VIAF

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Leader     00000nz a2200037n 45 0
001     WKP|Q77647101  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241221010739.0
008     241221nneanz||abbn n and d
035 ‎‡a  (WKP)Q77647101‏
024 ‎‡a  0000-0001-7394-2101‏ ‎‡2  orcid‏
024 ‎‡a  36469764300‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q77647101‏
100 0 ‎‡a  Jason E Camp‏ ‎‡c  researcher‏ ‎‡9  en‏
400 0 ‎‡a  Jason E Camp‏ ‎‡c  wetenschapper‏ ‎‡9  nl‏
670 ‎‡a  Author's Bio-available Solvent Cyrene: Synthesis, Derivatization, and Applications‏
670 ‎‡a  Author's Charge-transfer dynamics at the dye-semiconductor interface of photocathodes for solar energy applications‏
670 ‎‡a  Author's Construction of beta-haloenamides via direct copper-promoted coupling of lactams with 2-chloro and 2-bromo vinyliodides.‏
670 ‎‡a  Author's Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines‏
670 ‎‡a  Author's Development of a gold-multifaceted catalysis approach to the synthesis of highly substituted pyrroles: mechanistic insights via Huisgen cycloaddition studies.‏
670 ‎‡a  Author's Exploring the Reactivity of 2-Trichloromethylbenzoxazoles for Access to Substituted Benzoxazoles.‏
670 ‎‡a  Author's Gold-catalysed rearrangement of O-vinyl oximes for the synthesis of highly substituted pyrroles‏
670 ‎‡a  Author's meso Substituent effects on the geometric and electronic structures of high-spin and low-spin iron‏
670 ‎‡a  Author's meso Substituent effects on the geometric and electronic structures of high-spin and low-spin iron(III) complexes of mono-meso-substituted octaethylporphyrins.‏
670 ‎‡a  Author's Multifaceted catalysis approach to nitrile activation: direct synthesis of halogenated allyl amides from allylic alcohols‏
670 ‎‡a  Author's Recent advances in the synthesis of imidazoles‏
670 ‎‡a  Author's Resonance Raman Study of New Pyrrole-Anchoring Dyes for NiO-Sensitized Solar Cells.‏
909 ‎‡a  (orcid) 0000000173942101‏ ‎‡9  1‏
909 ‎‡a  (scopus) 36469764300‏ ‎‡9  1‏
919 ‎‡a  resonanceramanstudyofnewpyrroleanchoringdyesforniosensitizedsolarcells‏ ‎‡A  Resonance Raman Study of New Pyrrole-Anchoring Dyes for NiO-Sensitized Solar Cells.‏ ‎‡9  1‏
919 ‎‡a  recentadvancesinthesynthesisofimidazoles‏ ‎‡A  Recent advances in the synthesis of imidazoles‏ ‎‡9  1‏
919 ‎‡a  multifacetedcatalysisapproachtonitrileactivationdirectsynthesisofhalogenatedallylamidesfromallylicalcohols‏ ‎‡A  Multifaceted catalysis approach to nitrile activation: direct synthesis of halogenated allyl amides from allylic alcohols‏ ‎‡9  1‏
919 ‎‡a  mesosubstituenteffectsonthegeometricandelectronicstructuresofhighspinandlowspiniron3complexesofmonomesosubstitutedoctaethylporphyrins‏ ‎‡A  meso Substituent effects on the geometric and electronic structures of high-spin and low-spin iron(III) complexes of mono-meso-substituted octaethylporphyrins.‏ ‎‡9  1‏
919 ‎‡a  mesosubstituenteffectsonthegeometricandelectronicstructuresofhighspinandlowspiniron‏ ‎‡A  meso Substituent effects on the geometric and electronic structures of high-spin and low-spin iron‏ ‎‡9  1‏
919 ‎‡a  bioavailablesolventcyrenesynthesisderivatizationandapplications‏ ‎‡A  Bio-available Solvent Cyrene: Synthesis, Derivatization, and Applications‏ ‎‡9  1‏
919 ‎‡a  chargetransferdynamicsatthedyesemiconductorinterfaceofphotocathodesforsolarenergyapplications‏ ‎‡A  Charge-transfer dynamics at the dye-semiconductor interface of photocathodes for solar energy applications‏ ‎‡9  1‏
919 ‎‡a  constructionofbetahaloenamidesviadirectcopperpromotedcouplingoflactamswith2chloroand2bromovinyliodides‏ ‎‡A  Construction of beta-haloenamides via direct copper-promoted coupling of lactams with 2-chloro and 2-bromo vinyliodides.‏ ‎‡9  1‏
919 ‎‡a  decarboxylativeclaisenrearrangementreactionssynthesisandreactivityofalkylidenesubstitutedindolines‏ ‎‡A  Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines‏ ‎‡9  1‏
919 ‎‡a  developmentofagoldmultifacetedcatalysisapproachtothesynthesisofhighlysubstitutedpyrrolesmechanisticinsightsviahuisgencycloadditionstudies‏ ‎‡A  Development of a gold-multifaceted catalysis approach to the synthesis of highly substituted pyrroles: mechanistic insights via Huisgen cycloaddition studies.‏ ‎‡9  1‏
919 ‎‡a  exploringthereactivityof2trichloromethylbenzoxazolesforaccesstosubstitutedbenzoxazoles‏ ‎‡A  Exploring the Reactivity of 2-Trichloromethylbenzoxazoles for Access to Substituted Benzoxazoles.‏ ‎‡9  1‏
919 ‎‡a  goldcatalysedrearrangementofovinyloximesforthesynthesisofhighlysubstitutedpyrroles‏ ‎‡A  Gold-catalysed rearrangement of O-vinyl oximes for the synthesis of highly substituted pyrroles‏ ‎‡9  1‏
996 ‎‡2  PLWABN|9812424802805606
996 ‎‡2  LC|no2018084021
996 ‎‡2  LC|no2020123173
996 ‎‡2  RERO|A003072122
996 ‎‡2  NUKAT|n 2021089265
996 ‎‡2  LC|n 81021741
996 ‎‡2  JPG|500061693
996 ‎‡2  BIBSYS|4006737
996 ‎‡2  ISNI|0000000392358984
996 ‎‡2  NTA|068779313
996 ‎‡2  BNF|16578595
996 ‎‡2  DNB|134342623
996 ‎‡2  ISNI|0000000035858016
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏