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WKP|Q58305807
(VIAF cluster)
(Authority/Source Record)
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(WKP)Q58305807
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0000-0003-1697-7871
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orcid
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14040402800
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scopus
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35219026200
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scopus
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(OCoLC)Q58305807
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0 |
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Carolina S Marques
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researcher, ORCID id # 0000-0003-1697-7871
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en
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400
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Carolina S Marques
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wetenschapper
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nl
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670
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Author's A simple, highly regioselective, one-pot stereoselective synthesis of tertiary α-hydroxyesters: a tandem oxidation/benzilic ester rearrangement
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670
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Author's Asymmetric catalytic arylation of ethyl glyoxylate using organoboron reagents and Rh
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670
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Author's Asymmetric catalytic arylation of ethyl glyoxylate using organoboron reagents and Rh(i)–phosphane and phosphane–phosphite catalysts
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670
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Author's N-1,2,3-triazole-isatin derivatives for cholinesterase and β-amyloid aggregation inhibition: A comprehensive bioassay study
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670
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Author's New cholinesterase inhibitors for Alzheimer's disease: Structure Activity Studies (SARs) and molecular docking of isoquinolone and azepanone derivatives
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670
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Author's Pd-Catalyzed One-Pot Borylation/Intramolecular Asymmetric Arylation on α-Ketiminoamides: Innovative Approach to Chiral 3-Amino-2-oxindoles
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670
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‡a
Author's The catalytic tandem oxidation/benzilic ester rearrangement
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670
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Author's The catalytic tandem oxidation/benzilic ester rearrangement (BER): insights into reaction mechanism and stereoselectivity
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909
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(scopus) 14040402800
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909
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(scopus) 35219026200
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909
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(orcid) 0000000316977871
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Pd-Catalyzed One-Pot Borylation/Intramolecular Asymmetric Arylation on α-Ketiminoamides: Innovative Approach to Chiral 3-Amino-2-oxindoles
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Asymmetric catalytic arylation of ethyl glyoxylate using organoboron reagents and Rh
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n123triazoleisatinderivativesforcholinesteraseandβamyloidaggregationinhibitionacomprehensivebioassaystudy
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N-1,2,3-triazole-isatin derivatives for cholinesterase and β-amyloid aggregation inhibition: A comprehensive bioassay study
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The catalytic tandem oxidation/benzilic ester rearrangement (BER): insights into reaction mechanism and stereoselectivity
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catalytictandemoxidationbenzilicesterrearrangement
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The catalytic tandem oxidation/benzilic ester rearrangement
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simplehighlyregioselective1potstereoselectivesynthesisoftertiaryαhydroxyestersatandemoxidationbenzilicesterrearrangement
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A simple, highly regioselective, one-pot stereoselective synthesis of tertiary α-hydroxyesters: a tandem oxidation/benzilic ester rearrangement
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asymmetriccatalyticarylationofethylglyoxylateusingorganoboronreagentsandrh1phosphaneandphosphanephosphitecatalysts
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Asymmetric catalytic arylation of ethyl glyoxylate using organoboron reagents and Rh(i)–phosphane and phosphane–phosphite catalysts
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newcholinesteraseinhibitorsforalzheimersdiseasestructureactivitystudiessarsandmoleculardockingofisoquinoloneandazepanonederivatives
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New cholinesterase inhibitors for Alzheimer's disease: Structure Activity Studies (SARs) and molecular docking of isoquinolone and azepanone derivatives
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