UB Paderborn / Katalog / Suche / in CDI

Identification of KasA as the cellular target of an anti-tubercular scaffold

Nature communications, 2016-09, Vol.7 (1), p.12581-12581, Article 12581

2016

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Enantioselective [4 + 2] Cycloadditions of o-Quinone Methides: Total Synthesis of (+)-Mimosifoliol and Formal Synthesis of (+)-Tolterodine

Journal of organic chemistry, 2004-12, Vol.69 (26), p.9196-9203

2004

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Discovery and Characterization of GSK2801, a Selective Chemical Probe for the Bromodomains BAZ2A and BAZ2B

Journal of medicinal chemistry, 2016-02, Vol.59 (4), p.1410-1424

2016

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Total synthesis of (−)-bis-8,8′-catechinylmethane isolated from cocoa liquor

Tetrahedron letters, 2014-04, Vol.55 (15), p.2484-2486

2014

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(±)-Diinsininone: made nature's way

Tetrahedron, 2006-05, Vol.62 (22), p.5298-5307

2006

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Novel Antitubercular 6‑Dialkylaminopyrimidine Carboxamides from Phenotypic Whole-Cell High Throughput Screening of a SoftFocus Library: Structure–Activity Relationship and Target Identification Studies

Journal of medicinal chemistry, 2017-12, Vol.60 (24), p.10118-10134

2017

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Essential but Not Vulnerable: Indazole Sulfonamides Targeting Inosine Monophosphate Dehydrogenase as Potential Leads against Mycobacterium tuberculosis

ACS infectious diseases, 2017-01, Vol.3 (1), p.18-33

2017

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1037. Qualitative Findings from a Hybrid III Implementation-Effectiveness Study to Explore Perspectives of Health-care Staff on Early Implementation of Cabotegravir and Rilpivirine Long Acting (CAB+RPV LA) Injectable HIV treatment in the US (CUSTOMIZE)

Open forum infectious diseases, 2020-12, Vol.7 (Supplement_1), p.S549-S549

2020

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The Discovery of Novel Antimalarial Aminoxadiazoles as a Promising Nonendoperoxide Scaffold

Journal of medicinal chemistry, 2017-08, Vol.60 (16), p.6880-6896

2017

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Correction to The Discovery of Novel Antimalarial Aminoxadiazoles as a Promising Nonendoperoxide Scaffold

Journal of medicinal chemistry, 2017-12, Vol.60 (23), p.9911-9911

2017

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Collaborative approaches for Target ID in neglected diseases: identifying new antimalarial targets

Malaria journal, 2014-09, Vol.13 (S1), p.54-54, Article P54

2014

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Rapid Syntheses of Benzopyrans from o-OBOC Salicylaldehydes and Salicyl alcohols: A Three-Component Reaction

Journal of organic chemistry, 2002-10, Vol.67 (20), p.6911-6915

2002

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Diastereoselective [4+2] Reactions of o-Quinone Methides with a Chiral Enol Ether: Asymmetric Synthesis of (+)-R-Mimosifoliol

Synlett, 2004-05, Vol.2004 (6), p.1101-1103

2004

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Enantioselective [4 + 2] Cycloadditions of o-Quinone Methides: Total Synthesis of (+)-Mimosifoliol and Formal Synthesis of (+)-Tolterodine

Journal of organic chemistry, 2005-04, Vol.70 (8), p.3342-3342

2005

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General method for the construction of type-A proanthocyanidins: Synthesis of racemic-diinsininone

Selenski, Carolyn

2006

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General method for the construction of type-A proanthocyanidins: Synthesis of racemic-diinsininone

Selenski, Carolyn

2006

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ProQuest

ChemInform Abstract: Total Synthesis of (-)-Bis-8,8′-catechinylmethane Isolated from Cocoa Liquor

ChemInform, 2014-09, Vol.45 (38), p.no-no

2014

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Enantioselective [4 + 2] Cycloadditions of o-Quinone Methides: Total Synthesis of (+)-Mimosifoliol (I) and Formal Synthesis of (+)-Tolterodine (II)

ChemInform, 2005-05, Vol.36 (19), p.no-no

2005

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Rapid Syntheses of Benzopyrans from o-OBOC Salicylaldehydes and Salicyl Alcohols: A Three-Component Reaction

ChemInform, 2003-03, Vol.34 (10), p.no-no

2003

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Identification of KasA as the cellular target of an anti-tubercular scaffold

Enantioselective [4 + 2] Cycloadditions of o-Quinone Methides: Total Synthesis of (+)-Mimosifoliol and Formal Synthesis of (+)-Tolterodine

Discovery and Characterization of GSK2801, a Selective Chemical Probe for the Bromodomains BAZ2A and BAZ2B

Total synthesis of (−)-bis-8,8′-catechinylmethane isolated from cocoa liquor

(±)-Diinsininone: made nature's way

Novel Antitubercular 6‑Dialkylaminopyrimidine Carboxamides from Phenotypic Whole-Cell High Throughput Screening of a SoftFocus Library: Structure–Activity Relationship and Target Identification Studies

Essential but Not Vulnerable: Indazole Sulfonamides Targeting Inosine Monophosphate Dehydrogenase as Potential Leads against Mycobacterium tuberculosis

1037. Qualitative Findings from a Hybrid III Implementation-Effectiveness Study to Explore Perspectives of Health-care Staff on Early Implementation of Cabotegravir and Rilpivirine Long Acting (CAB+RPV LA) Injectable HIV treatment in the US (CUSTOMIZE)

The Discovery of Novel Antimalarial Aminoxadiazoles as a Promising Nonendoperoxide Scaffold

Correction to The Discovery of Novel Antimalarial Aminoxadiazoles as a Promising Nonendoperoxide Scaffold

Collaborative approaches for Target ID in neglected diseases: identifying new antimalarial targets

Rapid Syntheses of Benzopyrans from o-OBOC Salicylaldehydes and Salicyl alcohols: A Three-Component Reaction

Diastereoselective [4+2] Reactions of o-Quinone Methides with a Chiral Enol Ether: Asymmetric Synthesis of (+)-R-Mimosifoliol

Enantioselective [4 + 2] Cycloadditions of o-Quinone Methides: Total Synthesis of (+)-Mimosifoliol and Formal Synthesis of (+)-Tolterodine

General method for the construction of type-A proanthocyanidins: Synthesis of racemic-diinsininone

General method for the construction of type-A proanthocyanidins: Synthesis of racemic-diinsininone

ChemInform Abstract: Total Synthesis of (-)-Bis-8,8′-catechinylmethane Isolated from Cocoa Liquor

Enantioselective [4 + 2] Cycloadditions of o-Quinone Methides: Total Synthesis of (+)-Mimosifoliol (I) and Formal Synthesis of (+)-Tolterodine (II)

Rapid Syntheses of Benzopyrans from o-OBOC Salicylaldehydes and Salicyl Alcohols: A Three-Component Reaction

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