UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Decarboxylative Anti-Michael Addition to Olefins Mediated by Photoredox Catalysis

Organic letters, 2016-07, Vol.18 (14), p.3494-3497

2016

Volltextzugriff (PDF)

Enantioselective Total Synthesis of Hyperforin

Journal of the American Chemical Society, 2013-01, Vol.135 (2), p.644-647

2013

Volltextzugriff (PDF)

Total Synthesis of (−)-Nemorosone and (+)-Secohyperforin

Organic letters, 2015-07, Vol.17 (14), p.3398-3401

2015

Volltextzugriff (PDF)

Virtual screening to identify potent sepiapterin reductase inhibitors

Bioorganic & medicinal chemistry letters, 2020-01, Vol.30 (2), p.126793-126793, Article 126793

2020

Volltextzugriff (PDF)

Progress in the discovery of small molecule modulators of the Cys-loop superfamily receptors

Bioorganic & medicinal chemistry letters, 2017-08, Vol.27 (15), p.3207-3218

2017

Volltextzugriff (PDF)

Sustainable Practices in Medicinal Chemistry Part 2: Green by Design

Journal of medicinal chemistry, 2017-07, Vol.60 (14), p.5955-5968

2017

Volltextzugriff (PDF)

Sulfonamides as Selective NaV1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity

Journal of medicinal chemistry, 2017-07, Vol.60 (14), p.5990-6017

2017

Volltextzugriff (PDF)

Pharmacological Assessment of Sepiapterin Reductase Inhibition on Tactile Response in the Rat

The Journal of pharmacology and experimental therapeutics, 2019-11, Vol.371 (2), p.476-486

2019

Volltextzugriff (PDF)

Sustainable Practices in Medicinal Chemistry Part 2: Green by Design: Miniperspective

Journal of medicinal chemistry, 2017-07, Vol.60 (14), p.5955-5968

2017

Volltextzugriff (PDF)

High-Throughput Implementation of the NanoBRET Target Engagement Intracellular Kinase Assay to Reveal Differential Compound Engagement by SIK2/3 Isoforms

SLAS discovery, 2020-02, Vol.25 (2), p.215-222

2020

Volltextzugriff (PDF)

Sulfonamides as Selective Na V 1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity

Journal of medicinal chemistry, 2017-07, Vol.60 (14), p.5990-6017

2017

Volltextzugriff (PDF)

Strategic use of nickel(0)-catalyzed enyne–epoxide reductive coupling toward the synthesis of (−)-cyatha-3,12-diene

Tetrahedron, 2009-04, Vol.65 (16), p.3270-3280

2009

Volltextzugriff (PDF)

Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent NaV1.7 inhibitors

MedChemComm, 2017-04, Vol.8 (4), p.744-754

2017

Volltextzugriff (PDF)

Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent Na V 1.7 inhibitors

MedChemComm, 2017-04, Vol.8 (4), p.744-754

2017

Volltextzugriff (PDF)

Strategic use of nickel(0)-catalyzed enyne-epoxide reductive coupling towards the synthesis of (-)-cyatha-3,12-diene

Tetrahedron, 2009-04, Vol.65 (16), p.3270-3280

2009

Volltextzugriff (PDF)

SmI2-Promoted Reformatsky-Type Coupling Reactions in Exceptionally Hindered Contexts

Organic letters, 2008-03, Vol.10 (6), p.1291-1294

2008

Volltextzugriff (PDF)

Abstract A163: Exoribonuclease XRN1 is a therapeutic vulnerability in tumors with intrinsically elevated type I interferon signaling

Molecular cancer therapeutics, 2023-12, Vol.22 (12_Supplement), p.A163-A163

2023

Volltextzugriff (PDF)

Abstract 3337: Inhibition of KIF18A leads to mitotic arrest and robust anti-tumor activity in chromosomally instable tumors

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.3337-3337

2024

Volltextzugriff (PDF)

Abstract B073: Characterization of selective, allosteric inhibitors of human XRN1

Molecular cancer therapeutics, 2023-12, Vol.22 (12_Supplement), p.B073-B073

2023

Volltextzugriff (PDF)

Abstract 1136: Targeting DHX9 inhibition as a novel therapeutic modality in microsatellite instable colorectal cancer

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.1136-1136

2023

Volltextzugriff (PDF)

Strategic use of nickel(0)-catalyzed enyne-epoxide reductive coupling toward the synthesis of (-)-cyatha-3,12-diene: Recent Advances in Synthetic Methodology: Development and Applications

Tetrahedron, 2009, Vol.65 (16)

2009

Volltextzugriff (PDF)

SmI 2 -Promoted Reformatsky-Type Coupling Reactions in Exceptionally Hindered Contexts

Organic letters, 2008-03, Vol.10 (6), p.1291-1294

2008

Volltextzugriff (PDF)

ChemInform Abstract: SmI 2 ‐Promoted Reformatsky‐Type Coupling Reactions in Exceptionally Hindered Contexts

ChemInform, 2008-09, Vol.39 (36)

2008

Volltextzugriff (PDF)

1 – 25 von 63

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(49)

Publikationsform

Sprache

Englisch
(63)

Erscheinungsjahr

n.n

Thema

Science & Technology
(29)
Life Sciences & Biomedicine
(20)
Chemistry
(9)
Humans
(9)
Physical Sciences
(8)
Animals
(6)
Biotechnology & Applied Microbiology
(6)
Genes
(6)
Genomics
(6)
Microbiology
(6)
Proteomics
(6)
Biochemistry & Molecular Biology
(5)
Biodiesel Fuels
(5)
Biotechnology
(5)
Chemistry, Organic
(5)
Genomes
(5)
Male
(5)
Pharmacology & Pharmacy
(5)
Biofuels
(4)
Biomedical And Life Sciences
(4)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Decarboxylative Anti-Michael Addition to Olefins Mediated by Photoredox Catalysis

Enantioselective Total Synthesis of Hyperforin

Total Synthesis of (−)-Nemorosone and (+)-Secohyperforin

Virtual screening to identify potent sepiapterin reductase inhibitors

Progress in the discovery of small molecule modulators of the Cys-loop superfamily receptors

Sustainable Practices in Medicinal Chemistry Part 2: Green by Design

Sulfonamides as Selective NaV1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity

Pharmacological Assessment of Sepiapterin Reductase Inhibition on Tactile Response in the Rat

Sustainable Practices in Medicinal Chemistry Part 2: Green by Design: Miniperspective

High-Throughput Implementation of the NanoBRET Target Engagement Intracellular Kinase Assay to Reveal Differential Compound Engagement by SIK2/3 Isoforms

Sulfonamides as Selective Na V 1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity

Strategic use of nickel(0)-catalyzed enyne–epoxide reductive coupling toward the synthesis of (−)-cyatha-3,12-diene

Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent NaV1.7 inhibitors

Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent Na V 1.7 inhibitors

Strategic use of nickel(0)-catalyzed enyne-epoxide reductive coupling towards the synthesis of (-)-cyatha-3,12-diene

SmI2-Promoted Reformatsky-Type Coupling Reactions in Exceptionally Hindered Contexts

Abstract A163: Exoribonuclease XRN1 is a therapeutic vulnerability in tumors with intrinsically elevated type I interferon signaling

Abstract 3337: Inhibition of KIF18A leads to mitotic arrest and robust anti-tumor activity in chromosomally instable tumors

Abstract B073: Characterization of selective, allosteric inhibitors of human XRN1

Abstract 1136: Targeting DHX9 inhibition as a novel therapeutic modality in microsatellite instable colorectal cancer

Strategic use of nickel(0)-catalyzed enyne-epoxide reductive coupling toward the synthesis of (-)-cyatha-3,12-diene: Recent Advances in Synthetic Methodology: Development and Applications

SmI 2 -Promoted Reformatsky-Type Coupling Reactions in Exceptionally Hindered Contexts

ChemInform Abstract: SmI 2 ‐Promoted Reformatsky‐Type Coupling Reactions in Exceptionally Hindered Contexts

Suchergebnisse filtern