UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 295

Sortiert nach

Development of Efficient Methods for Accomplishing Cysteine-Free Peptide and Glycopeptide Coupling

Angewandte Chemie (International ed.), 2007-01, Vol.46 (39), p.7383-7387

2007

Link zum Volltext

Verfügbarkeit prüfen

Highly Enantioselective Copper-Catalyzed Conjugate Addition of Diethylzinc to Nitroalkenes

Organic letters, 2004-08, Vol.6 (16), p.2689-2691

2004

Link zum Volltext

Verfügbarkeit prüfen

2-Phenylamino-6-cyano-1H-benzimidazole-based isoform selective casein kinase 1 gamma (CK1γ) inhibitors

Bioorganic & medicinal chemistry letters, 2012-09, Vol.22 (17), p.5392-5395

2012

Link zum Volltext

Verfügbarkeit prüfen

New Biphenol-Based, Fine-Tunable Monodentate Phosphoramidite Ligands for Catalytic Asymmetric Transformations

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (15), p.5411-5416

2004

Link zum Volltext

Verfügbarkeit prüfen

Total Synthesis of (±)-Jiadifenin and Studies Directed to Understanding Its SAR: Probing Mechanistic and Stereochemical Issues in Palladium-Mediated Allylation of Enolate-Like Structures

Journal of the American Chemical Society, 2006-01, Vol.128 (3), p.1016-1022

2006

Link zum Volltext

Verfügbarkeit prüfen

Synthesis of the fucosylated biantennary N-glycan of erythropoietin

Tetrahedron letters, 2006-07, Vol.47 (31), p.5577-5579

2006

Link zum Volltext

Verfügbarkeit prüfen

The Synthesis and Preliminary Biological Evaluation of a Novel Steroid with Neurotrophic Activity: NGA0187

Journal of organic chemistry, 2005-11, Vol.70 (24), p.9849-9856

2005

Link zum Volltext

Verfügbarkeit prüfen

Mature homogeneous erythropoietin building blocks by chemical synthesis: the EPO 22–37 glycopeptide domain presenting the full N-linked dodecasaccharide

Tetrahedron letters, 2006-11, Vol.47 (46), p.8009-8011

2006

Link zum Volltext

Verfügbarkeit prüfen

Design and synthesis of new fluorinated ligands for the rhodium-catalyzed hydroformylation of alkenes in supercritical CO2 and fluorous solvents

Journal of fluorine chemistry, 2001-11, Vol.112 (1), p.101-108

2001

Link zum Volltext

Verfügbarkeit prüfen

Building Complex Glycopeptides: Development of a Cysteine-Free Native Chemical Ligation Protocol

Angewandte Chemie (International ed.), 2006-06, Vol.45 (25), p.4116-4125

2006

Link zum Volltext

Verfügbarkeit prüfen

Development of Novel Dual Binders as Potent, Selective, and Orally Bioavailable Tankyrase Inhibitors

Journal of medicinal chemistry, 2013-12, Vol.56 (24), p.10003-10015

2013

Link zum Volltext

Verfügbarkeit prüfen

Purinylpyridinylamino-based DFG-in/αC-helix-out B-Raf inhibitors: Applying mutant versus wild-type B-Raf selectivity indices for compound profiling

Bioorganic & medicinal chemistry, 2016-05, Vol.24 (10), p.2215-2234

2016

Link zum Volltext

Verfügbarkeit prüfen

Lead Optimization and Modulation of hERG Activity in a Series of Aminooxazoline Xanthene β‑Site Amyloid Precursor Protein Cleaving Enzyme (BACE1) Inhibitors

Journal of medicinal chemistry, 2014-12, Vol.57 (23), p.9796-9810

2014

Link zum Volltext

Verfügbarkeit prüfen

Synthesis of New Chiral Monodentate Phosphite Ligands and Their Use in Catalytic Asymmetric Hydrogenation

Organic letters, 2003-10, Vol.5 (21), p.3831-3834

2003

Link zum Volltext

Verfügbarkeit prüfen

Abstract 1621: Discovery of pyridyl pyrrolopyridinones as potent and selective CK1γ inhibitors

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.1621-1621

2014

Link zum Volltext

Verfügbarkeit prüfen

Biomimetic total synthesis of tricycloillicinone and mechanistic studies toward the rearrangement of prenyl phenyl ethers

Tetrahedron letters, 2008-11, Vol.49 (45), p.6383-6385

2008

Link zum Volltext

Verfügbarkeit prüfen

Corrigendum to “Purinylpyridinylamino-based DFG-in/αC-helix-out B-Raf inhibitors: Applying mutant versus wild-type B-Raf selectivity indices for compound profiling” [Bioorg. Med. Chem. 24 (2016) 2215–2234]

Bioorganic & medicinal chemistry, 2016-07, Vol.24 (13), p.3093-3093

2016

Link zum Volltext

Verfügbarkeit prüfen

Catalytic asymmetric transformations with fine-tunable biphenol-based monodentate ligands

Tetrahedron: asymmetry, 2006-02, Vol.17 (4), p.642-657

2006

Link zum Volltext

Verfügbarkeit prüfen

Development of Efficient Methods for Accomplishing Cysteine-Free Peptide and Glycopeptide Coupling

Angewandte Chemie, 2007-10, Vol.119 (39), p.7527-7531

2007

Link zum Volltext

Verfügbarkeit prüfen

Mature homogeneous erythropoietin-level building blocks by chemical synthesis: the EPO 114–166 glycopeptide domain, presenting the O-linked glycophorin

Tetrahedron letters, 2006-11, Vol.47 (46), p.8013-8016

2006

Link zum Volltext

Verfügbarkeit prüfen

Reiterative cysteine-based coupling leading to complex, homogeneous glycopeptides

Tetrahedron letters, 2006-07, Vol.47 (29), p.5219-5223

2006

Link zum Volltext

Verfügbarkeit prüfen

2-Phenylamino-6-cyano-1H-benzimidazole-based isoform selective casein kinase 1 gamma (CK1γ) inhibitors

Bioorganic & medicinal chemistry letters, 2012-09, Vol.22 (17)

2012

Link zum Volltext

Verfügbarkeit prüfen

Structure-Based Design of Potent and Selective CK1γ Inhibitors

ACS medicinal chemistry letters, 2012-12, Vol.3 (12), p.1059-1064

2012

Link zum Volltext

Verfügbarkeit prüfen

Development of Efficient Methods for Accomplishing Cysteine‐Free Peptide and Glycopeptide Coupling

Angewandte Chemie, 2007-10, Vol.119 (39), p.7527-7531

2007

Link zum Volltext

Verfügbarkeit prüfen

Building Complex Glycopeptides: Development of a Cysteine‐Free Native Chemical Ligation Protocol

Angewandte Chemie, 2006-06, Vol.118 (25), p.4222-4231

2006

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 295

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(263)
Mit Volltextzugriff
(280)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(226)
Life Sciences & Biomedicine
(114)
Physical Sciences
(94)
Technology
(76)
Chemistry
(63)
Humans
(47)
Engineering
(37)
Materials Science
(33)
Environmental Sciences & Ecology
(25)
Environmental Sciences
(24)
Chemistry, Multidisciplinary
(23)
Science & Technology - Other Topics
(23)
Physics
(22)
Chemistry, Physical
(21)
Materials Science, Multidisciplinary
(21)
Animals
(20)
Oncology
(19)
Male
(16)
Female
(15)
Mice
(14)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(16)
... seit 30 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Development of Efficient Methods for Accomplishing Cysteine-Free Peptide and Glycopeptide Coupling

Highly Enantioselective Copper-Catalyzed Conjugate Addition of Diethylzinc to Nitroalkenes

2-Phenylamino-6-cyano-1H-benzimidazole-based isoform selective casein kinase 1 gamma (CK1γ) inhibitors

New Biphenol-Based, Fine-Tunable Monodentate Phosphoramidite Ligands for Catalytic Asymmetric Transformations

Total Synthesis of (±)-Jiadifenin and Studies Directed to Understanding Its SAR: Probing Mechanistic and Stereochemical Issues in Palladium-Mediated Allylation of Enolate-Like Structures

Synthesis of the fucosylated biantennary N-glycan of erythropoietin

The Synthesis and Preliminary Biological Evaluation of a Novel Steroid with Neurotrophic Activity: NGA0187

Mature homogeneous erythropoietin building blocks by chemical synthesis: the EPO 22–37 glycopeptide domain presenting the full N-linked dodecasaccharide

Design and synthesis of new fluorinated ligands for the rhodium-catalyzed hydroformylation of alkenes in supercritical CO2 and fluorous solvents

Building Complex Glycopeptides: Development of a Cysteine-Free Native Chemical Ligation Protocol

Development of Novel Dual Binders as Potent, Selective, and Orally Bioavailable Tankyrase Inhibitors

Purinylpyridinylamino-based DFG-in/αC-helix-out B-Raf inhibitors: Applying mutant versus wild-type B-Raf selectivity indices for compound profiling

Lead Optimization and Modulation of hERG Activity in a Series of Aminooxazoline Xanthene β‑Site Amyloid Precursor Protein Cleaving Enzyme (BACE1) Inhibitors

Synthesis of New Chiral Monodentate Phosphite Ligands and Their Use in Catalytic Asymmetric Hydrogenation

Abstract 1621: Discovery of pyridyl pyrrolopyridinones as potent and selective CK1γ inhibitors

Biomimetic total synthesis of tricycloillicinone and mechanistic studies toward the rearrangement of prenyl phenyl ethers

Corrigendum to “Purinylpyridinylamino-based DFG-in/αC-helix-out B-Raf inhibitors: Applying mutant versus wild-type B-Raf selectivity indices for compound profiling” [Bioorg. Med. Chem. 24 (2016) 2215–2234]

Catalytic asymmetric transformations with fine-tunable biphenol-based monodentate ligands

Development of Efficient Methods for Accomplishing Cysteine-Free Peptide and Glycopeptide Coupling

Mature homogeneous erythropoietin-level building blocks by chemical synthesis: the EPO 114–166 glycopeptide domain, presenting the O-linked glycophorin

Reiterative cysteine-based coupling leading to complex, homogeneous glycopeptides

2-Phenylamino-6-cyano-1H-benzimidazole-based isoform selective casein kinase 1 gamma (CK1γ) inhibitors

Structure-Based Design of Potent and Selective CK1γ Inhibitors

Development of Efficient Methods for Accomplishing Cysteine‐Free Peptide and Glycopeptide Coupling

Building Complex Glycopeptides: Development of a Cysteine‐Free Native Chemical Ligation Protocol

Suchergebnisse filtern