VIAF

Virtual International Authority File

Search

Leader     00000nz a2200037n 45 0
001     WKP|Q87826805  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241221010900.0
008     241221nneanz||abbn n and d
035 ‎‡a  (WKP)Q87826805‏
024 ‎‡a  0000-0002-5538-1555‏ ‎‡2  orcid‏
035 ‎‡a  (OCoLC)Q87826805‏
100 0 ‎‡a  Daniel G Rivera‏ ‎‡c  researcher‏ ‎‡9  en‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  Daniel G Rivera‏ ‎‡c  onderzoeker‏ ‎‡9  nl‏
670 ‎‡a  Author's A multicomponent macrocyclization strategy to natural product-like cyclic lipopeptides: synthesis and anticancer evaluation of surfactin and mycosubtilin analogues.‏
670 ‎‡a  Author's A Multicomponent Stapling Approach to Exocyclic Functionalized Helical Peptides: Adding Lipids, Sugars, PEGs, Labels, and Handles to the Lactam Bridge‏
670 ‎‡a  Author's A Peptide Backbone Stapling Strategy Enabled by the Multicomponent Incorporation of Amide N-Substituents‏
670 ‎‡a  Author's A stereoselective sequential organocascade and multicomponent approach for the preparation of tetrahydropyridines and chimeric derivatives‏
670 ‎‡a  Author's Action Items for Latin-American Chemists and Chemical Societies to Improve Equity and Diversity in Science‏
670 ‎‡a  Author's Combining the Ugi-azide multicomponent reaction and rhodium(III)-catalyzed annulation for the synthesis of tetrazole-isoquinolone/pyridone hybrids‏
670 ‎‡a  Author's CuICuII and AgIp-isocyanobenzoates as novel 1D semiconducting coordination oligomers‏
670 ‎‡a  Author's Design of a Helical-Stabilized, Cyclic, and Nontoxic Analogue of the Peptide Cm-p5 with Improved Antifungal Activity‏
670 ‎‡a  Author's Diversity Driven Decoration and Ligation of Fullerene by Ugi and Passerini Multicomponent Reactions‏
670 ‎‡a  Author's Improved Stability and Tunable Functionalization of Parallel β-Sheets via Multicomponent N-Alkylation of the Turn Moiety‏
670 ‎‡a  Author's Insights into the secondary structures of lactam N-substituted stapled peptides‏
670 ‎‡a  Author's Introducing the Petasis Reaction for Late-Stage Multicomponent Diversification, Labeling, and Stapling of Peptides‏
670 ‎‡a  Author's Multi-Institution Research and Education Collaboration Identifies New Antimicrobial Compounds‏
670 ‎‡a  Author's Multicomponent polysaccharide-protein bioconjugation in the development of antibacterial glycoconjugate vaccine candidates.‏
670 ‎‡a  Author's Multicomponent Reaction Toolbox for Peptide Macrocyclization and Stapling‏
670 ‎‡a  Author's Multicomponent Reactions in Ligation and Bioconjugation Chemistry‏
670 ‎‡a  Author's Peptide Macrocyclization Assisted by Traceless Turn Inducers Derived from Ugi Peptide Ligation with Cleavable and Resin-Linked Amines.‏
670 ‎‡a  Author's Peptide macrocyclization by transition metal catalysis‏
670 ‎‡a  Author's Stabilization of Cyclic β-Hairpins by Ugi-Reaction-Derived N-Alkylated Peptides: The Quest for Functionalized β-Turns‏
670 ‎‡a  Author's Steroid diversification by multicomponent reactions‏
670 ‎‡a  Author's Ugi reaction-derived prolyl peptide catalysts grafted on the renewable polymer polyfurfuryl alcohol for applications in heterogeneous enamine catalysis‏
909 ‎‡a  (orcid) 0000000255381555‏ ‎‡9  1‏
919 ‎‡a  multicomponentreactionsinligationandbioconjugationchemistry‏ ‎‡A  Multicomponent Reactions in Ligation and Bioconjugation Chemistry‏ ‎‡9  1‏
919 ‎‡a  peptidemacrocyclizationassistedbytracelessturninducersderivedfromugipeptideligationwithcleavableandresinlinkedamines‏ ‎‡A  Peptide Macrocyclization Assisted by Traceless Turn Inducers Derived from Ugi Peptide Ligation with Cleavable and Resin-Linked Amines.‏ ‎‡9  1‏
919 ‎‡a  peptidemacrocyclizationbytransitionmetalcatalysis‏ ‎‡A  Peptide macrocyclization by transition metal catalysis‏ ‎‡9  1‏
919 ‎‡a  stabilizationofcyclicβhairpinsbyugireactionderivednalkylatedpeptidesthequestforfunctionalizedβturns‏ ‎‡A  Stabilization of Cyclic β-Hairpins by Ugi-Reaction-Derived N-Alkylated Peptides: The Quest for Functionalized β-Turns‏ ‎‡9  1‏
919 ‎‡a  steroiddiversificationbymulticomponentreactions‏ ‎‡A  Steroid diversification by multicomponent reactions‏ ‎‡9  1‏
919 ‎‡a  multicomponentmacrocyclizationstrategytonaturalproductlikecycliclipopeptidessynthesisandanticancerevaluationofsurfactinandmycosubtilinanalogues‏ ‎‡A  A multicomponent macrocyclization strategy to natural product-like cyclic lipopeptides: synthesis and anticancer evaluation of surfactin and mycosubtilin analogues.‏ ‎‡9  1‏
919 ‎‡a  multicomponentstaplingapproachtoexocyclicfunctionalizedhelicalpeptidesaddinglipidssugarspegslabelsandhandlestothelactambridge‏ ‎‡A  A Multicomponent Stapling Approach to Exocyclic Functionalized Helical Peptides: Adding Lipids, Sugars, PEGs, Labels, and Handles to the Lactam Bridge‏ ‎‡9  1‏
919 ‎‡a  peptidebackbonestaplingstrategyenabledbythemulticomponentincorporationofamidensubstituents‏ ‎‡A  A Peptide Backbone Stapling Strategy Enabled by the Multicomponent Incorporation of Amide N-Substituents‏ ‎‡9  1‏
919 ‎‡a  stereoselectivesequentialorganocascadeandmulticomponentapproachforthepreparationoftetrahydropyridinesandchimericderivatives‏ ‎‡A  A stereoselective sequential organocascade and multicomponent approach for the preparation of tetrahydropyridines and chimeric derivatives‏ ‎‡9  1‏
919 ‎‡a  actionitemsforlatinamericanchemistsandchemicalsocietiestoimproveequityanddiversityinscience‏ ‎‡A  Action Items for Latin-American Chemists and Chemical Societies to Improve Equity and Diversity in Science‏ ‎‡9  1‏
919 ‎‡a  combiningtheugiazidemulticomponentreactionandrhodium3catalyzedannulationforthesynthesisoftetrazoleisoquinolonepyridonehybrids‏ ‎‡A  Combining the Ugi-azide multicomponent reaction and rhodium(III)-catalyzed annulation for the synthesis of tetrazole-isoquinolone/pyridone hybrids‏ ‎‡9  1‏
919 ‎‡a  cuicuiiandagipisocyanobenzoatesasnovel1dsemiconductingcoordinationoligomers‏ ‎‡A  CuICuII and AgIp-isocyanobenzoates as novel 1D semiconducting coordination oligomers‏ ‎‡9  1‏
919 ‎‡a  designofahelicalstabilizedcyclicandnontoxicanalogueofthepeptide900p5withimprovedantifungalactivity‏ ‎‡A  Design of a Helical-Stabilized, Cyclic, and Nontoxic Analogue of the Peptide Cm-p5 with Improved Antifungal Activity‏ ‎‡9  1‏
919 ‎‡a  diversitydrivendecorationandligationoffullerenebyugiandpasserinimulticomponentreactions‏ ‎‡A  Diversity Driven Decoration and Ligation of Fullerene by Ugi and Passerini Multicomponent Reactions‏ ‎‡9  1‏
919 ‎‡a  ugireactionderivedprolylpeptidecatalystsgraftedontherenewablepolymerpolyfurfurylalcoholforapplicationsinheterogeneousenaminecatalysis‏ ‎‡A  Ugi reaction-derived prolyl peptide catalysts grafted on the renewable polymer polyfurfuryl alcohol for applications in heterogeneous enamine catalysis‏ ‎‡9  1‏
919 ‎‡a  improvedstabilityandtunablefunctionalizationofparallelβsheetsviamulticomponentnalkylationoftheturnmoiety‏ ‎‡A  Improved Stability and Tunable Functionalization of Parallel β-Sheets via Multicomponent N-Alkylation of the Turn Moiety‏ ‎‡9  1‏
919 ‎‡a  insightsintothesecondarystructuresoflactamnsubstitutedstapledpeptides‏ ‎‡A  Insights into the secondary structures of lactam N-substituted stapled peptides‏ ‎‡9  1‏
919 ‎‡a  introducingthepetasisreactionforlatestagemulticomponentdiversificationlabelingandstaplingofpeptides‏ ‎‡A  Introducing the Petasis Reaction for Late-Stage Multicomponent Diversification, Labeling, and Stapling of Peptides‏ ‎‡9  1‏
919 ‎‡a  multiinstitutionresearchandeducationcollaborationidentifiesnewantimicrobialcompounds‏ ‎‡A  Multi-Institution Research and Education Collaboration Identifies New Antimicrobial Compounds‏ ‎‡9  1‏
919 ‎‡a  multicomponentpolysaccharideproteinbioconjugationinthedevelopmentofantibacterialglycoconjugatevaccinecandidates‏ ‎‡A  Multicomponent polysaccharide-protein bioconjugation in the development of antibacterial glycoconjugate vaccine candidates.‏ ‎‡9  1‏
919 ‎‡a  multicomponentreactiontoolboxforpeptidemacrocyclizationandstapling‏ ‎‡A  Multicomponent Reaction Toolbox for Peptide Macrocyclization and Stapling‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
996 ‎‡2  BNCHL|10000000000000000287488‏
996 ‎‡2  LC|n 97085088‏
996 ‎‡2  LC|n 96072038‏
996 ‎‡2  LC|no2010080382‏
996 ‎‡2  DNB|1056581786‏
996 ‎‡2  DNB|141140135‏
996 ‎‡2  NUKAT|n 2019157648‏
996 ‎‡2  BNE|XX1631742‏
996 ‎‡2  NTA|330624415‏
996 ‎‡2  LC|no2018101308‏
996 ‎‡2  LC|n 87806433‏
996 ‎‡2  ISNI|0000000079785701‏
996 ‎‡2  RERO|A013609567‏
996 ‎‡2  RERO|A022738872‏
996 ‎‡2  BNE|XX4927027‏
996 ‎‡2  BNE|XX890565‏
996 ‎‡2  DBC|87097991968010‏
996 ‎‡2  DNB|1056205369‏
996 ‎‡2  SUDOC|257448594‏
996 ‎‡2  ISNI|0000000501533367‏
996 ‎‡2  ISNI|0000000119349964‏
996 ‎‡2  DNB|140858075‏
996 ‎‡2  PLWABN|9813202496005606‏
996 ‎‡2  ISNI|0000000060539121‏
996 ‎‡2  NTA|19112916X‏
996 ‎‡2  RERO|A005960871‏
996 ‎‡2  LC|no2018140332‏
996 ‎‡2  LC|no2008181594‏
996 ‎‡2  BIBSYS|9036705‏
996 ‎‡2  BNE|XX5263823‏
996 ‎‡2  ISNI|0000000078897728‏
996 ‎‡2  DNB|1016432909‏
996 ‎‡2  BNE|XX6166044‏
996 ‎‡2  ISNI|0000000040557824‏
996 ‎‡2  LC|no2011043082‏
996 ‎‡2  J9U|987012749468205171‏
996 ‎‡2  BNC|981058610171306706‏
996 ‎‡2  BNE|XX4863964‏
996 ‎‡2  DNB|105656721X‏
996 ‎‡2  SUDOC|140809058‏
996 ‎‡2  LC|no2022023362‏
996 ‎‡2  ISNI|0000000078073980‏
996 ‎‡2  DNB|1206661046‏
996 ‎‡2  ISNI|0000000035181906‏
996 ‎‡2  SUDOC|185208398‏
996 ‎‡2  SUDOC|118111167‏
996 ‎‡2  BNE|XX1709931‏
996 ‎‡2  ISNI|0000000025426439‏
996 ‎‡2  SUDOC|172506603‏
996 ‎‡2  BNE|XX990315‏
996 ‎‡2  BNC|981058512326506706‏
996 ‎‡2  LC|n 91000545‏
996 ‎‡2  LC|ns2019001428‏
996 ‎‡2  LC|n 81100415‏
996 ‎‡2  PLWABN|9810679492405606‏
996 ‎‡2  ISNI|0000000054307367‏
996 ‎‡2  BNE|XX5530847‏
996 ‎‡2  LC|no2011182029‏
996 ‎‡2  NUKAT|n 2013139963‏
996 ‎‡2  DNB|1267850086‏
996 ‎‡2  LC|no2003054409‏
996 ‎‡2  DNB|1057497819‏
996 ‎‡2  NYNYRILM|224310‏
996 ‎‡2  LC|n 2006015125‏
996 ‎‡2  SUDOC|249011905‏
996 ‎‡2  LC|n 89614213‏
996 ‎‡2  ISNI|0000000078734793‏
996 ‎‡2  LC|n 2008031387‏
996 ‎‡2  ISNI|0000000060543913‏
996 ‎‡2  LC|ns2022002270‏
996 ‎‡2  NUKAT|nx2022557353‏
996 ‎‡2  ISNI|0000000381508182‏
996 ‎‡2  NUKAT|nx2023899988‏
996 ‎‡2  LC|no2016133572‏
996 ‎‡2  LC|ns2015002770‏
996 ‎‡2  LC|no2001082470‏
996 ‎‡2  DNB|120325282X‏
996 ‎‡2  LC|n 85102248‏
996 ‎‡2  SUDOC|266627218‏
996 ‎‡2  BNCHL|10000000000000000235988‏
996 ‎‡2  LC|no2001012792‏
996 ‎‡2  LC|no2010165024‏
996 ‎‡2  ISNI|0000000025261216‏
996 ‎‡2  NUKAT|n 2014003062‏
996 ‎‡2  ISNI|0000000038315041‏
996 ‎‡2  DNB|131470973‏
996 ‎‡2  LC|no2020078324‏
996 ‎‡2  LC|no 00031681‏
996 ‎‡2  J9U|987007402211105171‏
996 ‎‡2  ISNI|0000000500098287‏
996 ‎‡2  ISNI|0000000042000907‏
996 ‎‡2  BNE|XX1541216‏
996 ‎‡2  LC|n 2003115999‏
996 ‎‡2  DNB|1057534994‏
996 ‎‡2  LC|n 85133456‏
996 ‎‡2  DNB|1170725678‏
996 ‎‡2  DNB|1188907824‏
996 ‎‡2  NUKAT|n 2020149224‏
996 ‎‡2  LC|no2015073171‏
996 ‎‡2  LIH|LNB:V-77005;=BF‏
996 ‎‡2  LC|no2013038104‏
996 ‎‡2  ISNI|0000000114932691‏
996 ‎‡2  BNC|981058513847706706‏
996 ‎‡2  ISNI|0000000354584948‏
996 ‎‡2  BNE|XX4936847‏
996 ‎‡2  LC|ns2016001889‏
996 ‎‡2  ISNI|0000000079595318‏
996 ‎‡2  ISNI|0000000121477893‏
996 ‎‡2  PLWABN|9811305554905606‏
996 ‎‡2  LC|no2017075152‏
996 ‎‡2  LC|no2006102148‏
996 ‎‡2  J9U|987007397804305171‏
996 ‎‡2  LC|no2003063894‏
996 ‎‡2  DNB|171584260‏
996 ‎‡2  BNCHL|10000000000000000808580‏
996 ‎‡2  LC|nr2006023495‏
996 ‎‡2  ISNI|0000000118724304‏
996 ‎‡2  LC|no2020148702‏
996 ‎‡2  LC|no2017049296‏
996 ‎‡2  NLA|000036449257‏
996 ‎‡2  BNC|981058523307906706‏
996 ‎‡2  LC|no2019041699‏
996 ‎‡2  ISNI|0000000118684613‏
996 ‎‡2  LC|no2024027393‏
996 ‎‡2  CAOONL|ncf13714483‏
996 ‎‡2  NKC|mzk2015895970‏
996 ‎‡2  LC|ns2016004410‏
996 ‎‡2  LC|no 98019642‏
996 ‎‡2  DNB|1201591848‏
996 ‎‡2  LC|ns2022000091‏
996 ‎‡2  SUDOC|195520688‏
996 ‎‡2  NKC|vse2006360706‏
996 ‎‡2  DNB|1153718316‏
996 ‎‡2  DNB|1178179850‏
996 ‎‡2  LC|no2019188453‏
996 ‎‡2  BNF|15537163‏
996 ‎‡2  NSK|000206995‏
996 ‎‡2  BNF|14220910‏
996 ‎‡2  DNB|105668660X‏
996 ‎‡2  SELIBR|350223‏
996 ‎‡2  BNC|981058528414906706‏
996 ‎‡2  LC|no2018009488‏
996 ‎‡2  CAOONL|ncf10724522‏
996 ‎‡2  NTA|339413700‏
996 ‎‡2  ISNI|0000000080492439‏
996 ‎‡2  ISNI|0000000054101078‏
996 ‎‡2  BNCHL|10000000000000000288912‏
996 ‎‡2  DNB|1205097066‏
996 ‎‡2  SUDOC|120027429‏
996 ‎‡2  LC|no2023117142‏
996 ‎‡2  LC|nb2010015675‏
996 ‎‡2  LC|no2022139637‏
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏