VIAF

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Leader     00000nz a2200037n 45 0
001     WKP|Q37831616  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241121000315.0
008     241121nneanz||abbn n and d
035 ‎‡a  (WKP)Q37831616‏
024 ‎‡a  0000-0001-5245-7748‏ ‎‡2  orcid‏
035 ‎‡a  (OCoLC)Q37831616‏
043 ‎‡c  NL‏
046 ‎‡f  19510000‏
100 0 ‎‡a  Johannes G de Vries‏ ‎‡c  wetenschapper‏ ‎‡9  nl‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  Johannes G. de Vries‏ ‎‡c  chimiste néerlandais‏ ‎‡9  fr‏
400 0 ‎‡a  Johannes de Vries‏ ‎‡c  Dutch chemist‏ ‎‡9  en‏
400 0 ‎‡a  Johannes de Vries‏ ‎‡c  hulumtues‏ ‎‡9  sq‏
400 0 ‎‡a  Johannes Gerardus de Vries‏ ‎‡9  sk‏
400 0 ‎‡a  Johannes Gerardus de Vries‏ ‎‡c  nizozemský profesor chemie, specialista v oblasti katalýzy‏ ‎‡9  cs‏
400 0 ‎‡a  Johannes G de Vries‏ ‎‡c  químico neerlandés‏ ‎‡9  es‏
670 ‎‡a  Author's 3,3'-Diaryl-BINOL phosphoric acids as enantioselective extractants of benzylic primary amines‏
670 ‎‡a  Author's A metal-ligand cooperative pathway for intermolecular oxa-Michael additions to unsaturated nitriles‏
670 ‎‡a  Author's A Simple and Effective Co-Catalyst for Ring-Closing Enyne Metathesis Using Grubbs I type Catalysts: A Practical Alternative to “Mori’s Conditions”‏
670 ‎‡a  Author's Achiral ligands dramatically enhance rate and enantioselectivity in the Rh/phosphoramidite-catalyzed hydrogenation of alpha,beta-disubstituted unsaturated acids‏
670 ‎‡a  Author's Additive-Free Isomerization of Allylic Alcohols to Ketones with a Cobalt PNP Pincer Catalyst‏
670 ‎‡a  Author's Advanced Model Compounds for Understanding Acid-Catalyzed Lignin Depolymerization: Identification of Renewable Aromatics and a Lignin-Derived Solvent‏
670 ‎‡a  Author's Alkene isomerisation catalysed by a ruthenium PNN pincer complex‏
670 ‎‡a  Author's Aromatic monomers by in situ conversion of reactive intermediates in the acid-catalyzed depolymerization of lignin.‏
670 ‎‡a  Author's Asymmetric Hydrogenation of 3-Substituted Pyridinium Salts‏
670 ‎‡a  Author's Asymmetric hydrogenation using monodentate phosphoramidite ligands‏
670 ‎‡a  Author's At the frontier between heterogeneous and homogeneous catalysis: hydrogenation of olefins and alkynes with soluble iron nanoparticles.‏
670 ‎‡a  Author's Base-Free Iron Catalyzed Transfer Hydrogenation of Esters Using EtOH as Hydrogen Source‏
670 ‎‡a  Author's Bio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediate‏
670 ‎‡a  Author's Caprolactam from Renewable Resources: Catalytic Conversion of 5-Hydroxymethylfurfural into Caprolactone‏
670 ‎‡a  Author's Catalytic Approaches to Monomers for Polymers Based on Renewables‏
670 ‎‡a  Author's Catalytic regioselective oxidation of glycosides‏
670 ‎‡a  Author's Chiral separation by enantioselective liquid-liquid extraction‏
670 ‎‡a  Author's Chiral separation of substituted phenylalanine analogues using chiral palladium phosphine complexes with enantioselective liquid-liquid extraction‏
670 ‎‡a  Author's Chiral separation of underivatized amino acids by reactive extraction with palladium-BINAP complexes.‏
670 ‎‡a  Author's Cyclopentanone Derivatives from 5-Hydroxymethylfurfural via 1-Hydroxyhexane-2,5-dione as Intermediate‏
670 ‎‡a  Author's Deuteration enhances catalyst lifetime in palladium-catalysed alcohol oxidation‏
670 ‎‡a  Author's Dynamic kinetic resolution of racemic beta-haloalcohols: direct access to enantioenriched epoxides‏
670 ‎‡a  Author's Efficient formation of benzylic quaternary centers via palladium catalysis‏
670 ‎‡a  Author's Efficient Synthesis of Biomass‐Derived N‐Substituted 2‐Hydroxymethyl‐5‐Methyl‐Pyrroles in Two Steps from 5‐Hydroxymethylfurfural‏
670 ‎‡a  Author's Enantio- and diastereoselective synthesis of γ-amino alcohols‏
670 ‎‡a  Author's Enantiomerically pure beta-phenylalanine analogues from alpha-beta-phenylalanine mixtures in a single reactive extraction step‏
670 ‎‡a  Author's Enantioselective Rh-catalyzed hydrogenation of N-formyl dehydroamino esters with monodentate phosphoramidite ligands‏
670 ‎‡a  Author's Highly Efficient and Robust Enantioselective Liquid-Liquid Extraction of 1,2-Amino Alcohols utilizing VAPOL- and VANOL-based Phosphoric Acid Hosts‏
670 ‎‡a  Author's Highly efficient enantioselective liquid-liquid extraction of 1,2-amino-alcohols using SPINOL based phosphoric acid hosts‏
670 ‎‡a  Author's Highly enantioselective conjugate additions of potassium organotrifluoroborates to enones by use of monodentate phosphoramidite ligands‏
670 ‎‡a  Author's Highly Enantioselective Rhodium-Catalyzed Hydrogenation with Monodentate Ligands‏
670 ‎‡a  Author's Hydration of nitriles using a metal-ligand cooperative ruthenium pincer catalyst‏
670 ‎‡a  Author's Hydrogenation of Polyesters to Polyether Polyols‏
670 ‎‡a  Author's Hydroxymethylfurfural, a versatile platform chemical made from renewable resources.‏
670 ‎‡a  Author's Improvement in the Palladium-Catalyzed Miyaura Borylation Reaction by Optimization of the Base: Scope and Mechanistic Study‏
670 ‎‡a  Author's Iridium/monodentate phosphoramidite catalyzed asymmetric hydrogenation of N-aryl imines.‏
670 ‎‡a  Author's Isomerization of Allylic Alcohols to Ketones Catalyzed by Well-Defined Iron PNP Pincer Catalysts.‏
670 ‎‡a  Author's Manganese PNP-pincer catalyzed isomerization of allylic/homo-allylic alcohols to ketones – activity, selectivity, efficiency‏
670 ‎‡a  Author's Metal Triflates for the Production of Aromatics from Lignin.‏
670 ‎‡a  Author's Nylon Intermediates from Bio-Based Levulinic Acid‏
670 ‎‡a  Author's Oxa-Michael Addition to α,β-Unsaturated Nitriles: An Expedient Route to γ-Amino Alcohols and Derivatives‏
670 ‎‡a  Author's Palladium(0)/NHC-Catalyzed Reductive Heck Reaction of Enones: A Detailed Mechanistic Study‏
670 ‎‡a  Author's Palladium-catalyzed asymmetric quaternary stereocenter formation‏
670 ‎‡a  Author's Pd-NHC catalyzed conjugate addition versus the Mizoroki-Heck reaction‏
670 ‎‡a  Author's PipPhos and MorfPhos: privileged monodentate phosphoramidite ligands for rhodium-catalyzed asymmetric hydrogenation‏
670 ‎‡a  Author's Platinum-catalyzed selective hydration of hindered nitriles and nitriles with acid- or base-sensitive groups‏
670 ‎‡a  Author's Properties of Novel Polyesters Made from Renewable 1,4-Pentanediol‏
670 ‎‡a  Author's Rhenium-catalyzed deoxydehydration of renewable triols derived from sugars‏
670 ‎‡a  Author's Selective Base-free Transfer Hydrogenation of α,β-Unsaturated Carbonyl Compounds using iPrOH or EtOH as Hydrogen Source.‏
670 ‎‡a  Author's Selective conversion of polyenes to monoenes by RuCl(3) -catalyzed transfer hydrogenation: the case of cashew nutshell liquid‏
670 ‎‡a  Author's Selective Hydrogenation of α,β-Unsaturated Aldehydes and Ketones by Air-Stable Ruthenium NNS Complexes‏
670 ‎‡a  Author's Synthesis and application in asymmetric C-C bond formation of solution phase ligand libraries of monodentate phosphoramidites‏
670 ‎‡a  Author's Synthesis, characterization and catalytic activity of novel ruthenium complexes bearing NNN click based ligands‏
670 ‎‡a  Author's Synthesis of <i>N</i>-Substituted 3-Hydroxypyridinium Salts from Bioderived 5-Hydroxymethylfurfural in Water‏
670 ‎‡a  Author's Synthesis of renewable fine-chemical building blocks by reductive coupling between furfural derivatives and terpenes‏
670 ‎‡a  Author's Synthesis of solution-phase phosphoramidite and phosphite ligand libraries and their in situ screening in the rhodium-catalyzed asymmetric addition of arylboronic acids‏
670 ‎‡a  Author's Synthesis of α-keto aldehydes <i>via</i> selective Cu(<scp>i</scp>)-catalyzed oxidation of α-hydroxy ketones‏
670 ‎‡a  Author's Unravelling the reaction path of rhodium-MonoPhos-catalysed olefin hydrogenation‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/processed/DNB|132252880‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/processed/NUKAT|n 2007089212‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/processed/ISNI|0000000115919640‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/viaf/7713622‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/processed/NKC|mub20201064281‏
670 ‎‡a  wikidata authority control‏ ‎‡u  https://viaf.org/processed/SUDOC|111806305‏
909 ‎‡a  (orcid) 0000000152457748‏ ‎‡9  1‏
919 ‎‡a  chiralseparationbyenantioselectiveliquidliquidextraction‏ ‎‡A  Chiral separation by enantioselective liquid-liquid extraction‏ ‎‡9  1‏
919 ‎‡a  chiralseparationofsubstitutedphenylalanineanaloguesusingchiralpalladiumphosphinecomplexeswithenantioselectiveliquidliquidextraction‏ ‎‡A  Chiral separation of substituted phenylalanine analogues using chiral palladium phosphine complexes with enantioselective liquid-liquid extraction‏ ‎‡9  1‏
919 ‎‡a  chiralseparationofunderivatizedaminoacidsbyreactiveextractionwithpalladiumbinapcomplexes‏ ‎‡A  Chiral separation of underivatized amino acids by reactive extraction with palladium-BINAP complexes.‏ ‎‡9  1‏
919 ‎‡a  cyclopentanonederivativesfrom5hydroxymethylfurfuralvia1hydroxyhexane25dioneasintermediate‏ ‎‡A  Cyclopentanone Derivatives from 5-Hydroxymethylfurfural via 1-Hydroxyhexane-2,5-dione as Intermediate‏ ‎‡9  1‏
919 ‎‡a  deuterationenhancescatalystlifetimeinpalladiumcatalysedalcoholoxidation‏ ‎‡A  Deuteration enhances catalyst lifetime in palladium-catalysed alcohol oxidation‏ ‎‡9  1‏
919 ‎‡a  dynamickineticresolutionofracemicbetahaloalcoholsdirectaccesstoenantioenrichedepoxides‏ ‎‡A  Dynamic kinetic resolution of racemic beta-haloalcohols: direct access to enantioenriched epoxides‏ ‎‡9  1‏
919 ‎‡a  efficientformationofbenzylicquaternarycentersviapalladiumcatalysis‏ ‎‡A  Efficient formation of benzylic quaternary centers via palladium catalysis‏ ‎‡9  1‏
919 ‎‡a  efficientsynthesisofbiomassderivednsubstituted2hydroxymethyl5methylpyrrolesin2stepsfrom5hydroxymethylfurfural‏ ‎‡A  Efficient Synthesis of Biomass‐Derived N‐Substituted 2‐Hydroxymethyl‐5‐Methyl‐Pyrroles in Two Steps from 5‐Hydroxymethylfurfural‏ ‎‡9  1‏
919 ‎‡a  enantioanddiastereoselectivesynthesisofγaminoalcohols‏ ‎‡A  Enantio- and diastereoselective synthesis of γ-amino alcohols‏ ‎‡9  1‏
919 ‎‡a  enantiomericallypurebetaphenylalanineanaloguesfromalphabetaphenylalaninemixturesinasinglereactiveextractionstep‏ ‎‡A  Enantiomerically pure beta-phenylalanine analogues from alpha-beta-phenylalanine mixtures in a single reactive extraction step‏ ‎‡9  1‏
919 ‎‡a  enantioselectiverhcatalyzedhydrogenationofnformyldehydroaminoesterswithmonodentatephosphoramiditeligands‏ ‎‡A  Enantioselective Rh-catalyzed hydrogenation of N-formyl dehydroamino esters with monodentate phosphoramidite ligands‏ ‎‡9  1‏
919 ‎‡a  highlyefficientandrobustenantioselectiveliquidliquidextractionof12aminoalcoholsutilizingvapolandvanolbasedphosphoricacidhosts‏ ‎‡A  Highly Efficient and Robust Enantioselective Liquid-Liquid Extraction of 1,2-Amino Alcohols utilizing VAPOL- and VANOL-based Phosphoric Acid Hosts‏ ‎‡9  1‏
919 ‎‡a  highlyefficientenantioselectiveliquidliquidextractionof12aminoalcoholsusingspinolbasedphosphoricacidhosts‏ ‎‡A  Highly efficient enantioselective liquid-liquid extraction of 1,2-amino-alcohols using SPINOL based phosphoric acid hosts‏ ‎‡9  1‏
919 ‎‡a  highlyenantioselectiveconjugateadditionsofpotassiumorganotrifluoroboratestoenonesbyuseofmonodentatephosphoramiditeligands‏ ‎‡A  Highly enantioselective conjugate additions of potassium organotrifluoroborates to enones by use of monodentate phosphoramidite ligands‏ ‎‡9  1‏
919 ‎‡a  highlyenantioselectiverhodiumcatalyzedhydrogenationwithmonodentateligands‏ ‎‡A  Highly Enantioselective Rhodium-Catalyzed Hydrogenation with Monodentate Ligands‏ ‎‡9  1‏
919 ‎‡a  hydrationofnitrilesusingametalligandcooperativerutheniumpincercatalyst‏ ‎‡A  Hydration of nitriles using a metal-ligand cooperative ruthenium pincer catalyst‏ ‎‡9  1‏
919 ‎‡a  hydrogenationofpolyesterstopolyetherpolyols‏ ‎‡A  Hydrogenation of Polyesters to Polyether Polyols‏ ‎‡9  1‏
919 ‎‡a  hydroxymethylfurfuralaversatileplatformchemicalmadefromrenewableresources‏ ‎‡A  Hydroxymethylfurfural, a versatile platform chemical made from renewable resources.‏ ‎‡9  1‏
919 ‎‡a  improvementinthepalladiumcatalyzedmiyauraborylationreactionbyoptimizationofthebasescopeandmechanisticstudy‏ ‎‡A  Improvement in the Palladium-Catalyzed Miyaura Borylation Reaction by Optimization of the Base: Scope and Mechanistic Study‏ ‎‡9  1‏
919 ‎‡a  iridiummonodentatephosphoramiditecatalyzedasymmetrichydrogenationofnarylimines‏ ‎‡A  Iridium/monodentate phosphoramidite catalyzed asymmetric hydrogenation of N-aryl imines.‏ ‎‡9  1‏
919 ‎‡a  isomerizationofallylicalcoholstoketonescatalyzedbywelldefinedironpnppincercatalysts‏ ‎‡A  Isomerization of Allylic Alcohols to Ketones Catalyzed by Well-Defined Iron PNP Pincer Catalysts.‏ ‎‡9  1‏
919 ‎‡a  manganesepnppincercatalyzedisomerizationofallylichomoallylicalcoholstoketonesactivityselectivityefficiency‏ ‎‡A  Manganese PNP-pincer catalyzed isomerization of allylic/homo-allylic alcohols to ketones – activity, selectivity, efficiency‏ ‎‡9  1‏
919 ‎‡a  metaltriflatesfortheproductionofaromaticsfromlignin‏ ‎‡A  Metal Triflates for the Production of Aromatics from Lignin.‏ ‎‡9  1‏
919 ‎‡a  nylonintermediatesfrombiobasedlevulinicacid‏ ‎‡A  Nylon Intermediates from Bio-Based Levulinic Acid‏ ‎‡9  1‏
919 ‎‡a  catalyticapproachestomonomersforpolymersbasedonrenewables‏ ‎‡A  Catalytic Approaches to Monomers for Polymers Based on Renewables‏ ‎‡9  1‏
919 ‎‡a  caprolactamfromrenewableresourcescatalyticconversionof5hydroxymethylfurfuralintocaprolactone‏ ‎‡A  Caprolactam from Renewable Resources: Catalytic Conversion of 5-Hydroxymethylfurfural into Caprolactone‏ ‎‡9  1‏
919 ‎‡a  biobasedbuildingblocksfrom5hydroxymethylfurfuralvia1hydroxyhexane25dioneasintermediate‏ ‎‡A  Bio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediate‏ ‎‡9  1‏
919 ‎‡a  basefreeironcatalyzedtransferhydrogenationofestersusingetohashydrogensource‏ ‎‡A  Base-Free Iron Catalyzed Transfer Hydrogenation of Esters Using EtOH as Hydrogen Source‏ ‎‡9  1‏
919 ‎‡a  atthefrontierbetweenheterogeneousandhomogeneouscatalysishydrogenationofolefinsandalkyneswithsolubleironnanoparticles‏ ‎‡A  At the frontier between heterogeneous and homogeneous catalysis: hydrogenation of olefins and alkynes with soluble iron nanoparticles.‏ ‎‡9  1‏
919 ‎‡a  asymmetrichydrogenationusingmonodentatephosphoramiditeligands‏ ‎‡A  Asymmetric hydrogenation using monodentate phosphoramidite ligands‏ ‎‡9  1‏
919 ‎‡a  asymmetrichydrogenationof3substitutedpyridiniumsalts‏ ‎‡A  Asymmetric Hydrogenation of 3-Substituted Pyridinium Salts‏ ‎‡9  1‏
919 ‎‡a  aromaticmonomersbyinsituconversionofreactiveintermediatesintheacidcatalyzeddepolymerizationoflignin‏ ‎‡A  Aromatic monomers by in situ conversion of reactive intermediates in the acid-catalyzed depolymerization of lignin.‏ ‎‡9  1‏
919 ‎‡a  alkeneisomerisationcatalysedbyarutheniumpnnpincercomplex‏ ‎‡A  Alkene isomerisation catalysed by a ruthenium PNN pincer complex‏ ‎‡9  1‏
919 ‎‡a  advancedmodelcompoundsforunderstandingacidcatalyzedlignindepolymerizationidentificationofrenewablearomaticsandaligninderivedsolvent‏ ‎‡A  Advanced Model Compounds for Understanding Acid-Catalyzed Lignin Depolymerization: Identification of Renewable Aromatics and a Lignin-Derived Solvent‏ ‎‡9  1‏
919 ‎‡a  oxamichaeladditiontoαβunsaturatednitrilesanexpedientroutetoγaminoalcoholsandderivatives‏ ‎‡A  Oxa-Michael Addition to α,β-Unsaturated Nitriles: An Expedient Route to γ-Amino Alcohols and Derivatives‏ ‎‡9  1‏
919 ‎‡a  palladium0nhccatalyzedreductiveheckreactionofenonesadetailedmechanisticstudy‏ ‎‡A  Palladium(0)/NHC-Catalyzed Reductive Heck Reaction of Enones: A Detailed Mechanistic Study‏ ‎‡9  1‏
919 ‎‡a  palladiumcatalyzedasymmetricquaternarystereocenterformation‏ ‎‡A  Palladium-catalyzed asymmetric quaternary stereocenter formation‏ ‎‡9  1‏
919 ‎‡a  pdnhccatalyzedconjugateadditionversusthemizorokiheckreaction‏ ‎‡A  Pd-NHC catalyzed conjugate addition versus the Mizoroki-Heck reaction‏ ‎‡9  1‏
919 ‎‡a  pipphosandmorfphosprivilegedmonodentatephosphoramiditeligandsforrhodiumcatalyzedasymmetrichydrogenation‏ ‎‡A  PipPhos and MorfPhos: privileged monodentate phosphoramidite ligands for rhodium-catalyzed asymmetric hydrogenation‏ ‎‡9  1‏
919 ‎‡a  platinumcatalyzedselectivehydrationofhinderednitrilesandnitrileswithacidorbasesensitivegroups‏ ‎‡A  Platinum-catalyzed selective hydration of hindered nitriles and nitriles with acid- or base-sensitive groups‏ ‎‡9  1‏
919 ‎‡a  propertiesofnovelpolyestersmadefromrenewable14pentanediol‏ ‎‡A  Properties of Novel Polyesters Made from Renewable 1,4-Pentanediol‏ ‎‡9  1‏
919 ‎‡a  rheniumcatalyzeddeoxydehydrationofrenewabletriolsderivedfromsugars‏ ‎‡A  Rhenium-catalyzed deoxydehydration of renewable triols derived from sugars‏ ‎‡9  1‏
919 ‎‡a  selectivebasefreetransferhydrogenationofαβunsaturatedcarbonylcompoundsusingiprohoretohashydrogensource‏ ‎‡A  Selective Base-free Transfer Hydrogenation of α,β-Unsaturated Carbonyl Compounds using iPrOH or EtOH as Hydrogen Source.‏ ‎‡9  1‏
919 ‎‡a  selectiveconversionofpolyenestomonoenesbyrucl3catalyzedtransferhydrogenationthecaseofcashewnutshellliquid‏ ‎‡A  Selective conversion of polyenes to monoenes by RuCl(3) -catalyzed transfer hydrogenation: the case of cashew nutshell liquid‏ ‎‡9  1‏
919 ‎‡a  additivefreeisomerizationofallylicalcoholstoketoneswithacobaltpnppincercatalyst‏ ‎‡A  Additive-Free Isomerization of Allylic Alcohols to Ketones with a Cobalt PNP Pincer Catalyst‏ ‎‡9  1‏
919 ‎‡a  synthesisofαketoaldehydes1via1selectivecuscp1scpcatalyzedoxidationofαhydroxyketones‏ ‎‡A  Synthesis of α-keto aldehydes <i>via</i> selective Cu(<scp>i</scp>)-catalyzed oxidation of α-hydroxy ketones‏ ‎‡9  1‏
919 ‎‡a  unravellingthereactionpathofrhodiummonophoscatalysedolefinhydrogenation‏ ‎‡A  Unravelling the reaction path of rhodium-MonoPhos-catalysed olefin hydrogenation‏ ‎‡9  1‏
919 ‎‡a  synthesisofsolutionphasephosphoramiditeandphosphiteligandlibrariesandtheirinsituscreeningintherhodiumcatalyzedasymmetricadditionofarylboronicacids‏ ‎‡A  Synthesis of solution-phase phosphoramidite and phosphite ligand libraries and their in situ screening in the rhodium-catalyzed asymmetric addition of arylboronic acids‏ ‎‡9  1‏
919 ‎‡a  synthesisofrenewablefinechemicalbuildingblocksbyreductivecouplingbetweenfurfuralderivativesandterpenes‏ ‎‡A  Synthesis of renewable fine-chemical building blocks by reductive coupling between furfural derivatives and terpenes‏ ‎‡9  1‏
919 ‎‡a  synthesisof1n1substituted3hydroxypyridiniumsaltsfrombioderived5hydroxymethylfurfuralinwater‏ ‎‡A  Synthesis of <i>N</i>-Substituted 3-Hydroxypyridinium Salts from Bioderived 5-Hydroxymethylfurfural in Water‏ ‎‡9  1‏
919 ‎‡a  synthesischaracterizationandcatalyticactivityofnovelrutheniumcomplexesbearingnnnclickbasedligands‏ ‎‡A  Synthesis, characterization and catalytic activity of novel ruthenium complexes bearing NNN click based ligands‏ ‎‡9  1‏
919 ‎‡a  synthesisandapplicationinasymmetric100100bondformationofsolutionphaseligandlibrariesofmonodentatephosphoramidites‏ ‎‡A  Synthesis and application in asymmetric C-C bond formation of solution phase ligand libraries of monodentate phosphoramidites‏ ‎‡9  1‏
919 ‎‡a  selectivehydrogenationofαβunsaturatedaldehydesandketonesbyairstablerutheniumnnscomplexes‏ ‎‡A  Selective Hydrogenation of α,β-Unsaturated Aldehydes and Ketones by Air-Stable Ruthenium NNS Complexes‏ ‎‡9  1‏
919 ‎‡a  achiralligandsdramaticallyenhancerateandenantioselectivityintherhphosphoramiditecatalyzedhydrogenationofalphabetadisubstitutedunsaturatedacids‏ ‎‡A  Achiral ligands dramatically enhance rate and enantioselectivity in the Rh/phosphoramidite-catalyzed hydrogenation of alpha,beta-disubstituted unsaturated acids‏ ‎‡9  1‏
919 ‎‡a  simpleandeffectivecocatalystforringclosingenynemetathesisusinggrubbs1typecatalystsapracticalalternativetomorisconditions‏ ‎‡A  A Simple and Effective Co-Catalyst for Ring-Closing Enyne Metathesis Using Grubbs I type Catalysts: A Practical Alternative to “Mori’s Conditions”‏ ‎‡9  1‏
919 ‎‡a  metalligandcooperativepathwayforintermolecularoxamichaeladditionstounsaturatednitriles‏ ‎‡A  A metal-ligand cooperative pathway for intermolecular oxa-Michael additions to unsaturated nitriles‏ ‎‡9  1‏
919 ‎‡a  33diarylbinolphosphoricacidsasenantioselectiveextractantsofbenzylicprimaryamines‏ ‎‡A  3,3'-Diaryl-BINOL phosphoric acids as enantioselective extractants of benzylic primary amines‏ ‎‡9  1‏
919 ‎‡a  catalyticregioselectiveoxidationofglycosides‏ ‎‡A  Catalytic regioselective oxidation of glycosides‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
947 ‎‡a  NL‏ ‎‡9  1‏
996 ‎‡2  ISNI|0000000388713293‏
996 ‎‡2  NTA|172481287‏
996 ‎‡2  NTA|072909587‏
996 ‎‡2  LC|n 85048682‏
996 ‎‡2  ISNI|0000000047733069‏
996 ‎‡2  ISNI|0000000042872967‏
996 ‎‡2  RERO|A000048700‏
996 ‎‡2  LC|no 95046915‏
996 ‎‡2  NTA|094968950‏
996 ‎‡2  RERO|A000048708‏
996 ‎‡2  ISNI|000000004550529X‏
996 ‎‡2  BIBSYS|99059899‏
996 ‎‡2  J9U|987007318004905171‏
996 ‎‡2  LIH|LNB:BN_c_U;=B_e_‏
996 ‎‡2  NTA|304019194‏
996 ‎‡2  DNB|1030592608‏
996 ‎‡2  ISNI|0000000387554657‏
996 ‎‡2  ISNI|0000000389455388‏
996 ‎‡2  ISNI|0000000390085935‏
996 ‎‡2  ISNI|0000000039739663‏
996 ‎‡2  LC|no2002063071‏
996 ‎‡2  NTA|073818208‏
996 ‎‡2  NTA|303260998‏
996 ‎‡2  NTA|069360960‏
996 ‎‡2  NTA|289031621‏
996 ‎‡2  NUKAT|n 95205589‏
996 ‎‡2  ISNI|000000039277737X‏
996 ‎‡2  NTA|124850391‏
996 ‎‡2  NTA|42104991X‏
996 ‎‡2  NTA|137146779‏
996 ‎‡2  NTA|068986475‏
996 ‎‡2  ISNI|0000000394273351‏
996 ‎‡2  NTA|18040069X‏
996 ‎‡2  RERO|A000048706‏
996 ‎‡2  NTA|086423215‏
996 ‎‡2  ISNI|0000000371289561‏
996 ‎‡2  ISNI|0000000043956636‏
996 ‎‡2  NTA|091729211‏
996 ‎‡2  ISNI|0000000389764244‏
996 ‎‡2  SUDOC|194289494‏
996 ‎‡2  DNB|115774219X‏
996 ‎‡2  ISNI|0000000392437041‏
996 ‎‡2  LC|n 81139131‏
996 ‎‡2  ISNI|0000000393840262‏
996 ‎‡2  NTA|073461504‏
996 ‎‡2  NTA|260070327‏
996 ‎‡2  SUDOC|111806305‏
996 ‎‡2  PLWABN|9810618464005606‏
996 ‎‡2  NTA|261614916‏
996 ‎‡2  CAOONL|ncf11400049‏
996 ‎‡2  RERO|A012885615‏
996 ‎‡2  NTA|090835948‏
996 ‎‡2  ISNI|0000000393955684‏
996 ‎‡2  NTA|408671564‏
996 ‎‡2  NTA|069417490‏
996 ‎‡2  NTA|439438640‏
996 ‎‡2  ISNI|0000000395906085‏
996 ‎‡2  ISNI|0000000392868511‏
996 ‎‡2  NTA|075055961‏
996 ‎‡2  NTA|073364495‏
996 ‎‡2  ISNI|0000000390765543‏
996 ‎‡2  SUDOC|076185699‏
996 ‎‡2  ISNI|0000000392491566‏
996 ‎‡2  NTA|304080799‏
996 ‎‡2  LC|n 80064129‏
996 ‎‡2  ISNI|0000000396278383‏
996 ‎‡2  SUDOC|17504158X‏
996 ‎‡2  ISNI|0000000022277466‏
996 ‎‡2  ISNI|0000000393358353‏
996 ‎‡2  NTA|180520725‏
996 ‎‡2  ISNI|0000000387983849‏
996 ‎‡2  NUKAT|n 00030494‏
996 ‎‡2  ISNI|0000000389690329‏
996 ‎‡2  NTA|162056419‏
996 ‎‡2  NKC|mub20201064281‏
996 ‎‡2  NTA|290264367‏
996 ‎‡2  NTA|072819367‏
996 ‎‡2  ISNI|0000000395947063‏
996 ‎‡2  NTA|067800351‏
996 ‎‡2  ISNI|0000000390202302‏
996 ‎‡2  BIBSYS|90291236‏
996 ‎‡2  NTA|105170399‏
996 ‎‡2  ISNI|0000000389645608‏
996 ‎‡2  NTA|073730378‏
996 ‎‡2  ISNI|0000000394294531‏
996 ‎‡2  NTA|072374349‏
996 ‎‡2  NTA|124547044‏
996 ‎‡2  ISNI|0000000057383162‏
996 ‎‡2  NTA|305472666‏
996 ‎‡2  NDL|00725769‏
996 ‎‡2  SUDOC|119647710‏
996 ‎‡2  NTA|341039241‏
996 ‎‡2  LC|no2003106107‏
996 ‎‡2  NTA|124519466‏
996 ‎‡2  NTA|124491154‏
996 ‎‡2  VLACC|000037973‏
996 ‎‡2  NTA|124036740‏
996 ‎‡2  NTA|09650577X‏
996 ‎‡2  NTA|133404692‏
996 ‎‡2  SUDOC|24477871X‏
996 ‎‡2  ISNI|0000000368744690‏
996 ‎‡2  NTA|124518214‏
996 ‎‡2  ISNI|0000000387354655‏
996 ‎‡2  NTA|241859913‏
996 ‎‡2  ISNI|0000000033649579‏
996 ‎‡2  NTA|151277214‏
996 ‎‡2  ISNI|0000000388909691‏
996 ‎‡2  NTA|130653330‏
996 ‎‡2  NTA|161389562‏
996 ‎‡2  NTA|203183592‏
996 ‎‡2  NTA|296198684‏
996 ‎‡2  LC|n 84805090‏
996 ‎‡2  ISNI|0000000391432345‏
996 ‎‡2  ISNI|0000000396755952‏
996 ‎‡2  BIBSYS|4056793‏
996 ‎‡2  NTA|096172975‏
996 ‎‡2  NTA|074656341‏
996 ‎‡2  ISNI|0000000374533769‏
996 ‎‡2  NTA|074772643‏
996 ‎‡2  NTA|241860288‏
996 ‎‡2  NTA|343275872‏
996 ‎‡2  LC|n 2015039494‏
996 ‎‡2  NTA|157613313‏
996 ‎‡2  NSK|000692885‏
996 ‎‡2  ISNI|000000039130364X‏
996 ‎‡2  NTA|07300930X‏
996 ‎‡2  NTA|419926097‏
996 ‎‡2  NTA|079162533‏
996 ‎‡2  BIBSYS|90587337‏
996 ‎‡2  BIBSYS|90634087‏
996 ‎‡2  ISNI|0000000396962783‏
996 ‎‡2  ISNI|0000000393591972‏
996 ‎‡2  ISNI|0000000041115585‏
996 ‎‡2  ISNI|0000000042965418‏
996 ‎‡2  ISNI|000000038926600X‏
996 ‎‡2  ISNI|0000000394125287‏
996 ‎‡2  LC|n 94066932‏
996 ‎‡2  NTA|142907294‏
996 ‎‡2  NTA|320764109‏
996 ‎‡2  NTA|073252158‏
996 ‎‡2  NTA|067848702‏
996 ‎‡2  ISNI|0000000391270526‏
996 ‎‡2  ISNI|0000000393660501‏
996 ‎‡2  BIBSYS|1592544501198‏
996 ‎‡2  NTA|073520470‏
996 ‎‡2  ISNI|0000000388895584‏
996 ‎‡2  NTA|072790903‏
996 ‎‡2  ISNI|0000000393187961‏
996 ‎‡2  NTA|110638867‏
996 ‎‡2  NTA|101358334‏
996 ‎‡2  LC|n 80112453‏
996 ‎‡2  ISNI|0000000393682786‏
996 ‎‡2  NTA|075055856‏
996 ‎‡2  BIBSYS|90288352‏
996 ‎‡2  NTA|073293970‏
996 ‎‡2  LC|no 92021071‏
996 ‎‡2  LC|n 95049762‏
996 ‎‡2  BIBSYS|5080590‏
996 ‎‡2  NTA|067809200‏
996 ‎‡2  ISNI|0000000390681913‏
996 ‎‡2  CAOONL|ncf11609047‏
996 ‎‡2  NTA|240915240‏
996 ‎‡2  SUDOC|204773512‏
996 ‎‡2  NTA|420692525‏
996 ‎‡2  ISNI|0000000392608875‏
996 ‎‡2  ISNI|000000036892339X‏
996 ‎‡2  ISNI|0000000387470031‏
996 ‎‡2  LC|n 93011375‏
996 ‎‡2  ISNI|0000000024811140‏
996 ‎‡2  SUDOC|166018473‏
996 ‎‡2  ISNI|0000000089993504‏
996 ‎‡2  ISNI|0000000115919640‏
996 ‎‡2  BNF|12267998‏
996 ‎‡2  BNF|13186905‏
996 ‎‡2  ISNI|0000000389173102‏
996 ‎‡2  NTA|071133518‏
996 ‎‡2  NTA|17321942X‏
996 ‎‡2  ISNI|0000000388101035‏
996 ‎‡2  NTA|161395244‏
996 ‎‡2  SIMACOB|57076067‏
996 ‎‡2  NTA|069274533‏
996 ‎‡2  ISNI|0000000080048047‏
996 ‎‡2  ISNI|000000038705306X‏
996 ‎‡2  ISNI|0000000396523115‏
996 ‎‡2  DNB|1158976453‏
996 ‎‡2  NTA|243911076‏
996 ‎‡2  NTA|392619288‏
996 ‎‡2  NTA|411431617‏
996 ‎‡2  NTA|244037612‏
996 ‎‡2  RERO|A003161349‏
996 ‎‡2  RERO|A003161348‏
996 ‎‡2  NTA|298210436‏
996 ‎‡2  J9U|987007455480505171‏
996 ‎‡2  RERO|A003161347‏
996 ‎‡2  ISNI|0000000389058585‏
996 ‎‡2  ISNI|0000000387940849‏
996 ‎‡2  NTA|093674392‏
996 ‎‡2  NTA|306279975‏
996 ‎‡2  LC|n 96009217‏
996 ‎‡2  NTA|069142424‏
996 ‎‡2  NTA|329230573‏
996 ‎‡2  J9U|987007350983705171‏
996 ‎‡2  ISNI|0000000395175630‏
996 ‎‡2  NTA|067829325‏
996 ‎‡2  NTA|075279770‏
996 ‎‡2  NTA|115278575‏
996 ‎‡2  DNB|12736739X‏
996 ‎‡2  ISNI|0000000041257110‏
996 ‎‡2  NTA|443313776‏
996 ‎‡2  NKC|jo2015883724‏
996 ‎‡2  LC|n 82230009‏
996 ‎‡2  NTA|434281409‏
996 ‎‡2  NTA|241860253‏
996 ‎‡2  LC|n 82210034‏
996 ‎‡2  NTA|356388425‏
996 ‎‡2  NTA|073514454‏
996 ‎‡2  LC|no2004099212‏
996 ‎‡2  ISNI|0000000033905923‏
996 ‎‡2  ISNI|0000000393465298‏
996 ‎‡2  NTA|241859921‏
996 ‎‡2  NTA|289021944‏
996 ‎‡2  NTA|243911106‏
996 ‎‡2  J9U|987007345415705171‏
996 ‎‡2  NTA|252229878‏
996 ‎‡2  ISNI|0000000459452730‏
996 ‎‡2  ISNI|000000038950897X‏
996 ‎‡2  NUKAT|n 2018145760‏
996 ‎‡2  LC|n 82250904‏
996 ‎‡2  ISNI|0000000391924331‏
996 ‎‡2  ISNI|0000000394487763‏
996 ‎‡2  ISNI|0000000387812679‏
996 ‎‡2  ISNI|0000000387104584‏
996 ‎‡2  ISNI|0000000395252026‏
996 ‎‡2  NII|DA03445433‏
996 ‎‡2  ISNI|000000038467395X‏
996 ‎‡2  SUDOC|178436615‏
996 ‎‡2  ISNI|0000000397950362‏
996 ‎‡2  ISNI|0000000383491230‏
996 ‎‡2  ISNI|0000000397145611‏
996 ‎‡2  ISNI|0000000395715289‏
996 ‎‡2  LC|nr 94033184‏
996 ‎‡2  LC|n 82013229‏
996 ‎‡2  J9U|987007327257205171‏
996 ‎‡2  ISNI|0000000423106625‏
996 ‎‡2  NTA|250198967‏
996 ‎‡2  NTA|296472050‏
996 ‎‡2  NTA|070235341‏
996 ‎‡2  LC|no2023018203‏
996 ‎‡2  NTA|074702386‏
996 ‎‡2  NTA|073574147‏
997 ‎‡a  1951 0 lived 0000 0‏ ‎‡9  1‏
998 ‎‡a  Vries, Johannes G. de.‏ ‎‡2  NUKAT|n 2007089212‏ ‎‡3  suggested‏ ‎‡3  viafid‏
998 ‎‡a  Vries, Johannes G. de‏ ‎‡2  J9U|987008729564805171‏ ‎‡3  suggested‏
998 ‎‡a  Vries, Johannes G. ˜deœ‏ ‎‡2  DNB|132252880‏ ‎‡3  suggested‏ ‎‡3  title: (0.65, 'isomerizationofallylicalcoholstotheketonescatalyzedby1rowtransitionmetalpincercomplexes', 'isomerizationofallylicalcoholstoketonescatalyzedbywelldefinedironpnppincercatalysts')‏
998 ‎‡a  Vries, Johannes G. de‏ ‎‡q  (Johannes Gerardus de)‏ ‎‡2  RERO|A013188309‏ ‎‡3  title: (0.74, 'stereoselectivesynthesis', 'enantioanddiastereoselectivesynthesisofγaminoalcohols')‏
998 ‎‡a  Vries, Johannes Gerardus de,‏ ‎‡2  NKC|mub20201064281‏ ‎‡3  suggested‏
998 ‎‡a  Vries, Johannes G. de‏ ‎‡2  SUDOC|111806305‏ ‎‡3  suggested‏
998 ‎‡a  Vries, Johannes G. de‏ ‎‡2  ISNI|0000000115919640‏ ‎‡3  suggested‏
998 ‎‡a  DE VRIES, Johannes Gerardus‏ ‎‡2  ISNI|0000000115919640‏ ‎‡3  suggested‏
998 ‎‡a  Vries, Johannes Gerardus de‏ ‎‡2  ISNI|0000000115919640‏ ‎‡3  suggested‏
998 ‎‡a  de Vries, J.G.‏ ‎‡2  ISNI|0000000115919640‏ ‎‡3  suggested‏
998 ‎‡a  Vries, Johannes G. de‏ ‎‡2  ISNI|0000000115919640‏ ‎‡3  suggested‏
998 ‎‡a  de Vries, J.G.‏ ‎‡2  BIBSYS|12028361‏ ‎‡3  viafid‏
998 ‎‡a  Vries, Johannes G. de‏ ‎‡2  LC|nb2006025538‏ ‎‡3  title: (0.74, 'stereoselectivesynthesis', 'enantioanddiastereoselectivesynthesisofγaminoalcohols')‏