercomplexesforthebasefreeacceptorlessdehydrogenativecouplingofalcoholstoestersdevelopmentscopeandunderstanding‏ ‎‡A Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding‏ ‎‡9 1‏
919 ‎‡a mechanisticaspectsofthestereospecificreductionofchiralhydroxyalkylphosphinatesandphosphineoxides‏ ‎‡A Mechanistic aspects of the stereospecific reduction of chiral hydroxyalkyl phosphinates and phosphine oxides‏ ‎‡9 1‏
919 ‎‡a modularphospholemethanobridgedphosphine‏ ‎‡A Modular Phosphole-Methano-Bridged-Phosphine‏ ‎‡9 1‏
919 ‎‡a modularphospholemethanobridgedphosphineboraneligandsapplicationtorhodiumcatalyzedreactions‏ ‎‡A Modular Phosphole-Methano-Bridged-Phosphine(Borane) Ligands. Application to Rhodium-Catalyzed Reactions‏ ‎‡9 1‏
919 ‎‡a novelc1symmetricdibenzophospholeligandsapplicationinhydroformylationreactions‏ ‎‡A Novel C1-symmetric dibenzophosphole ligands: application in hydroformylation reactions‏ ‎‡9 1‏
919 ‎‡a novelphospholyl‏ ‎‡A Novel phospholyl‏ ‎‡9 1‏
919 ‎‡a novelphospholyldiphenylphosphinomethanerutheniumcomplexesunexpectednonassistedcistotransisomerizationof‏ ‎‡A Novel phospholyl(diphenylphosphino)methane-ruthenium complexes: unexpected non-assisted cis to trans isomerization of [RuCl2(κ(2)-P-P')2].‏ ‎‡9 1‏
919 ‎‡a onodianionicpincertypeligandprecursorsforthesynthesisofσπcyclooctenyliridium3complexesformationmechanismandcoordinationchemistry‏ ‎‡A ONO Dianionic Pincer-Type Ligand Precursors for the Synthesis of σ,π-Cyclooctenyl Iridium(III) Complexes: Formation Mechanism and Coordination Chemistry‏ ‎‡9 1‏
919 ‎‡a oxidativetransformationsofbiosourcedalcoholscatalyzedbyearthabundanttransitionmetals‏ ‎‡A Oxidative Transformations of Biosourced Alcohols Catalyzed by Earth-Abundant Transition Metals‏ ‎‡9 1‏
919 ‎‡a keyactivespeciesinthecatalyzedalkoxycarbonylationreactionofterminalalkenes‏ ‎‡A [Pd(H)(SnCl3)L2]: The key active species in the catalyzed alkoxycarbonylation reaction of terminal alkenes‏ ‎‡9 1‏
919 ‎‡a phospholebasedligandsincatalysis‏ ‎‡A Phosphole-based ligands in catalysis‏ ‎‡9 1‏
919 ‎‡a reactivityofrhodium‏ ‎‡A Reactivity of Rhodium‏ ‎‡9 1‏
919 ‎‡a reactivityofrhodium1complexesbearingnitrogencontainingligandstowardch3isynthesisandfullcharacterizationofneutralcisandacetyl2complexes‏ ‎‡A Reactivity of Rhodium(I) Complexes Bearing Nitrogen-Containing Ligands toward CH3I: Synthesis and Full Characterization of Neutral cis-[RhX(CO)2(L)] and Acetyl [RhI(μ-I)(COMe)(CO)(L)]2 Complexes‏ ‎‡9 1‏
919 ‎‡a reductionofsecondaryandtertiaryphosphineoxidestophosphines‏ ‎‡A Reduction of secondary and tertiary phosphine oxides to phosphines‏ ‎‡9 1‏
919 ‎‡a reductiveeliminationofanhydridesfromanioniciodoacetylcarboxylatorhodiumcomplexes‏ ‎‡A Reductive Elimination of Anhydrides from Anionic Iodo Acetyl Carboxylato Rhodium Complexes‏ ‎‡9 1‏
919 ‎‡a stereospecificsynthesisofαandβhydroxyalkylpstereogenicphosphineboranesandfunctionalizedderivativesevidenceofthepoactivationinthebh3mediatedreduction‏ ‎‡A Stereospecific Synthesis of α- and β-Hydroxyalkyl P-Stereogenic Phosphine-Boranes and Functionalized Derivatives: Evidence of the PO Activation in the BH3-Mediated Reduction‏ ‎‡9 1‏
919 ‎‡a stericeffectsintheoxidativeadditionofmeitoasulfidobridgedzrrh2earlylateheterobimetalliccompound‏ ‎‡A Steric Effects in the Oxidative Addition of MeI to a Sulfido-Bridged ZrRh2 Early–Late Heterobimetallic Compound‏ ‎‡9 1‏
919 ‎‡a unsaturatediridium3complexessupportedbyaquinolatocarboxylatoonopincertypeligandsynthesisreactivityandcatalytic100hfunctionalization‏ ‎‡A Unsaturated Iridium(III) Complexes Supported by a Quinolato–Carboxylato ONO Pincer-Type Ligand: Synthesis, Reactivity, and Catalytic C–H Functionalization‏ ‎‡9 1‏
919 ‎‡a unsaturatediridiumpyridinedicarboxylatepincercomplexeswithcatalyticactivityinborylationofarenes‏ ‎‡A Unsaturated iridium pyridinedicarboxylate pincer complexes with catalytic activity in borylation of arenes‏ ‎‡9 1‏
919 ‎‡a watersolublehydroformylationcatalysis‏ ‎‡A Water-Soluble Hydroformylation Catalysis‏ ‎‡9 1‏
919 ‎‡a hadamantylphosphinatesasuniversalprecursorsofpstereogeniccompounds‏ ‎‡A H-adamantylphosphinates as universal precursors of P-stereogenic compounds‏ ‎‡9 1‏
943 ‎‡a 201x‏ ‎‡A 2016‏ ‎‡9 2‏
946 ‎‡a a‏ ‎‡9 1‏
996 ‎‡2 NUKAT|n 99005631‏
996 ‎‡2 LC|n 88205576‏
996 ‎‡2 NUKAT|n 2019217996‏
996 ‎‡2 ISNI|0000000000536551‏
996 ‎‡2 ISNI|0000000437151910‏
996 ‎‡2 SUDOC|26141061X‏
996 ‎‡2 LC|n 94062858‏
996 ‎‡2 DNB|1046207652‏
996 ‎‡2 LC|nr2002031312‏
996 ‎‡2 LC|n 2017220014‏
996 ‎‡2 ISNI|0000000045996658‏
996 ‎‡2 LC|nr 96029685‏
996 ‎‡2 ISNI|0000000083555845‏
996 ‎‡2 ISNI|0000000029801590‏
996 ‎‡2 DNB|1190739259‏
996 ‎‡2 NUKAT|n 2010110801‏
996 ‎‡2 DNB|1239846649‏
996 ‎‡2 LC|no2017124857‏
996 ‎‡2 DNB|1189759942‏
996 ‎‡2 ISNI|000000006304700X‏
996 ‎‡2 LC|no2011193714‏
996 ‎‡2 LC|no2010162722‏
996 ‎‡2 NUKAT|nx2023162747‏
996 ‎‡2 DNB|1158164157‏
996 ‎‡2 SUDOC|131906038‏
996 ‎‡2 SUDOC|254172113‏
996 ‎‡2 DBC|87097969010059‏
996 ‎‡2 DNB|142473715‏
996 ‎‡2 ISNI|0000000049524375‏
996 ‎‡2 LC|n 90621118‏
996 ‎‡2 SUDOC|147363233‏
996 ‎‡2 BNF|16991208‏
996 ‎‡2 LC|no2015120800‏
996 ‎‡2 NII|DA03007254‏
996 ‎‡2 BNF|14512257‏
996 ‎‡2 ISNI|0000000030283583‏
996 ‎‡2 LC|nr2007007803‏
996 ‎‡2 BNF|13072109‏
996 ‎‡2 LC|n 85275720‏
996 ‎‡2 LC|n 97124896‏
996 ‎‡2 ISNI|000000004419600X‏
996 ‎‡2 SUDOC|096702656‏
996 ‎‡2 SUDOC|111400384‏
996 ‎‡2 ISNI|0000000002953666‏
996 ‎‡2 DNB|133755797‏
996 ‎‡2 DNB|1158375468‏
996 ‎‡2 LC|n 2001057598‏
996 ‎‡2 DNB|1159216045‏
996 ‎‡2 DNB|1124708480‏
996 ‎‡2 LC|no2015134047‏
996 ‎‡2 ISNI|0000000033525330‏
996 ‎‡2 DNB|1287816029‏
996 ‎‡2 DNB|128449960X‏
996 ‎‡2 NII|DA13997695‏
996 ‎‡2 BNF|15014349‏
996 ‎‡2 DNB|112982085‏
996 ‎‡2 ISNI|0000000009225637‏
996 ‎‡2 ISNI|0000000383345380‏
996 ‎‡2 NDL|00835551‏
996 ‎‡2 DNB|1158705131‏
996 ‎‡2 LC|no2002097012‏
996 ‎‡2 ISNI|0000000047267782‏
996 ‎‡2 BNF|15763664‏
996 ‎‡2 DNB|1154416453‏
996 ‎‡2 LC|no2007079944‏
996 ‎‡2 LC|no2008030219‏
996 ‎‡2 LC|no2004082921‏
996 ‎‡2 ISNI|0000000094544412‏
996 ‎‡2 LC|n 88649804‏
996 ‎‡2 ISNI|000000002665277X‏
996 ‎‡2 LC|n 2022008559‏
996 ‎‡2 SUDOC|031055036‏
996 ‎‡2 ISNI|0000000400339645‏
996 ‎‡2 LC|nr2001047100‏
996 ‎‡2 DNB|1078269831‏
996 ‎‡2 DNB|1231578750‏
996 ‎‡2 SUDOC|161016081‏
996 ‎‡2 BNF|14565900‏
996 ‎‡2 ISNI|000000005488165X‏
996 ‎‡2 NTA|132079909‏
996 ‎‡2 BNF|12796464‏
996 ‎‡2 ISNI|000000006706865X‏
996 ‎‡2 DNB|1018361138‏
996 ‎‡2 CAOONL|ncf10177931‏
996 ‎‡2 SUDOC|171778278‏
996 ‎‡2 DNB|1157426778‏
996 ‎‡2 ISNI|0000000063052677‏
996 ‎‡2 SUDOC|092118658‏
996 ‎‡2 CAOONL|ncf10455766‏
996 ‎‡2 DNB|1159337497‏
996 ‎‡2 LC|nr2002012409‏
996 ‎‡2 ISNI|000000038687929X‏
996 ‎‡2 DNB|142908053‏
996 ‎‡2 DNB|1267857935‏
996 ‎‡2 LC|nr2002010346‏
996 ‎‡2 BNF|16985807‏
996 ‎‡2 SUDOC|087703661‏
996 ‎‡2 DNB|1158191502‏
996 ‎‡2 LC|nr2002010741‏
996 ‎‡2 SUDOC|248912461‏
996 ‎‡2 SUDOC|280770693‏
996 ‎‡2 ISNI|0000000042431205‏
996 ‎‡2 ISNI|0000000073101751‏
996 ‎‡2 NII|DA13423685‏
996 ‎‡2 NII|DA17944409‏
996 ‎‡2 J9U|987012502742905171‏
996 ‎‡2 LC|n 96070045‏
996 ‎‡2 ISNI|0000000384809861‏
996 ‎‡2 LC|n 2020035557‏
996 ‎‡2 LC|n 2010016610‏
996 ‎‡2 LC|no2019047446‏
996 ‎‡2 ISNI|0000000035626696‏
996 ‎‡2 DNB|1159295158‏
996 ‎‡2 DNB|1249773016‏
996 ‎‡2 SUDOC|177125500‏
996 ‎‡2 NII|DA19614471‏
996 ‎‡2 ISNI|0000000051634098‏
996 ‎‡2 SUDOC|195235649‏
996 ‎‡2 DNB|1277976090‏
996 ‎‡2 LC|n 2006019805‏
996 ‎‡2 SUDOC|17885610X‏
996 ‎‡2 LC|nb2018010413‏
996 ‎‡2 NDL|001227907‏
996 ‎‡2 LC|nr 97024724‏
996 ‎‡2 DNB|1272803546‏
996 ‎‡2 SUDOC|243297653‏
996 ‎‡2 LC|n 90618507‏
996 ‎‡2 DNB|1274650828‏
996 ‎‡2 SUDOC|177212020‏
996 ‎‡2 LC|n 2018021095‏
996 ‎‡2 DNB|1297269411‏
996 ‎‡2 LC|n 2020062873‏
996 ‎‡2 DNB|170295214‏
996 ‎‡2 DNB|1279674911‏
996 ‎‡2 LC|no2016164723‏
996 ‎‡2 LC|n 95036236‏
996 ‎‡2 SUDOC|124601928‏
996 ‎‡2 DNB|1158420811‏
996 ‎‡2 SUDOC|276380665‏
996 ‎‡2 NUKAT|n 2006125505‏
996 ‎‡2 LC|n 2006209797‏
996 ‎‡2 ISNI|000000004095925X‏
996 ‎‡2 DNB|1158258755‏
996 ‎‡2 LC|n 95047524‏
996 ‎‡2 J9U|987007349345205171‏
996 ‎‡2 ISNI|0000000000396405‏
996 ‎‡2 LC|nr 99034472‏
996 ‎‡2 LC|n 90665539‏
996 ‎‡2 LC|no2007149569‏
996 ‎‡2 ISNI|0000000047200780‏
996 ‎‡2 DNB|115822348X‏
996 ‎‡2 LC|n 2008079232‏
996 ‎‡2 LC|nr 96024126‏
996 ‎‡2 LC|no2004084186‏
996 ‎‡2 ISNI|0000000076414374‏
996 ‎‡2 LC|nr 96020457‏
996 ‎‡2 LC|n 97065249‏
996 ‎‡2 DNB|1159314462‏
996 ‎‡2 DNB|1201913233‏
996 ‎‡2 ISNI|0000000054456442‏
996 ‎‡2 LC|n 2006073303‏
996 ‎‡2 SUDOC|224898329‏
996 ‎‡2 CAOONL|ncf10716658‏
996 ‎‡2 LC|no2006104413‏
996 ‎‡2 DNB|1240920245‏
996 ‎‡2 DNB|1311762094‏
996 ‎‡2 NUKAT|n 2022004904‏
996 ‎‡2 DNB|134231341‏
996 ‎‡2 ISNI|0000000031171903‏
996 ‎‡2 DNB|1299766234‏
996 ‎‡2 LC|n 99055292‏
996 ‎‡2 LC|n 94123085‏
996 ‎‡2 DNB|1158291035‏
996 ‎‡2 NTA|292077823‏
996 ‎‡2 DNB|115731631X‏
996 ‎‡2 LC|nb2006013867‏
996 ‎‡2 DNB|1158577109‏
996 ‎‡2 ISNI|000000004427977X‏
996 ‎‡2 ISNI|0000000049455445‏
996 ‎‡2 LC|nr 94024305‏
996 ‎‡2 DNB|1057762539‏
996 ‎‡2 LC|no2013039505‏
996 ‎‡2 DNB|1159245878‏
996 ‎‡2 BNF|16980727‏
996 ‎‡2 LC|n 87906200‏
996 ‎‡2 SUDOC|098211374‏
996 ‎‡2 DNB|1158386516‏
996 ‎‡2 ISNI|0000000077517922‏
996 ‎‡2 ISNI|0000000000051036‏
996 ‎‡2 DNB|1315336227‏
996 ‎‡2 ISNI|0000000021417471‏
996 ‎‡2 SUDOC|241797411‏
996 ‎‡2 SUDOC|197817602‏
996 ‎‡2 NII|DA18235081‏
996 ‎‡2 LC|nr 00018047‏
996 ‎‡2 DNB|115929304X‏
996 ‎‡2 ICCU|IEIV005996‏
996 ‎‡2 SUDOC|052619575‏
996 ‎‡2 ISNI|0000000036168535‏
996 ‎‡2 ISNI|0000000398026075‏
996 ‎‡2 SUDOC|147399254‏
996 ‎‡2 LC|no2002004904‏
996 ‎‡2 J9U|987007356681605171‏
996 ‎‡2 LC|nb2023006665‏
996 ‎‡2 LC|n 2005209207‏
996 ‎‡2 BNF|17842406‏
996 ‎‡2 LC|no2012003329‏
996 ‎‡2 NII|DA18176095‏
996 ‎‡2 DNB|1252508751‏
996 ‎‡2 LC|no2008075988‏
996 ‎‡2 NUKAT|n 97088214‏
996 ‎‡2 NII|DA17667284‏
996 ‎‡2 SUDOC|242621503‏
996 ‎‡2 DNB|1237375444‏
996 ‎‡2 SUDOC|093622880‏
996 ‎‡2 SUDOC|250595931‏
996 ‎‡2 ISNI|0000000382423885‏
996 ‎‡2 SUDOC|175377189‏
996 ‎‡2 LC|no2010084929‏
996 ‎‡2 DNB|1158128312‏
996 ‎‡2 LC|n 96068734‏
996 ‎‡2 ISNI|0000000076818467‏
996 ‎‡2 SUDOC|155605356‏
996 ‎‡2 LC|no2004111525‏
996 ‎‡2 SZ|134231341‏
996 ‎‡2 DNB|1251570348‏
996 ‎‡2 ISNI|0000000002113114‏
996 ‎‡2 ISNI|0000000050089550‏
996 ‎‡2 LC|n 2007035642‏
996 ‎‡2 LC|nr 98024687‏
996 ‎‡2 LC|n 2006221527‏
996 ‎‡2 ISNI|0000000008608732‏
996 ‎‡2 DNB|1158721552‏
996 ‎‡2 LC|nr 97036607‏
996 ‎‡2 DNB|1034760394‏
996 ‎‡2 DNB|1061958175‏
996 ‎‡2 LC|no2010037056‏
996 ‎‡2 DNB|1138732389‏
996 ‎‡2 BNF|17121686‏
996 ‎‡2 DNB|1159245932‏
996 ‎‡2 J9U|987007315696305171‏
996 ‎‡2 NII|DA10704757‏
996 ‎‡2 DNB|1318110300‏
996 ‎‡2 SUDOC|248867040‏
996 ‎‡2 SUDOC|119182394‏
996 ‎‡2 ISNI|0000000115612673‏
996 ‎‡2 LC|n 93104685‏
996 ‎‡2 LC|n 2014060187‏
996 ‎‡2 LC|n 82129756‏
996 ‎‡2 ISNI|0000000496987400‏
997 ‎‡a 1978 0 lived 0000 0‏ ‎‡9 1‏
998 ‎‡a Nguyen, Duc Hanh,‏ ‎‡2 SUDOC|084136316‏ ‎‡3 suggested‏ ‎‡3 title: (0.78, 'hydriderouteforthepalladiumcatlysedalcoxtcarbonylationandcyclocarbonylationofmontermenesextensiontoallylicamination', 'hydriderouteforthepalladiumcatalysedcyclocarbonylationofmonoterpenes')‏