VIAF

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Leader 00000nz a2200037n 45 0
001 WKP|Q56536394 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000330.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q56536394‏
024 ‎‡a 0000-0001-8314-1877‏ ‎‡2 orcid‏
024 ‎‡a 7004747434‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q56536394‏
043 ‎‡c GB‏
100 0 ‎‡a Philip Charles Bulman Page‏ ‎‡c British organic chemist‏ ‎‡9 en‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a Philip Charles Bulman Page‏ ‎‡c scheikundige‏ ‎‡9 nl‏
400 0 ‎‡a Philip Charles Bulman Page‏ ‎‡c investigador‏ ‎‡9 es‏
670 ‎‡a Author's A gold-gold oil microtrench electrode for liquid-liquid anion transfer voltammetry.‏
670 ‎‡a Author's A new twist in the photophysics of the GFP chromophore: a volume-conserving molecular torsion couple.‏
670 ‎‡a Author's Asymmetric Oxidation of Enol Derivatives to α-Alkoxy Carbonyls Using Iminium Salt Catalysts: A Synthetic and Computational Study‏
670 ‎‡a Author's Atropo- and Diastereoselective Construction of Tetracyclic Biphenylazepinium Salts Derived from Aminoalcohols: Use as Catalysts in Enantioselective Asymmetric Epoxidation‏
670 ‎‡a Author's Dimethylsulfoniopropionate biosynthesis in marine bacteria and identification of the key gene in this process‏
670 ‎‡a Author's Discovery of Small Molecule WWP2 Ubiquitin Ligase Inhibitors‏
670 ‎‡a Author's Formal Total Synthesis of‏
670 ‎‡a Author's Formal Total Synthesis of (+)-C9-Deoxyomuralide from l-Leucine Using a Double Sacrificial Chirality Transfer Approach.‏
670 ‎‡a Author's Front Cover: Induction of Planar Chirality Using Asymmetric Click Chemistry by a Novel Desymmetrisation of 1,3-Bisalkynyl Ferrocenes (Eur. J. Org. Chem. 43/2019)‏
670 ‎‡a Author's Iminium salt catalysts for asymmetric epoxidation: the first high enantioselectivities‏
670 ‎‡a Author's Induction of Planar Chirality Using Asymmetric Click Chemistry by a Novel Desymmetrisation of 1,3-Bisalkynyl Ferrocenes‏
670 ‎‡a Author's "Janus" Calixarenes: Double-Sided Molecular Linkers for Facile, Multianchor Point, Multifunctional, Surface Modification‏
670 ‎‡a Author's Liquid-liquid ion transport junctions based on paired gold electrodes in generator-collector mode‏
670 ‎‡a Author's New biphenyl iminium salt catalysts for highly enantioselective asymmetric epoxidation: role of additional substitution and dihedral angle.‏
670 ‎‡a Author's Novel binaphthyl and biphenyl α- and β-amino acids and esters: organocatalysis of asymmetric Diels-Alder reactions. A combined synthetic and computational study‏
670 ‎‡a Author's One- to Two-Exciton Transitions in Perylene Bisimide Dimer Revealed by Two-Dimensional Electronic Spectroscopy‏
670 ‎‡a Author's Short and versatile route to a key intermediate for lactacystin synthesis‏
670 ‎‡a Author's Synthesis and Activity of a Novel Autotaxin Inhibitor-Icodextrin Conjugate‏
670 ‎‡a Author's The Effect of Conjugation on the Competition between Internal Conversion and Electron Detachment: A Comparison between Green Fluorescent and Red Kaede Protein Chromophores.‏
670 ‎‡a Author's Ultrafast Studies of the Photophysics of Cis and Trans States of the Green Fluorescent Protein Chromophore‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/NUKAT|n 99036604‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/ISNI|0000000083982513‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/NTA|186446950‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/BIBSYS|99067382‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/viaf/85121346‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/LC|no 00000422‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/SUDOC|166612138‏
909 ‎‡a (scopus) 7004747434‏ ‎‡9 1‏
909 ‎‡a (orcid) 0000000183141877‏ ‎‡9 1‏
919 ‎‡a asymmetricoxidationofenolderivativestoαalkoxycarbonylsusingiminiumsaltcatalystsasyntheticandcomputationalstudy‏ ‎‡A Asymmetric Oxidation of Enol Derivatives to α-Alkoxy Carbonyls Using Iminium Salt Catalysts: A Synthetic and Computational Study‏ ‎‡9 1‏
919 ‎‡a dimethylsulfoniopropionatebiosynthesisinmarinebacteriaandidentificationofthekeygeneinthisprocess‏ ‎‡A Dimethylsulfoniopropionate biosynthesis in marine bacteria and identification of the key gene in this process‏ ‎‡9 1‏
919 ‎‡a discoveryofsmallmoleculewwp2ubiquitinligaseinhibitors‏ ‎‡A Discovery of Small Molecule WWP2 Ubiquitin Ligase Inhibitors‏ ‎‡9 1‏
919 ‎‡a formaltotalsynthesisof‏ ‎‡A Formal Total Synthesis of‏ ‎‡9 1‏
919 ‎‡a formaltotalsynthesisof+c9deoxyomuralidefrom50leucineusingadoublesacrificialchiralitytransferapproach‏ ‎‡A Formal Total Synthesis of (+)-C9-Deoxyomuralide from l-Leucine Using a Double Sacrificial Chirality Transfer Approach.‏ ‎‡9 1‏
919 ‎‡a frontcoverinductionofplanarchiralityusingasymmetricclickchemistrybyanoveldesymmetrisationof13bisalkynylferroceneseurjorgchem43‏ ‎‡A Front Cover: Induction of Planar Chirality Using Asymmetric Click Chemistry by a Novel Desymmetrisation of 1,3-Bisalkynyl Ferrocenes (Eur. J. Org. Chem. 43/2019)‏ ‎‡9 1‏
919 ‎‡a iminiumsaltcatalystsforasymmetricepoxidationthe1highenantioselectivities‏ ‎‡A Iminium salt catalysts for asymmetric epoxidation: the first high enantioselectivities‏ ‎‡9 1‏
919 ‎‡a inductionofplanarchiralityusingasymmetricclickchemistrybyanoveldesymmetrisationof13bisalkynylferrocenes‏ ‎‡A Induction of Planar Chirality Using Asymmetric Click Chemistry by a Novel Desymmetrisation of 1,3-Bisalkynyl Ferrocenes‏ ‎‡9 1‏
919 ‎‡a januscalixarenesdoublesidedmolecularlinkersforfacilemultianchorpointmultifunctionalsurfacemodification‏ ‎‡A "Janus" Calixarenes: Double-Sided Molecular Linkers for Facile, Multianchor Point, Multifunctional, Surface Modification‏ ‎‡9 1‏
919 ‎‡a liquidliquidiontransportjunctionsbasedonpairedgoldelectrodesingeneratorcollectormode‏ ‎‡A Liquid-liquid ion transport junctions based on paired gold electrodes in generator-collector mode‏ ‎‡9 1‏
919 ‎‡a newbiphenyliminiumsaltcatalystsforhighlyenantioselectiveasymmetricepoxidationroleofadditionalsubstitutionanddihedralangle‏ ‎‡A New biphenyl iminium salt catalysts for highly enantioselective asymmetric epoxidation: role of additional substitution and dihedral angle.‏ ‎‡9 1‏
919 ‎‡a novelbinaphthylandbiphenylαandβaminoacidsandestersorganocatalysisofasymmetricdielsalderreactionsacombinedsyntheticandcomputationalstudy‏ ‎‡A Novel binaphthyl and biphenyl α- and β-amino acids and esters: organocatalysis of asymmetric Diels-Alder reactions. A combined synthetic and computational study‏ ‎‡9 1‏
919 ‎‡a 1to2excitontransitionsinperylenebisimidedimerrevealedby2dimensionalelectronicspectroscopy‏ ‎‡A One- to Two-Exciton Transitions in Perylene Bisimide Dimer Revealed by Two-Dimensional Electronic Spectroscopy‏ ‎‡9 1‏
919 ‎‡a shortandversatileroutetoakeyintermediateforlactacystinsynthesis‏ ‎‡A Short and versatile route to a key intermediate for lactacystin synthesis‏ ‎‡9 1‏
919 ‎‡a synthesisandactivityofanovelautotaxininhibitoricodextrinconjugate‏ ‎‡A Synthesis and Activity of a Novel Autotaxin Inhibitor-Icodextrin Conjugate‏ ‎‡9 1‏
919 ‎‡a effectofconjugationonthecompetitionbetweeninternalconversionandelectrondetachmentacomparisonbetweengreenfluorescentandredkaedeproteinchromophores‏ ‎‡A The Effect of Conjugation on the Competition between Internal Conversion and Electron Detachment: A Comparison between Green Fluorescent and Red Kaede Protein Chromophores.‏ ‎‡9 1‏
919 ‎‡a ultrafaststudiesofthephotophysicsofcisandtransstatesofthegreenfluorescentproteinchromophore‏ ‎‡A Ultrafast Studies of the Photophysics of Cis and Trans States of the Green Fluorescent Protein Chromophore‏ ‎‡9 1‏
919 ‎‡a atropoanddiastereoselectiveconstructionoftetracyclicbiphenylazepiniumsaltsderivedfromaminoalcoholsuseascatalystsinenantioselectiveasymmetricepoxidation‏ ‎‡A Atropo- and Diastereoselective Construction of Tetracyclic Biphenylazepinium Salts Derived from Aminoalcohols: Use as Catalysts in Enantioselective Asymmetric Epoxidation‏ ‎‡9 1‏
919 ‎‡a goldgoldoilmicrotrenchelectrodeforliquidliquidaniontransfervoltammetry‏ ‎‡A A gold-gold oil microtrench electrode for liquid-liquid anion transfer voltammetry.‏ ‎‡9 1‏
919 ‎‡a newtwistinthephotophysicsofthegfpchromophoreavolumeconservingmoleculartorsioncouple‏ ‎‡A A new twist in the photophysics of the GFP chromophore: a volume-conserving molecular torsion couple.‏ ‎‡9 1‏
943 ‎‡a 201x‏ ‎‡A 2019‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
947 ‎‡a GB‏ ‎‡9 1‏
996 ‎‡2 CAOONL|ncf11276580‏
996 ‎‡2 J9U|987012748030405171‏
996 ‎‡2 BIBSYS|40378‏
996 ‎‡2 SUDOC|240277708‏
996 ‎‡2 SUDOC|160475473‏
996 ‎‡2 CAOONL|ncf11231104‏
996 ‎‡2 ISNI|0000000075792955‏
996 ‎‡2 J9U|987007458513105171‏
996 ‎‡2 NUKAT|n 01195776‏
996 ‎‡2 N6I|vtls000112420‏
996 ‎‡2 NKC|pna2007397613‏
996 ‎‡2 LC|n 80162034‏
996 ‎‡2 NII|DA07935434‏
996 ‎‡2 DNB|1229387595‏
996 ‎‡2 LC|no 00000422‏
996 ‎‡2 BNF|11810617‏
996 ‎‡2 SUDOC|166612138‏
996 ‎‡2 ISNI|0000000114617982‏
996 ‎‡2 NUKAT|n 2020021212‏
996 ‎‡2 ISNI|0000000384606298‏
996 ‎‡2 LC|n 2002133695‏
996 ‎‡2 NUKAT|n 99036604‏
996 ‎‡2 BNF|14553036‏
996 ‎‡2 SUDOC|107978296‏
996 ‎‡2 NKC|mub2010605934‏
996 ‎‡2 NUKAT|n 01011193‏
996 ‎‡2 BIBSYS|4024124‏
996 ‎‡2 CAOONL|ncf10904994‏
996 ‎‡2 LC|no2006020264‏
996 ‎‡2 ISNI|0000000082651851‏
996 ‎‡2 NTA|186446950‏
996 ‎‡2 BNF|12307839‏
996 ‎‡2 ISNI|0000000027244719‏
996 ‎‡2 ISNI|0000000083982513‏
996 ‎‡2 ISNI|0000000388648217‏
996 ‎‡2 BIBSYS|90826771‏
996 ‎‡2 PLWABN|9810571970905606‏
996 ‎‡2 ISNI|0000000117357389‏
996 ‎‡2 BNF|12502128‏
996 ‎‡2 NSK|000241301‏
996 ‎‡2 ISNI|0000000459569314‏
996 ‎‡2 J9U|987007396389205171‏
996 ‎‡2 BNF|14616343‏
996 ‎‡2 KRNLK|KAC200505167‏
996 ‎‡2 RERO|A020093352‏
996 ‎‡2 BIBSYS|11080523‏
996 ‎‡2 CAOONL|ncf12109315‏
996 ‎‡2 J9U|987012798309805171‏
996 ‎‡2 SUDOC|279962517‏
996 ‎‡2 SUDOC|156235005‏
996 ‎‡2 ISNI|0000000081258521‏
996 ‎‡2 SUDOC|268969108‏
996 ‎‡2 LC|no2001061376‏
996 ‎‡2 ISNI|0000000048500208‏
996 ‎‡2 B2Q|0000126641‏
996 ‎‡2 LC|nb2015022107‏
996 ‎‡2 SUDOC|034246053‏
996 ‎‡2 NUKAT|n 2018295688‏
996 ‎‡2 LC|n 95096225‏
996 ‎‡2 CAOONL|ncf11849677‏
996 ‎‡2 LC|nb2014010870‏
996 ‎‡2 NII|DA10029960‏
996 ‎‡2 J9U|987007335807905171‏
996 ‎‡2 BNF|17032938‏
996 ‎‡2 ISNI|0000000021905926‏
996 ‎‡2 SUDOC|031957862‏
996 ‎‡2 NTA|121159175‏
996 ‎‡2 RERO|A003664836‏
996 ‎‡2 LC|no2009083533‏
996 ‎‡2 LC|no2016029187‏
996 ‎‡2 ISNI|0000000451428648‏
996 ‎‡2 BIBSYS|90621037‏
996 ‎‡2 NTA|312652453‏
996 ‎‡2 NDL|01029672‏
996 ‎‡2 DNB|1141325977‏
996 ‎‡2 SUDOC|153006110‏
996 ‎‡2 RERO|A003664901‏
996 ‎‡2 ISNI|0000000384753749‏
996 ‎‡2 RERO|A000048283‏
996 ‎‡2 RERO|A003664902‏
996 ‎‡2 NUKAT|n 2012179594‏
996 ‎‡2 LC|nr 00027361‏
996 ‎‡2 CAOONL|ncf11020616‏
996 ‎‡2 NTA|326741224‏
996 ‎‡2 BIBSYS|8050514‏
996 ‎‡2 DBC|87097991777207‏
996 ‎‡2 LC|n 88667348‏
996 ‎‡2 NUKAT|n 2007153641‏
996 ‎‡2 NUKAT|n 2017236772‏
996 ‎‡2 BNF|13482728‏
996 ‎‡2 J9U|987007429234005171‏
996 ‎‡2 BIBSYS|99067382‏
996 ‎‡2 ISNI|0000000083604176‏
996 ‎‡2 DNB|1146454074‏
996 ‎‡2 LNB|LNC10-000098413‏
996 ‎‡2 SUDOC|090961633‏
996 ‎‡2 J9U|987007460904505171‏
996 ‎‡2 LC|nr2004014251‏
996 ‎‡2 LC|n 83214307‏
996 ‎‡2 NTA|072350482‏
996 ‎‡2 CAOONL|ncf10089080‏
996 ‎‡2 LC|n 88114546‏
996 ‎‡2 SUDOC|118586556‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏
998 ‎‡a Page, Philip C.B.‏ ‎‡2 SUDOC|166612138‏ ‎‡3 suggested‏
998 ‎‡a Page, Philip C.B.‏ ‎‡2 BIBSYS|99067382‏ ‎‡3 suggested‏ ‎‡3 viafid‏
998 ‎‡a Page, Philip C.B.‏ ‎‡2 NTA|186446950‏ ‎‡3 suggested‏
998 ‎‡a Page, Philip C. B.‏ ‎‡2 J9U|987007460904505171‏ ‎‡3 suggested‏
998 ‎‡a Page, Philip C. B.‏ ‎‡2 LC|no 00000422‏ ‎‡3 suggested‏
998 ‎‡a Page, Philip C.B.‏ ‎‡2 ISNI|0000000083982513‏ ‎‡3 suggested‏
998 ‎‡a Page, Philip C.B.‏ ‎‡2 ISNI|0000000083982513‏ ‎‡3 suggested‏
998 ‎‡a Page, Philip C. B.‏ ‎‡2 ISNI|0000000083982513‏ ‎‡3 suggested‏
998 ‎‡a Page, Philip C. B.‏ ‎‡2 NUKAT|n 99036604‏ ‎‡3 suggested‏ ‎‡3 viafid‏