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...

4‑Methyl-6,7-dihydro‑4H‑triazolo[4,5‑c]pyridine-Based P2X7 Receptor Antagonists: Optimization of Pharmacokinetic Properties Leading to the Identification of a Clinical Candidate

Journal of medicinal chemistry, 2017-06, Vol.60 (11), p.4559-4572

2017

Volltextzugriff (PDF)

Allyl-Assisted, Cu(I)-Catalyzed Azide–Alkyne Cycloaddition/Allylation Reaction: Assembly of the [1,2,3]Triazolo-4,5,6,7-tetrahydropyridine Core Structure

Journal of organic chemistry, 2015-11, Vol.80 (21), p.11003-11012

2015

Volltextzugriff (PDF)

Gram-Scale Synthesis of a β‑Secretase 1 (BACE 1) Inhibitor

ACS omega, 2017-02, Vol.2 (2), p.397-408

2017

Volltextzugriff (PDF)

The synthesis of 2-amino-4(3H)-quinazolinones and related heterocycles via a mild electrocyclization of aryl guanidines

Tetrahedron letters, 2018-04, Vol.59 (17), p.1623-1626

2018

Volltextzugriff (PDF)

The Exceptional Chelating Ability of Dimethylaluminum Chloride and Methylaluminum Dichloride. The Merged Stereochemical Impact of α- and β-Stereocenters in Chelate-Controlled Carbonyl Addition Reactions with Enolsilane and Hydride Nucleophiles

Journal of the American Chemical Society, 2001-11, Vol.123 (44), p.10840-10852

2001

Volltextzugriff (PDF)

Tetrahydroindazole inhibitors of bacterial type II topoisomerases. Part 2: SAR development and potency against multidrug-resistant strains

Bioorganic & medicinal chemistry letters, 2007-05, Vol.17 (10), p.2718-2722

2007

Volltextzugriff (PDF)

Indole- and benzothiophene-based histamine H3 antagonists

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (21), p.6226-6230

2010

Volltextzugriff (PDF)

Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists I: Discovery of CCKR1 selectivity in a previously CCKR2-selective lead series

Bioorganic & medicinal chemistry letters, 2009-11, Vol.19 (22), p.6373-6375

2009

Volltextzugriff (PDF)

Identification and Optimization of Anthranilic Sulfonamides as Novel, Selective Cholecystokinin-2 Receptor Antagonists

Journal of medicinal chemistry, 2006-10, Vol.49 (21), p.6371-6390

2006

Volltextzugriff (PDF)

Selective Metalation of Functionalized Quinazolines to Enable Discovery and Advancement of Covalent KRAS Inhibitors

Organic process research & development, 2022-10, Vol.26 (10), p.2926-2936

2022

Volltextzugriff (PDF)

Synthesis and solid-phase purification of anthranilic sulfonamides as CCK-2 ligands

Bioorganic & medicinal chemistry letters, 2007-12, Vol.17 (24), p.6905-6909

2007

Volltextzugriff (PDF)

Discovery of potent cholecystokinin-2 receptor antagonists: Elucidation of key pharmacophore elements by X-ray crystallographic and NMR conformational analysis

Bioorganic & medicinal chemistry, 2008-04, Vol.16 (7), p.3917-3925

2008

Volltextzugriff (PDF)

Substituted Azabicyclo[2.2.1]heptanes as Selective Orexin‑1 Antagonists: Discovery of JNJ-54717793

ACS medicinal chemistry letters, 2020-10, Vol.11 (10), p.2002-2009

2020

Volltextzugriff (PDF)

Discovery of a novel series of selective HCN1 blockers

Bioorganic & medicinal chemistry letters, 2011-09, Vol.21 (18), p.5197-5201

2011

Volltextzugriff (PDF)

ChemInform Abstract: Allyl‐Assisted, Cu(I)‐Catalyzed Azide—Alkyne Cycloaddition/Allylation Reaction: Assembly of the [1,2,3]Triazolo‐4,5,6,7‐tetrahydropyridine Core Structure

ChemInform, 2016-02, Vol.47 (11), p.no-no

2016

Volltextzugriff (PDF)

Indole- and benzothiophene-based histamine H 3 antagonists

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (21), p.6226-6230

2010

Volltextzugriff (PDF)

JNJ-26070109 [(R)4-bromo-N-[1-(2,4-difluoro-phenyl)-ethyl]-2-(quinoxaline-5-sulfonylamino)-benzamide]: a novel, potent, and selective cholecystokinin 2 receptor antagonist with good oral bioavailability

The Journal of pharmacology and experimental therapeutics, 2011-07, Vol.338 (1), p.328-336

2011

Volltextzugriff (PDF)

Chelate-controlled carbonyl addition reactions. The exceptional chelating abilityof dimethylaluminum chloride and methylaluminum dichloride

Tetrahedron letters, 1999-06, Vol.40 (24), p.4457-4460

1999

Volltextzugriff (PDF)

Indole- and benzothiophene-based histamine H sub(3 antagonists)

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (21), p.6226-6230

2010

Volltextzugriff (PDF)

Chelation-controlled stannylacetylene additions to β-alkoxy aldehydes promoted by alkylaluminum halide Lewis acids

Tetrahedron letters, 1999-06, Vol.40 (24), p.4461-4462

1999

Volltextzugriff (PDF)

1,2-Diamino-ethane-substituted-6,7,8,9-tetrahydro-5H-pyrimido[4,5-d]azepines as TRPV1 antagonists with improved properties

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (23), p.7142-7146

2010

Volltextzugriff (PDF)

1,2-Diamino-ethane-substituted-6,7,8,9-tetrahydro-5 H-pyrimido[4,5- d]azepines as TRPV1 antagonists with improved properties

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (23), p.7142-7146

2010

Volltextzugriff (PDF)

Chelate control: A pivotal design element in asymmetric synthesis

Allison, Brett Douglas

2001

Volltextzugriff (PDF)

Cuba visit

Teacher (Vancouver), 1999-05, Vol.11 (7), p.8

Brett, Allison

1999

Volltextzugriff (PDF)

1 – 25 von 455

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(404)
Mit Volltextzugriff
(364)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

4‑Methyl-6,7-dihydro‑4H‑triazolo[4,5‑c]pyridine-Based P2X7 Receptor Antagonists: Optimization of Pharmacokinetic Properties Leading to the Identification of a Clinical Candidate

Allyl-Assisted, Cu(I)-Catalyzed Azide–Alkyne Cycloaddition/Allylation Reaction: Assembly of the [1,2,3]Triazolo-4,5,6,7-tetrahydropyridine Core Structure

Gram-Scale Synthesis of a β‑Secretase 1 (BACE 1) Inhibitor

The synthesis of 2-amino-4(3H)-quinazolinones and related heterocycles via a mild electrocyclization of aryl guanidines

The Exceptional Chelating Ability of Dimethylaluminum Chloride and Methylaluminum Dichloride. The Merged Stereochemical Impact of α- and β-Stereocenters in Chelate-Controlled Carbonyl Addition Reactions with Enolsilane and Hydride Nucleophiles

Tetrahydroindazole inhibitors of bacterial type II topoisomerases. Part 2: SAR development and potency against multidrug-resistant strains

Indole- and benzothiophene-based histamine H3 antagonists

Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists I: Discovery of CCKR1 selectivity in a previously CCKR2-selective lead series

Identification and Optimization of Anthranilic Sulfonamides as Novel, Selective Cholecystokinin-2 Receptor Antagonists

Selective Metalation of Functionalized Quinazolines to Enable Discovery and Advancement of Covalent KRAS Inhibitors

Synthesis and solid-phase purification of anthranilic sulfonamides as CCK-2 ligands

Discovery of potent cholecystokinin-2 receptor antagonists: Elucidation of key pharmacophore elements by X-ray crystallographic and NMR conformational analysis

Substituted Azabicyclo[2.2.1]heptanes as Selective Orexin‑1 Antagonists: Discovery of JNJ-54717793

4-Methyl-6,7-dihydro-4 H -triazolo[4,5- c ]pyridine-Based P2X7 Receptor Antagonists: Optimization of Pharmacokinetic Properties Leading to the Identification of a Clinical Candidate

Discovery of a novel series of selective HCN1 blockers

ChemInform Abstract: Allyl‐Assisted, Cu(I)‐Catalyzed Azide—Alkyne Cycloaddition/Allylation Reaction: Assembly of the [1,2,3]Triazolo‐4,5,6,7‐tetrahydropyridine Core Structure

Indole- and benzothiophene-based histamine H 3 antagonists

JNJ-26070109 [(R)4-bromo-N-[1-(2,4-difluoro-phenyl)-ethyl]-2-(quinoxaline-5-sulfonylamino)-benzamide]: a novel, potent, and selective cholecystokinin 2 receptor antagonist with good oral bioavailability

Chelate-controlled carbonyl addition reactions. The exceptional chelating abilityof dimethylaluminum chloride and methylaluminum dichloride

Indole- and benzothiophene-based histamine H sub(3 antagonists)

Chelation-controlled stannylacetylene additions to β-alkoxy aldehydes promoted by alkylaluminum halide Lewis acids

1,2-Diamino-ethane-substituted-6,7,8,9-tetrahydro-5H-pyrimido[4,5-d]azepines as TRPV1 antagonists with improved properties

1,2-Diamino-ethane-substituted-6,7,8,9-tetrahydro-5 H-pyrimido[4,5- d]azepines as TRPV1 antagonists with improved properties

Chelate control: A pivotal design element in asymmetric synthesis

Cuba visit

Suchergebnisse filtern