VIAF

Virtual International Authority File

Search

Leader 00000nz a2200037n 45 0
001 WKP|Q56980322 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241120235819.0
008 241120nneanz||abbn n and d
035 ‎‡a (WKP)Q56980322‏
024 ‎‡a 0000-0002-7261-8454‏ ‎‡2 orcid‏
024 ‎‡a 57202042078‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q56980322‏
100 0 ‎‡a David Díez‏ ‎‡c researcher‏ ‎‡9 en‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a David Díez‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's 1,3-Dipolar cycloaddition of nitrones with phenylvinyl sulfone. An experimental and theoretical study‏
670 ‎‡a Author's 1-Hydroxymethyl-4-phenylsulfonybutadiene, a versatile building block for the synthesis of 2,3,4-trisusbtituted tetrahydrothiophenes.‏
670 ‎‡a Author's (2R,3S,4R)-3,4-Isopropyl-idenedi-oxy-2-(phenyl-sulfonyl-meth-yl)pyrrolidin-1-ol.‏
670 ‎‡a Author's (3R,4S)-3,4-Isopropyl-idenedioxy-3,4-dihydro-2H-pyrrole 1-oxide.‏
670 ‎‡a Author's (3S*,4S*,E)-tert-Butyl 3,4-dibromo-5-oxo-cyclo-oct-1-ene-carboxyl-ate.‏
670 ‎‡a Author's A convenient asymmetric synthesis of a beta-amino ester with additional functionalization as a precursor for peptide nucleic acid‏
670 ‎‡a Author's A convenient asymmetric synthesis of a beta-amino ester with additional functionalization as a precursor for peptide nucleic acid (PNA) monomers‏
670 ‎‡a Author's A Novel Cytotoxic Conjugate Derived from the Natural Product Podophyllotoxin as a Direct-Target Protein Dual Inhibitor‏
670 ‎‡a Author's A novel strategy towards the asymmetric synthesis of orthogonally funtionalised 2-N-benzyl-N- Alpha -methylbenzylamino- 5-carboxymethyl-cyclopentane-1-carboxylic acid.‏
670 ‎‡a Author's Antibacterial and antioxidant activity of Portuguese Lavandula luisieri (Rozeira) Rivas-Martinez and its relation with their chemical composition‏
670 ‎‡a Author's Antibacterial Natural Halimanes: Potential Source of Novel Antibiofilm Agents‏
670 ‎‡a Author's Asymmetric synthesis of the stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate.‏
670 ‎‡a Author's Biomimetic synthesis of two salmahyrtisanes: salmahyrtisol A and hippospongide A.‏
670 ‎‡a Author's Chemistry of epoxysulfones: straightforward synthesis of versatile chiral building blocks‏
670 ‎‡a Author's Crystal structure of (2R*,3aR*)-2-phenyl-sulfonyl-2,3,3a,4,5,6-hexa-hydro-pyrrolo-[1,2-b]isoxazole.‏
670 ‎‡a Author's Crystal structure of methyl (4R)-4-(4-meth-oxy-benzo-yl)-4-{[(1R)-1-phenyl-eth-yl]carbamo-yl}butano-ate.‏
670 ‎‡a Author's Cyclic beta-amino acid derivatives: synthesis via lithium amide promoted tandem asymmetric conjugate addition-cyclisation reactions.‏
670 ‎‡a Author's Design, synthesis, pharmacological evaluation and molecular dynamics of β-amino acids morphan-derivatives as novel ligands for opioid receptors‏
670 ‎‡a Author's Diastereoselective synthesis of chiral 1,3-cyclohexadienals‏
670 ‎‡a Author's Diastereoselective synthesis of delta-aminoacids through domino Ireland-Claisen rearrangement and Michael addition‏
670 ‎‡a Author's Enantioselective synthesis of cis-decalins using organocatalysis and sulfonyl Nazarov reagents‏
670 ‎‡a Author's From labdanes to drimanes. Degradation of the side chain of dihydrozamoranic acid.‏
670 ‎‡a Author's Halimane diterpenoids: sources, structures, nomenclature and biological activities‏
670 ‎‡a Author's Hydrotalcite catalysis for the synthesis of new chiral building blocks‏
670 ‎‡a Author's Marine Alkylpurines: A Promising Group of Bioactive Marine Natural Products.‏
670 ‎‡a Author's Microbial hydroxylation of sclareol by Rhizopus stolonifer.‏
670 ‎‡a Author's Minor diterpenoids from Halimium viscosum‏
670 ‎‡a Author's Multicomponent Domino Reaction in the Asymmetric Synthesis of Cyclopentan[c]pyran Core of Iridoid Natural Products‏
670 ‎‡a Author's Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes.‏
670 ‎‡a Author's Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria‏
670 ‎‡a Author's Prenylflavonoids and prenyl/alkyl-phloroacetophenones: synthesis and antitumour biological evaluation.‏
670 ‎‡a Author's Preparation of methyl (1R,2S,5S)- and (1S,2R,5R)-2-amino-5-tert-butyl-cyclopentane-1-carboxylates by parallel kinetic resolution of methyl (RS)-5-tert-butyl-cyclopentene-1-carboxylate.‏
670 ‎‡a Author's Ring-closing metathesis as key step in the synthesis of Luffarin I, 16-epi-Luffarin I and Luffarin A.‏
670 ‎‡a Author's Sesquiterpenyl indoles‏
670 ‎‡a Author's Stereocontrolled synthesis of cyclopropanol amino acids from allylic sulfones: conformationally restricted building blocks‏
670 ‎‡a Author's Synergistic antibacterial activity of the essential oil of aguaribay‏
670 ‎‡a Author's Synergistic antibacterial activity of the essential oil of aguaribay (Schinus molle L.).‏
670 ‎‡a Author's Synthesis and bioactivity of Luffarin I.‏
670 ‎‡a Author's Synthesis and biological activity of polyalthenol and pentacyclindole analogues.‏
670 ‎‡a Author's Synthesis of a new chiral pyrrolidine‏
670 ‎‡a Author's Synthesis of an ent-halimanolide from ent-halimic acid‏
670 ‎‡a Author's Synthesis of Bioconjugate Sesterterpenoids with Phospholipids and Polyunsaturated Fatty Acids.‏
670 ‎‡a Author's Synthesis of Luffarin L and 16-epi-Luffarin L Using a Temporary Silicon-Tethered Ring-Closing Metathesis Reaction‏
670 ‎‡a Author's Synthesis of (R)-2-(benzyloxy)-tetrahydro-5,5-dimethylfuran by a new oxidative rearrangement‏
670 ‎‡a Author's Synthesis of three marine natural sesterterpenolides from methyl isoanticopalate. First enantioselective synthesis of luffolide‏
670 ‎‡a Author's Synthetic studies towards the ent-labdane diterpenoids: rearrangement of ent-halimanes‏
670 ‎‡a Author's The Methylene-Cycloalkylacetate (MCA) Scaffold in Terpenyl Compounds with Potential Pharmacological Activities‏
670 ‎‡a Author's To be or not to be butterfly: New mechanistic insights in the Aza-Michael asymmetric addition of lithium (R)-N-benzyl-N-(α-methylbenzyl)amide‏
670 ‎‡a Author's Yamaguchi-type lactonization as a key step in the synthesis of marine metabolites:‏
670 ‎‡a Author's Yamaguchi-type lactonization as a key step in the synthesis of marine metabolites: (+)-luffalactone.‏
909 ‎‡a (scopus) 57202042078‏ ‎‡9 1‏
909 ‎‡a (orcid) 0000000272618454‏ ‎‡9 1‏
919 ‎‡a yamaguchitypelactonizationasakeystepinthesynthesisofmarinemetabolites+luffalactone‏ ‎‡A Yamaguchi-type lactonization as a key step in the synthesis of marine metabolites: (+)-luffalactone.‏ ‎‡9 1‏
919 ‎‡a yamaguchitypelactonizationasakeystepinthesynthesisofmarinemetabolites‏ ‎‡A Yamaguchi-type lactonization as a key step in the synthesis of marine metabolites:‏ ‎‡9 1‏
919 ‎‡a tobeornottobebutterflynewmechanisticinsightsintheazamichaelasymmetricadditionoflithiumrnbenzylnαmethylbenzylamide‏ ‎‡A To be or not to be butterfly: New mechanistic insights in the Aza-Michael asymmetric addition of lithium (R)-N-benzyl-N-(α-methylbenzyl)amide‏ ‎‡9 1‏
919 ‎‡a methylenecycloalkylacetatemcascaffoldinterpenylcompoundswithpotenti Alpha rmacologicalactivities‏ ‎‡A The Methylene-Cycloalkylacetate (MCA) Scaffold in Terpenyl Compounds with Potential Pharmacological Activities‏ ‎‡9 1‏
919 ‎‡a syntheticstudiestowardstheentlabdanediterpenoidsrearrangementofenthalimanes‏ ‎‡A Synthetic studies towards the ent-labdane diterpenoids: rearrangement of ent-halimanes‏ ‎‡9 1‏
919 ‎‡a synthesisof3marinenaturalsesterterpenolidesfrommethylisoanticopalate1enantioselectivesynthesisofluffolide‏ ‎‡A Synthesis of three marine natural sesterterpenolides from methyl isoanticopalate. First enantioselective synthesis of luffolide‏ ‎‡9 1‏
919 ‎‡a synthesisofr2benzyloxytetrahydro55dimethylfuranbyanewoxidativerearrangement‏ ‎‡A Synthesis of (R)-2-(benzyloxy)-tetrahydro-5,5-dimethylfuran by a new oxidative rearrangement‏ ‎‡9 1‏
919 ‎‡a synthesisofluffarin50and16epiluffarin50usingatemporarysilicontetheredringclosingmetathesisreaction‏ ‎‡A Synthesis of Luffarin L and 16-epi-Luffarin L Using a Temporary Silicon-Tethered Ring-Closing Metathesis Reaction‏ ‎‡9 1‏
919 ‎‡a synthesisofbioconjugatesesterterpenoidswithphospholipidsandpolyunsaturatedfattyacids‏ ‎‡A Synthesis of Bioconjugate Sesterterpenoids with Phospholipids and Polyunsaturated Fatty Acids.‏ ‎‡9 1‏
919 ‎‡a synthesisofanenthalimanolidefromenthalimicacid‏ ‎‡A Synthesis of an ent-halimanolide from ent-halimic acid‏ ‎‡9 1‏
919 ‎‡a synthesisofanewchiralpyrrolidine‏ ‎‡A Synthesis of a new chiral pyrrolidine‏ ‎‡9 1‏
919 ‎‡a synthesisandbiologicalactivityofpolyalthenolandpentacyclindoleanalogues‏ ‎‡A Synthesis and biological activity of polyalthenol and pentacyclindole analogues.‏ ‎‡9 1‏
919 ‎‡a synthesisandbioactivityofluffarin1‏ ‎‡A Synthesis and bioactivity of Luffarin I.‏ ‎‡9 1‏
919 ‎‡a synergisticantibacterialactivityoftheessentialoilofaguaribayschinusmolle50‏ ‎‡A Synergistic antibacterial activity of the essential oil of aguaribay (Schinus molle L.).‏ ‎‡9 1‏
919 ‎‡a synergisticantibacterialactivityoftheessentialoilofaguaribay‏ ‎‡A Synergistic antibacterial activity of the essential oil of aguaribay‏ ‎‡9 1‏
919 ‎‡a stereocontrolledsynthesisofcyclopropanolaminoacidsfromallylicsulfonesconformationallyrestrictedbuildingblocks‏ ‎‡A Stereocontrolled synthesis of cyclopropanol amino acids from allylic sulfones: conformationally restricted building blocks‏ ‎‡9 1‏
919 ‎‡a sesquiterpenylindoles‏ ‎‡A Sesquiterpenyl indoles‏ ‎‡9 1‏
919 ‎‡a ringclosingmetathesisaskeystepinthesynthesisofluffarin116epiluffarin1andluffarina‏ ‎‡A Ring-closing metathesis as key step in the synthesis of Luffarin I, 16-epi-Luffarin I and Luffarin A.‏ ‎‡9 1‏
919 ‎‡a preparationofmethyl1r2s5sand1s2r5r2amino5tertbutylcyclopentane1carboxylatesbyparallelkineticresolutionofmethylrs5tertbutylcyclopentene1carboxylate‏ ‎‡A Preparation of methyl (1R,2S,5S)- and (1S,2R,5R)-2-amino-5-tert-butyl-cyclopentane-1-carboxylates by parallel kinetic resolution of methyl (RS)-5-tert-butyl-cyclopentene-1-carboxylate.‏ ‎‡9 1‏
919 ‎‡a prenylflavonoidsandprenylalkylphloroacetophenonessynthesisandantitumourbiologicalevaluation‏ ‎‡A Prenylflavonoids and prenyl/alkyl-phloroacetophenones: synthesis and antitumour biological evaluation.‏ ‎‡9 1‏
919 ‎‡a phytochemicalcompositionoflichenparmotremahypoleucinumjsteinerhalefromalgeria‏ ‎‡A Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria‏ ‎‡9 1‏
919 ‎‡a organocatalyzedsynthesisofbicyclooctanes‏ ‎‡A Organocatalyzed Synthesis of [3.2.1] Bicyclooctanes.‏ ‎‡9 1‏
919 ‎‡a multicomponentdominoreactionintheasymmetricsynthesisofcyclopentanpyrancoreofiridoidnaturalproducts‏ ‎‡A Multicomponent Domino Reaction in the Asymmetric Synthesis of Cyclopentan[c]pyran Core of Iridoid Natural Products‏ ‎‡9 1‏
919 ‎‡a minorditerpenoidsfromhalimiumviscosum‏ ‎‡A Minor diterpenoids from Halimium viscosum‏ ‎‡9 1‏
919 ‎‡a microbialhydroxylationofsclareolbyrhizopusstolonifer‏ ‎‡A Microbial hydroxylation of sclareol by Rhizopus stolonifer.‏ ‎‡9 1‏
919 ‎‡a marinealkylpurinesapromisinggroupofbioactivemarinenaturalproducts‏ ‎‡A Marine Alkylpurines: A Promising Group of Bioactive Marine Natural Products.‏ ‎‡9 1‏
919 ‎‡a hydrotalcitecatalysisforthesynthesisofnewchiralbuildingblocks‏ ‎‡A Hydrotalcite catalysis for the synthesis of new chiral building blocks‏ ‎‡9 1‏
919 ‎‡a halimanediterpenoidssourcesstructuresnomenclatureandbiologicalactivities‏ ‎‡A Halimane diterpenoids: sources, structures, nomenclature and biological activities‏ ‎‡9 1‏
919 ‎‡a fromlabdanestodrimanesdegradationofthesidechainofdihydrozamoranicacid‏ ‎‡A From labdanes to drimanes. Degradation of the side chain of dihydrozamoranic acid.‏ ‎‡9 1‏
919 ‎‡a enantioselectivesynthesisofcisdecalinsusingorganocatalysisandsulfonylnazarovreagents‏ ‎‡A Enantioselective synthesis of cis-decalins using organocatalysis and sulfonyl Nazarov reagents‏ ‎‡9 1‏
919 ‎‡a diastereoselectivesynthesisofdeltaaminoacidsthroughdominoirelandclaisenrearrangementandmichaeladdition‏ ‎‡A Diastereoselective synthesis of delta-aminoacids through domino Ireland-Claisen rearrangement and Michael addition‏ ‎‡9 1‏
919 ‎‡a diastereoselectivesynthesisofchiral13cyclohexadienals‏ ‎‡A Diastereoselective synthesis of chiral 1,3-cyclohexadienals‏ ‎‡9 1‏
919 ‎‡a designsynthesispharmacologicalevaluationandmoleculardynamicsofβaminoacidsmorphanderivativesasnovelligandsforopioidreceptors‏ ‎‡A Design, synthesis, pharmacological evaluation and molecular dynamics of β-amino acids morphan-derivatives as novel ligands for opioid receptors‏ ‎‡9 1‏
919 ‎‡a cyclicbetaaminoacidderivativessynthesisvialithiumamidepromotedtandemasymmetricconjugateadditioncyclisationreactions‏ ‎‡A Cyclic beta-amino acid derivatives: synthesis via lithium amide promoted tandem asymmetric conjugate addition-cyclisation reactions.‏ ‎‡9 1‏
919 ‎‡a crystalstructureofmethyl4r44methoxybenzoyl4carbamoylbutanoate‏ ‎‡A Crystal structure of methyl (4R)-4-(4-meth-oxy-benzo-yl)-4-{[(1R)-1-phenyl-eth-yl]carbamo-yl}butano-ate.‏ ‎‡9 1‏
919 ‎‡a crystalstructureof2r3ar2phenylsulfonyl233a456hexahydropyrroloisoxazole‏ ‎‡A Crystal structure of (2R*,3aR*)-2-phenyl-sulfonyl-2,3,3a,4,5,6-hexa-hydro-pyrrolo-[1,2-b]isoxazole.‏ ‎‡9 1‏
919 ‎‡a chemistryofepoxysulfonesstraightforwardsynthesisofversatilechiralbuildingblocks‏ ‎‡A Chemistry of epoxysulfones: straightforward synthesis of versatile chiral building blocks‏ ‎‡9 1‏
919 ‎‡a biomimeticsynthesisof2salmahyrtisanessalmahyrtisolaandhippospongidea‏ ‎‡A Biomimetic synthesis of two salmahyrtisanes: salmahyrtisol A and hippospongide A.‏ ‎‡9 1‏
919 ‎‡a asymmetricsynthesisofthestereoisomersof2amino5carboxymethylcyclopentane1carboxylate‏ ‎‡A Asymmetric synthesis of the stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate.‏ ‎‡9 1‏
919 ‎‡a antibacterialnaturalhalimanespotentialsourceofnovelantibiofilmagents‏ ‎‡A Antibacterial Natural Halimanes: Potential Source of Novel Antibiofilm Agents‏ ‎‡9 1‏
919 ‎‡a antibacterialandantioxidantactivityofportugueselavandulaluisierirozeirarivasmartinezanditsrelationwiththeirchemicalcomposition‏ ‎‡A Antibacterial and antioxidant activity of Portuguese Lavandula luisieri (Rozeira) Rivas-Martinez and its relation with their chemical composition‏ ‎‡9 1‏
919 ‎‡a novelstrategytowardstheasymmetricsynthesisoforthogonallyfuntionalised2nbenzyln Alpha methylbenzylamino5carboxymethylcyclopentane1carboxylicacid‏ ‎‡A A novel strategy towards the asymmetric synthesis of orthogonally funtionalised 2-N-benzyl-N- Alpha -methylbenzylamino- 5-carboxymethyl-cyclopentane-1-carboxylic acid.‏ ‎‡9 1‏
919 ‎‡a novelcytotoxicconjugatederivedfromthenaturalproductpodophyllotoxinasadirecttargetproteindualinhibitor‏ ‎‡A A Novel Cytotoxic Conjugate Derived from the Natural Product Podophyllotoxin as a Direct-Target Protein Dual Inhibitor‏ ‎‡9 1‏
919 ‎‡a convenientasymmetricsynthesisofabetaaminoesterwithadditionalfunctionalizationasaprecursorforpeptidenucleicacidpnamonomers‏ ‎‡A A convenient asymmetric synthesis of a beta-amino ester with additional functionalization as a precursor for peptide nucleic acid (PNA) monomers‏ ‎‡9 1‏
919 ‎‡a convenientasymmetricsynthesisofabetaaminoesterwithadditionalfunctionalizationasaprecursorforpeptidenucleicacid‏ ‎‡A A convenient asymmetric synthesis of a beta-amino ester with additional functionalization as a precursor for peptide nucleic acid‏ ‎‡9 1‏
919 ‎‡a 3s4setertbutyl34dibromo5oxocyclooct1enecarboxylate‏ ‎‡A (3S*,4S*,E)-tert-Butyl 3,4-dibromo-5-oxo-cyclo-oct-1-ene-carboxyl-ate.‏ ‎‡9 1‏
919 ‎‡a 3r4s34isopropylidenedioxy34dihydro2hpyrrole1oxide‏ ‎‡A (3R,4S)-3,4-Isopropyl-idenedioxy-3,4-dihydro-2H-pyrrole 1-oxide.‏ ‎‡9 1‏
919 ‎‡a 2r3s4r34isopropylidenedioxy2phenylsulfonylmethylpyrrolidin1ol‏ ‎‡A (2R,3S,4R)-3,4-Isopropyl-idenedi-oxy-2-(phenyl-sulfonyl-meth-yl)pyrrolidin-1-ol.‏ ‎‡9 1‏
919 ‎‡a 1hydroxymethyl4phenylsulfonybutadieneaversatilebuildingblockforthesynthesisof234trisusbtitutedtetrahydrothiophenes‏ ‎‡A 1-Hydroxymethyl-4-phenylsulfonybutadiene, a versatile building block for the synthesis of 2,3,4-trisusbtituted tetrahydrothiophenes.‏ ‎‡9 1‏
919 ‎‡a experimentalandtheoreticalstudy‏ ‎‡A An experimental and theoretical study‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
996 ‎‡2 NDL|031409615‏
996 ‎‡2 BNE|XX1031994‏
996 ‎‡2 BNE|XX4675273‏
996 ‎‡2 NUKAT|nx2022522456‏
996 ‎‡2 ISNI|0000000021194255‏
996 ‎‡2 PTBNP|1477360‏
996 ‎‡2 DNB|120179458‏
996 ‎‡2 DNB|120324539‏
996 ‎‡2 BNE|XX1130760‏
996 ‎‡2 ISNI|0000000059652805‏
996 ‎‡2 CAOONL|ncf13765901‏
996 ‎‡2 BNCHL|10000000000000000102816‏
996 ‎‡2 ISNI|0000000060603242‏
996 ‎‡2 BNE|XX5454322‏
996 ‎‡2 BNE|XX848542‏
996 ‎‡2 DNB|1234215772‏
996 ‎‡2 BNE|XX6232932‏
996 ‎‡2 BNF|18103202‏
996 ‎‡2 LC|n 2012038137‏
996 ‎‡2 ARBABN|000048631‏
996 ‎‡2 BNE|XX1617654‏
996 ‎‡2 BNE|XX1071888‏
996 ‎‡2 SUDOC|233232966‏
996 ‎‡2 ISNI|0000000361402479‏
996 ‎‡2 ISNI|000000006050886X‏
996 ‎‡2 ISNI|000000038193945X‏
996 ‎‡2 SUDOC|227282876‏
996 ‎‡2 J9U|987007420486705171‏
996 ‎‡2 ISNI|0000000068612346‏
996 ‎‡2 NKC|ntk20191043216‏
996 ‎‡2 BNE|XX1702089‏
996 ‎‡2 SUDOC|264612272‏
996 ‎‡2 ISNI|0000000512765307‏
996 ‎‡2 BNE|XX6321367‏
996 ‎‡2 ISNI|0000000061304439‏
996 ‎‡2 BNE|XX5377989‏
996 ‎‡2 SZ|1234215772‏
996 ‎‡2 PTBNP|365321‏
996 ‎‡2 LC|no2012043353‏
996 ‎‡2 BNC|981058517388406706‏
996 ‎‡2 DNB|171714644‏
996 ‎‡2 ISNI|0000000383461197‏
996 ‎‡2 BIBSYS|1560455410441‏
996 ‎‡2 DNB|1056534672‏
996 ‎‡2 LC|no2012122531‏
996 ‎‡2 BNC|981058525722306706‏
996 ‎‡2 LC|n 2001093145‏
996 ‎‡2 BNF|17978116‏
996 ‎‡2 SUDOC|158776321‏
996 ‎‡2 BNE|XX5149372‏
996 ‎‡2 W2Z|1560455410441‏
996 ‎‡2 BAV|495_113925‏
996 ‎‡2 BNE|XX868557‏
996 ‎‡2 BNC|981061159929506706‏
996 ‎‡2 DNB|128038373‏
996 ‎‡2 LC|ns2017000421‏
996 ‎‡2 BNE|XX5728425‏
996 ‎‡2 ISNI|0000000428274310‏
996 ‎‡2 NUKAT|n 2018143612‏
996 ‎‡2 NII|DA19112484‏
996 ‎‡2 DNB|142767344‏
996 ‎‡2 BNE|XX1162538‏
996 ‎‡2 DNB|1071011650‏
996 ‎‡2 LC|no2024101418‏
996 ‎‡2 DNB|172799368‏
996 ‎‡2 BNE|XX6443006‏
996 ‎‡2 RERO|A020413352‏
996 ‎‡2 DNB|129745782‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏