UB Paderborn / Katalog / Suche / in CDI

1 – 21 von 21

Sortiert nach

Facile preparation of 3-substituted-2,6-difluoropyridines: application to the synthesis of 2,3,6-trisubstituted pyridines

Tetrahedron letters, 2015-10, Vol.56 (44), p.6043-6046

2015

Volltextzugriff (PDF)

Discovery of TAK-925 as a Potent, Selective, and Brain-Penetrant Orexin 2 Receptor Agonist

ACS medicinal chemistry letters, 2022-03, Vol.13 (3), p.457-462

2022

Volltextzugriff (PDF)

Practical application of 3-substituted-2,6-difluoropyridines in drug discovery: Facile synthesis of novel protein kinase C theta inhibitors

Bioorganic & medicinal chemistry letters, 2017-06, Vol.27 (11), p.2497-2501

2017

Volltextzugriff (PDF)

Abstract 2354: Targeted IRAK-M degradation as a novel and efficacious cancer-immunotherapy overcoming innate-driven immunosuppression

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.2354-2354

2019

Volltextzugriff (PDF)

The first C2 selective halide substitution reaction of 2,3-epoxy alcohols by the use of (CH 3O) 3B–MX (X=I, Br, Cl) system

Tetrahedron letters, 2003-12, Vol.44 (50), p.8975-8977

2003

Volltextzugriff (PDF)

Total synthesis of solanoeclepin A

Nature chemistry, 2011-06, Vol.3 (6), p.484

2011

Volltextzugriff (PDF)

Discovery of novel 5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridine derivatives as γ-secretase modulators

Bioorganic & medicinal chemistry letters, 2015-10, Vol.25 (19), p.4245-4249

2015

Volltextzugriff (PDF)

Identification of novel quinazolinedione derivatives as RORγt inverse agonist

Bioorganic & medicinal chemistry, 2018-02, Vol.26 (3), p.721-736

2018

Volltextzugriff (PDF)

Discovery of orally efficacious RORγt inverse agonists. Part 2: Design, synthesis, and biological evaluation of novel tetrahydroisoquinoline derivatives

Bioorganic & medicinal chemistry, 2018-01, Vol.26 (2), p.470-482

2018

Volltextzugriff (PDF)

Parallel fluorescent probe synthesis based on the large-scale preparation of BODIPY FL propionic acid

Bioorganic & medicinal chemistry letters, 2017-03, Vol.27 (5), p.1145-1148

2017

Volltextzugriff (PDF)

Discovery of orally efficacious RORγt inverse agonists, part 1: Identification of novel phenylglycinamides as lead scaffolds

Bioorganic & medicinal chemistry, 2018-01, Vol.26 (2), p.483-500

2018

Volltextzugriff (PDF)

Discovery of spiropiperidine-based potent and selective Orexin-2 receptor antagonists

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6409-6413

2011

Volltextzugriff (PDF)

Design and Synthesis of Conformationally Constrained RORγt Inverse Agonists

ChemMedChem, 2019-11, Vol.14 (22), p.1917-1932

2019

Volltextzugriff (PDF)

Discovery of potent, selective, orally active benzoxazepine-based Orexin-2 receptor antagonists

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6414-6416

2011

Volltextzugriff (PDF)

A Novel Cyclopentene Annulation Method Based on Conjugate Addition Reactions of α-Cyano Carbanion Species

European Journal of Organic Chemistry, 2006-01, Vol.2006 (2), p.328-334

2006

Volltextzugriff (PDF)

ChemInform Abstract: Facile Preparation of 3‐Substituted‐2,6‐difluoropyridines: Application to the Synthesis of 2,3,6‐Trisubstituted Pyridines

ChemInform, 2016-02, Vol.47 (9), p.no-no

2016

Volltextzugriff (PDF)

ChemInform Abstract: Discovery of Spiropiperidine-Based Potent and Selective Orexin-2 Receptor Antagonists

ChemInform, 2012-02, Vol.43 (8), p.no-no

2012

Volltextzugriff (PDF)

ChemInform Abstract: Asymmetric Total Synthesis of Glycinoeclepin A (VIII): Generation of a Novel Bridgehead Anion Species

ChemInform, 2011-02, Vol.42 (5), p.no-no

2011

Volltextzugriff (PDF)

A Novel Cyclopentene Annulation Method Based on Conjugate Addition Reactions of α-Cyano Carbanion Species

ChemInform, 2006-05, Vol.37 (20), p.no-no

2006

Volltextzugriff (PDF)

The First C2 Selective Halide Substitution Reaction of 2,3‐Epoxy Alcohols by the Use of (CH 3 O) 3 B—MX (X: I, Br, Cl) System

ChemInform, 2004-03, Vol.35 (12)

2004

Volltextzugriff (PDF)

The First C2 Selective Halide Substitution Reaction of 2,3-Epoxy Alcohols by the Use of (CH3O)3B-MX (X: I, Br, Cl) System

ChemInform, 2004-03, Vol.35 (12), p.no-no

2004

Volltextzugriff (PDF)

1 – 21 von 21

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(15)
Mit Volltextzugriff
(20)

Publikationsform

Artikel
(21)

Sprache

Englisch
(21)
Japanisch
(4)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Cheminform
(6)
Bioorganic & Medicinal Chemistry Letters
(5)
Bioorganic & Medicinal Chemistry
(3)
Tetrahedron Letters
(2)
Acs Medicinal Chemistry Letters
(1)
Cancer Research
(1)
Chemmedchem
(1)
European Journal Of Organic Chemistry
(1)
Nature Chemistry
(1)

4 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Facile preparation of 3-substituted-2,6-difluoropyridines: application to the synthesis of 2,3,6-trisubstituted pyridines

Discovery of TAK-925 as a Potent, Selective, and Brain-Penetrant Orexin 2 Receptor Agonist

Practical application of 3-substituted-2,6-difluoropyridines in drug discovery: Facile synthesis of novel protein kinase C theta inhibitors

Abstract 2354: Targeted IRAK-M degradation as a novel and efficacious cancer-immunotherapy overcoming innate-driven immunosuppression

The first C2 selective halide substitution reaction of 2,3-epoxy alcohols by the use of (CH 3O) 3B–MX (X=I, Br, Cl) system

Total synthesis of solanoeclepin A

Discovery of novel 5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridine derivatives as γ-secretase modulators

Identification of novel quinazolinedione derivatives as RORγt inverse agonist

Discovery of orally efficacious RORγt inverse agonists. Part 2: Design, synthesis, and biological evaluation of novel tetrahydroisoquinoline derivatives

Parallel fluorescent probe synthesis based on the large-scale preparation of BODIPY FL propionic acid

Discovery of orally efficacious RORγt inverse agonists, part 1: Identification of novel phenylglycinamides as lead scaffolds

Discovery of spiropiperidine-based potent and selective Orexin-2 receptor antagonists

Design and Synthesis of Conformationally Constrained RORγt Inverse Agonists

Discovery of potent, selective, orally active benzoxazepine-based Orexin-2 receptor antagonists

A Novel Cyclopentene Annulation Method Based on Conjugate Addition Reactions of α-Cyano Carbanion Species

ChemInform Abstract: Facile Preparation of 3‐Substituted‐2,6‐difluoropyridines: Application to the Synthesis of 2,3,6‐Trisubstituted Pyridines

ChemInform Abstract: Discovery of Spiropiperidine-Based Potent and Selective Orexin-2 Receptor Antagonists

ChemInform Abstract: Asymmetric Total Synthesis of Glycinoeclepin A (VIII): Generation of a Novel Bridgehead Anion Species

A Novel Cyclopentene Annulation Method Based on Conjugate Addition Reactions of α-Cyano Carbanion Species

The First C2 Selective Halide Substitution Reaction of 2,3‐Epoxy Alcohols by the Use of (CH 3 O) 3 B—MX (X: I, Br, Cl) System

The First C2 Selective Halide Substitution Reaction of 2,3-Epoxy Alcohols by the Use of (CH3O)3B-MX (X: I, Br, Cl) System

Suchergebnisse filtern