VIAF

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Leader     00000nz a2200037n 45 0
001     WKP|Q98211807  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241020233206.0
008     241020nneanz||abbn n and d
035 ‎‡a  (WKP)Q98211807‏
024 ‎‡a  0000-0002-3998-185X‏ ‎‡2  orcid‏
035 ‎‡a  (OCoLC)Q98211807‏
100 0 ‎‡a  José L Jiménez‏ ‎‡c  researcher‏ ‎‡9  en‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  José L Jiménez‏ ‎‡c  onderzoeker‏ ‎‡9  nl‏
670 ‎‡a  Author's 1,3-dipolar cycloaddition of 2-dialkylaminothioisomünchnones with aliphatic aldehydes: synthesis of beta-lactams and thiiranes, structure elucidation, and rationale for chemoselective fragmentation of cycloadducts‏
670 ‎‡a  Author's A family of hydrogels based on ureido-linked aminopolyol-derived amphiphiles and bolaamphiphiles: synthesis, gelation under thermal and sonochemical stimuli, and mesomorphic characterization.‏
670 ‎‡a  Author's A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen‏
670 ‎‡a  Author's A new model for mapping the peptide backbone: predicting proton chemical shifts in proteins.‏
670 ‎‡a  Author's A new synthesis of 6-oxopyrimidinium-4-olates. Theoretical study of the regioselective cycloaddition of arylisocyanates with A 1,3-thiazolium-4-olate system‏
670 ‎‡a  Author's A quantitative structure-reactivity relationship in N-acetyl oxazolidines: an electrostatic interaction controls rotamer population‏
670 ‎‡a  Author's Absolute Asymmetric Synthesis under Physical Fields: Facts and Fictions‏
670 ‎‡a  Author's Assessing the whole range of CuAAC mechanisms by DFT calculations--on the intermediacy of copper acetylides.‏
670 ‎‡a  Author's Chiral N-acyloxazolidines: synthesis, structure, and mechanistic insights‏
670 ‎‡a  Author's Computational Screening of New Orthogonal Metal-Free Dipolar Cycloadditions of Mesomeric Betaines.‏
670 ‎‡a  Author's Conformation of secondary amides. A predictive algorithm that correlates DFT-calculated structures and experimental proton chemical shifts.‏
670 ‎‡a  Author's Cycloaddition Chemistry of 1,3-Thiazolium-4-olate Systems. Reaction with Nitroalkenes and Interpretation of Results Using PM3 Calculations‏
670 ‎‡a  Author's Diastereoselective Cycloadditions of Nitroalkenes as an Approach to the Assembly of Bicyclic Nitrogen Heterocycles‏
670 ‎‡a  Author's Dissecting competitive mechanisms: thionation vs. cycloaddition in the reaction of thioisomunchnones with isothiocyanates under microwave irradiation.‏
670 ‎‡a  Author's Experimental and theoretical insights regarding the cycloaddition reaction of carbohydrate-based 1,2-diaza-1,3-butadienes and acrylonitrile. A model case for the behavior of chiral azoalkenes and unsymmetric olefins.‏
670 ‎‡a  Author's Exploiting synthetic chemistry with mesoionic rings: improvements achieved with thioisomünchnones‏
670 ‎‡a  Author's Greener media in chemical synthesis and processing‏
670 ‎‡a  Author's Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions‏
670 ‎‡a  Author's Münchnone-Alkene Cycloadditions: Deviations from the FMO Theory. Theoretical Studies in the Search of the Transition State‏
670 ‎‡a  Author's Novel acid-catalyzed rearrangement of tetrahydro-1,2,3,4-tetrazines: unexpected formation of glycosazones‏
670 ‎‡a  Author's On the dual reactivity of a Janus-type mesoionic dipole: experiments and theoretical validation‏
670 ‎‡a  Author's On the enhanced reactivity and selectivity of triazole formation in molecular flasks. A theoretical rationale‏
670 ‎‡a  Author's On the Plausibility of Pseudosugar Formation in Cometary Ices and Oxygen-rich Tholins‏
670 ‎‡a  Author's On the prebiotic synthesis of D-sugars catalyzed by L-peptides: assessments from first-principles calculations.‏
670 ‎‡a  Author's Prebiotic-Like Condensations of Cyanamide and Glyoxal: Revisiting Intractable Biotars‏
670 ‎‡a  Author's Pseudo-cyclic structures of mono- and di-azaderivatives of malondialdehydes. Synthesis and conformational disentanglement by computational analyses‏
670 ‎‡a  Author's Push-pull 1,3-thiazolium-5-thiolates. Formation via concerted and stepwise pathways, and theoretical evaluation of NLO properties.‏
670 ‎‡a  Author's Rethinking aromaticity in H-bonded systems. Caveats for transition structures involving hydrogen transfer and π-delocalization‏
670 ‎‡a  Author's Schiff bases from D-glucosamine and aliphatic ketones.‏
670 ‎‡a  Author's Stepwise cycloadditions of mesoionic systems: thionation of thioisomünchnones by isothiocyanates‏
670 ‎‡a  Author's Stepwise formation of 1,3-diazolium-4-thiolates by münchnone cycloadditions: promising candidates for nonlinear optics‏
670 ‎‡a  Author's Substrate-Controlled Stereodifferentiation of Tandem [4 + 2]/[3 + 2] Cycloadditions by a Vicinal Carbohydrate-Based Template‏
670 ‎‡a  Author's Symmetry breaking by spontaneous crystallization--is it the most plausible source of terrestrial handedness we have long been looking for?--A reappraisal‏
670 ‎‡a  Author's Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state‏
670 ‎‡a  Author's Thermal and sonochemical studies on the Diels-Alder cycloadditions of masked o-benzoquinones with furans: new insights into the reaction mechanism‏
670 ‎‡a  Author's Thionation of mesoionics with isothiocyanates: evidence supporting a four-step domino process and ruling out a [2 + 2] mechanism.‏
670 ‎‡a  Author's Unusual aryl migration in a mesomeric betaine in the solid and liquid state: mechanistic insights into the SNAr reaction‏
670 ‎‡a  Author's What does elementary chirality have to do with neutrinos?‏
909 ‎‡a  (orcid) 000000023998185x‏ ‎‡9  1‏
919 ‎‡a  chiralnacyloxazolidinessynthesisstructureandmechanisticinsights‏ ‎‡A  Chiral N-acyloxazolidines: synthesis, structure, and mechanistic insights‏ ‎‡9  1‏
919 ‎‡a  assessingthewholerangeofcuaacmechanismsbydftcalculationsontheintermediacyofcopperacetylides‏ ‎‡A  Assessing the whole range of CuAAC mechanisms by DFT calculations--on the intermediacy of copper acetylides.‏ ‎‡9  1‏
919 ‎‡a  ontheplausibilityofpseudosugarformationincometaryicesandoxygenrichtholins‏ ‎‡A  On the Plausibility of Pseudosugar Formation in Cometary Ices and Oxygen-rich Tholins‏ ‎‡9  1‏
919 ‎‡a  conformationofsecondaryamidesapredictivealgorithmthatcorrelatesdftcalculatedstructuresandexperimentalprotonchemicalshifts‏ ‎‡A  Conformation of secondary amides. A predictive algorithm that correlates DFT-calculated structures and experimental proton chemical shifts.‏ ‎‡9  1‏
919 ‎‡a  pushpull13thiazolium5thiolatesformationviaconcertedandstepwisepathwaysandtheoreticalevaluationofnloproperties‏ ‎‡A  Push-pull 1,3-thiazolium-5-thiolates. Formation via concerted and stepwise pathways, and theoretical evaluation of NLO properties.‏ ‎‡9  1‏
919 ‎‡a  ontheenhancedreactivityandselectivityoftriazoleformationinmolecularflasksatheoreticalrationale‏ ‎‡A  On the enhanced reactivity and selectivity of triazole formation in molecular flasks. A theoretical rationale‏ ‎‡9  1‏
919 ‎‡a  schiffbasesfrom500glucosamineandaliphaticketones‏ ‎‡A  Schiff bases from D-glucosamine and aliphatic ketones.‏ ‎‡9  1‏
919 ‎‡a  stepwisecycloadditionsofmesoionicsystemsthionationofthioisomunchnonesbyisothiocyanates‏ ‎‡A  Stepwise cycloadditions of mesoionic systems: thionation of thioisomünchnones by isothiocyanates‏ ‎‡9  1‏
919 ‎‡a  stepwiseformationof13diazolium4thiolatesbymunchnonecycloadditionspromisingcandidatesfornonlinearoptics‏ ‎‡A  Stepwise formation of 1,3-diazolium-4-thiolates by münchnone cycloadditions: promising candidates for nonlinear optics‏ ‎‡9  1‏
919 ‎‡a  onthedualreactivityofajanustypemesoionicdipoleexperimentsandtheoreticalvalidation‏ ‎‡A  On the dual reactivity of a Janus-type mesoionic dipole: experiments and theoretical validation‏ ‎‡9  1‏
919 ‎‡a  novelacidcatalyzedrearrangementoftetrahydro1234tetrazinesunexpectedformationofglycosazones‏ ‎‡A  Novel acid-catalyzed rearrangement of tetrahydro-1,2,3,4-tetrazines: unexpected formation of glycosazones‏ ‎‡9  1‏
919 ‎‡a  substratecontrolledstereodifferentiationoftandemcycloadditionsbyavicinalcarbohydratebasedtemplate‏ ‎‡A  Substrate-Controlled Stereodifferentiation of Tandem [4 + 2]/[3 + 2] Cycloadditions by a Vicinal Carbohydrate-Based Template‏ ‎‡9  1‏
919 ‎‡a  ontheprebioticsynthesisof500sugarscatalyzedby50peptidesassessmentsfrom1principlescalculations‏ ‎‡A  On the prebiotic synthesis of D-sugars catalyzed by L-peptides: assessments from first-principles calculations.‏ ‎‡9  1‏
919 ‎‡a  cycloadditionchemistryof13thiazolium4olatesystemsreactionwithnitroalkenesandinterpretationofresultsusingpm3calculations‏ ‎‡A  Cycloaddition Chemistry of 1,3-Thiazolium-4-olate Systems. Reaction with Nitroalkenes and Interpretation of Results Using PM3 Calculations‏ ‎‡9  1‏
919 ‎‡a  absoluteasymmetricsynthesisunderphysicalfieldsfactsandfictions‏ ‎‡A  Absolute Asymmetric Synthesis under Physical Fields: Facts and Fictions‏ ‎‡9  1‏
919 ‎‡a  diastereoselectivecycloadditionsofnitroalkenesasanapproachtotheassemblyofbicyclicnitrogenheterocycles‏ ‎‡A  Diastereoselective Cycloadditions of Nitroalkenes as an Approach to the Assembly of Bicyclic Nitrogen Heterocycles‏ ‎‡9  1‏
919 ‎‡a  quantitativestructurereactivityrelationshipinnacetyloxazolidinesanelectrostaticinteractioncontrolsrotamerpopulation‏ ‎‡A  A quantitative structure-reactivity relationship in N-acetyl oxazolidines: an electrostatic interaction controls rotamer population‏ ‎‡9  1‏
919 ‎‡a  newsynthesisof6oxopyrimidinium4olatestheoreticalstudyoftheregioselectivecycloadditionofarylisocyanateswitha13thiazolium4olatesystem‏ ‎‡A  A new synthesis of 6-oxopyrimidinium-4-olates. Theoretical study of the regioselective cycloaddition of arylisocyanates with A 1,3-thiazolium-4-olate system‏ ‎‡9  1‏
919 ‎‡a  whatdoeselementarychiralityhavetodowithneutrinos‏ ‎‡A  What does elementary chirality have to do with neutrinos?‏ ‎‡9  1‏
919 ‎‡a  unusualarylmigrationinamesomericbetaineinthesolidandliquidstatemechanisticinsightsintothesnarreaction‏ ‎‡A  Unusual aryl migration in a mesomeric betaine in the solid and liquid state: mechanistic insights into the SNAr reaction‏ ‎‡9  1‏
919 ‎‡a  symmetrybreakingbyspontaneouscrystallizationisitthemostplausiblesourceofterrestrialhandednesswehavelongbeenlookingforareappraisal‏ ‎‡A  Symmetry breaking by spontaneous crystallization--is it the most plausible source of terrestrial handedness we have long been looking for?--A reappraisal‏ ‎‡9  1‏
919 ‎‡a  tautomerisminschiffbasesthecasesof2hydroxy1naphthaldehydeand1hydroxy2naphthaldehydeinvestigatedinsolutionandthesolidstate‏ ‎‡A  Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state‏ ‎‡9  1‏
919 ‎‡a  thermalandsonochemicalstudiesonthedielsaldercycloadditionsofmaskedobenzoquinoneswithfuransnewinsightsintothereactionmechanism‏ ‎‡A  Thermal and sonochemical studies on the Diels-Alder cycloadditions of masked o-benzoquinones with furans: new insights into the reaction mechanism‏ ‎‡9  1‏
919 ‎‡a  dissectingcompetitivemechanismsthionationvscycloadditioninthereactionofthioisomunchnoneswithisothiocyanatesundermicrowaveirradiation‏ ‎‡A  Dissecting competitive mechanisms: thionation vs. cycloaddition in the reaction of thioisomunchnones with isothiocyanates under microwave irradiation.‏ ‎‡9  1‏
919 ‎‡a  computationalscreeningofneworthogonalmetalfreedipolarcycloadditionsofmesomericbetaines‏ ‎‡A  Computational Screening of New Orthogonal Metal-Free Dipolar Cycloadditions of Mesomeric Betaines.‏ ‎‡9  1‏
919 ‎‡a  thionationofmesoionicswithisothiocyanatesevidencesupportinga4stepdominoprocessandrulingoutamechanism‏ ‎‡A  Thionation of mesoionics with isothiocyanates: evidence supporting a four-step domino process and ruling out a [2 + 2] mechanism.‏ ‎‡9  1‏
919 ‎‡a  prebioticlikecondensationsofcyanamideandglyoxalrevisitingintractablebiotars‏ ‎‡A  Prebiotic-Like Condensations of Cyanamide and Glyoxal: Revisiting Intractable Biotars‏ ‎‡9  1‏
919 ‎‡a  newmodelformappingthepeptidebackbonepredictingprotonchemicalshiftsinproteins‏ ‎‡A  A new model for mapping the peptide backbone: predicting proton chemical shifts in proteins.‏ ‎‡9  1‏
919 ‎‡a  pseudocyclicstructuresofmonoand501azaderivativesofmalondialdehydessynthesisandconformationaldisentanglementbycomputationalanalyses‏ ‎‡A  Pseudo-cyclic structures of mono- and di-azaderivatives of malondialdehydes. Synthesis and conformational disentanglement by computational analyses‏ ‎‡9  1‏
919 ‎‡a  exploitingsyntheticchemistrywithmesoionicringsimprovementsachievedwiththioisomunchnones‏ ‎‡A  Exploiting synthetic chemistry with mesoionic rings: improvements achieved with thioisomünchnones‏ ‎‡9  1‏
919 ‎‡a  munchnonealkenecycloadditionsdeviationsfromthefmotheorytheoreticalstudiesinthesearchofthetransitionstate‏ ‎‡A  Münchnone-Alkene Cycloadditions: Deviations from the FMO Theory. Theoretical Studies in the Search of the Transition State‏ ‎‡9  1‏
919 ‎‡a  13dipolarcycloadditionof2dialkylaminothioisomunchnoneswithaliphaticaldehydessynthesisofbetalactamsandthiiranesstructureelucidationandrationaleforchemoselectivefragmentationofcycloadducts‏ ‎‡A  1,3-dipolar cycloaddition of 2-dialkylaminothioisomünchnones with aliphatic aldehydes: synthesis of beta-lactams and thiiranes, structure elucidation, and rationale for chemoselective fragmentation of cycloadducts‏ ‎‡9  1‏
919 ‎‡a  mechanisticstudiesof13dipolarcycloadditionsofbicyclicthioisomunchnoneswithalkenesacomputationalrationalefocusedondonoracceptorinteractions‏ ‎‡A  Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions‏ ‎‡9  1‏
919 ‎‡a  experimentalandtheoreticalinsightsregardingthecycloadditionreactionofcarbohydratebased12diaza13butadienesandacrylonitrileamodelcaseforthebehaviorofchiralazoalkenesandunsymmetricolefins‏ ‎‡A  Experimental and theoretical insights regarding the cycloaddition reaction of carbohydrate-based 1,2-diaza-1,3-butadienes and acrylonitrile. A model case for the behavior of chiral azoalkenes and unsymmetric olefins.‏ ‎‡9  1‏
919 ‎‡a  familyofhydrogelsbasedonureidolinkedaminopolyolderivedamphiphilesandbolaamphiphilessynthesisgelationunderthermalandsonochemicalstimuliandmesomorphiccharacterization‏ ‎‡A  A family of hydrogels based on ureido-linked aminopolyol-derived amphiphiles and bolaamphiphiles: synthesis, gelation under thermal and sonochemical stimuli, and mesomorphic characterization.‏ ‎‡9  1‏
919 ‎‡a  fullydiastereoselectiveoxidationofamesoionicdipolewithtripletmolecularoxygen‏ ‎‡A  A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen‏ ‎‡9  1‏
919 ‎‡a  greenermediainchemicalsynthesisandprocessing‏ ‎‡A  Greener media in chemical synthesis and processing‏ ‎‡9  1‏
919 ‎‡a  rethinkingaromaticityinhbondedsystemscaveatsfortransitionstructuresinvolvinghydrogentransferandπdelocalization‏ ‎‡A  Rethinking aromaticity in H-bonded systems. Caveats for transition structures involving hydrogen transfer and π-delocalization‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
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996 ‎‡2  LC|nb2009006039‏
996 ‎‡2  DNB|1056421355‏
996 ‎‡2  BNE|XX1041182‏
996 ‎‡2  SUDOC|055836194‏
996 ‎‡2  NYNYRILM|150733‏
996 ‎‡2  DNB|171245776‏
996 ‎‡2  LC|no2019033474‏
996 ‎‡2  BNE|XX846122‏
996 ‎‡2  ISNI|0000000065411549‏
996 ‎‡2  BNE|XX1486902‏
996 ‎‡2  ISNI|0000000060340219‏
996 ‎‡2  SUDOC|130860719‏
996 ‎‡2  BNE|XX4605710‏
996 ‎‡2  SUDOC|154792756‏
996 ‎‡2  BNE|XX1058494‏
996 ‎‡2  SUDOC|114343691‏
996 ‎‡2  LC|ns2014005124‏
996 ‎‡2  BNE|XX5165918‏
996 ‎‡2  LC|no2014133865‏
996 ‎‡2  LC|nr 99005036‏
996 ‎‡2  BNF|16915100‏
996 ‎‡2  LC|n 2008076780‏
996 ‎‡2  ISNI|0000000033959091‏
996 ‎‡2  ISNI|0000000060246046‏
996 ‎‡2  BNE|XX868826‏
996 ‎‡2  BNE|XX1463811‏
996 ‎‡2  LC|n 88221559‏
996 ‎‡2  ISNI|000000008379423X‏
996 ‎‡2  SUDOC|085809853‏
996 ‎‡2  LC|no2011014195‏
996 ‎‡2  LC|ns2017002252‏
996 ‎‡2  BNE|XX6451685‏
996 ‎‡2  LC|no 95035097‏
996 ‎‡2  SZ|119359057‏
996 ‎‡2  BNE|XX1153978‏
996 ‎‡2  LC|ns2021003092‏
996 ‎‡2  BNE|XX1166087‏
996 ‎‡2  DNB|1056344679‏
996 ‎‡2  ISNI|0000000061004196‏
996 ‎‡2  ISNI|0000000078758349‏
996 ‎‡2  ISNI|0000000060617169‏
996 ‎‡2  BNE|XX1067638‏
996 ‎‡2  BNE|XX4831250‏
996 ‎‡2  LC|ns2022000264‏
996 ‎‡2  BNE|XX1524861‏
996 ‎‡2  RERO|A025279728‏
996 ‎‡2  ISNI|0000000119040369‏
996 ‎‡2  ISNI|0000000040003581‏
996 ‎‡2  LC|no2017100514‏
996 ‎‡2  CAOONL|ncf11241153‏
996 ‎‡2  BNC|981058511997506706‏
996 ‎‡2  BNE|XX1649910‏
996 ‎‡2  NTA|239253442‏
996 ‎‡2  ISNI|0000000034587381‏
996 ‎‡2  ISNI|0000000418483303‏
996 ‎‡2  LC|ns2013002697‏
996 ‎‡2  BNE|XX1121862‏
996 ‎‡2  BNC|981058608190106706‏
996 ‎‡2  BNE|XX1186575‏
996 ‎‡2  BNE|XX1288518‏
996 ‎‡2  BNE|XX1720522‏
996 ‎‡2  LC|n 2021023985‏
996 ‎‡2  LC|no2022028716‏
996 ‎‡2  DNB|171390822‏
996 ‎‡2  BNE|XX1019301‏
996 ‎‡2  BNE|XX1021318‏
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏