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...

Cross-Coupling Methods for the Large-Scale Preparation of an Imidazole−Thienopyridine: Synthesis of [2-(3-Methyl-3H-imidazol-4-yl)- thieno[3,2-b]pyridin-7-yl]-(2-methyl-1H-indol-5-yl)-amine

Organic process research & development, 2003-09, Vol.7 (5), p.676-683

2003

Volltextzugriff (PDF)

Evaluation of Kilogram-Scale Sonagashira, Suzuki, and Heck Coupling Routes to Oncology Candidate CP-724,714

Organic process research & development, 2005-07, Vol.9 (4), p.440-450

2005

Volltextzugriff (PDF)

Pharmaceutical impurity identification: A case study using a multidisciplinary approach

Journal of pharmaceutical sciences, 2004-09, Vol.93 (9), p.2296-2309

2004

Volltextzugriff (PDF)

Pyrroles as terminators in cationic cyclizations. The preparation of 5,6,7,8-tetrahydroindolizidines and 6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]azepines

Journal of organic chemistry, 1987-03, Vol.52 (5), p.819-827

1987

Volltextzugriff (PDF)

Streamlined Processes for the Synthesis of a Farnesyl Transferase Inhibitor Drug Candidate

Organic process research & development, 2004-07, Vol.8 (4), p.643-650

2004

Volltextzugriff (PDF)

Furan-Terminated N-Acyliminium Ion Initiated Cyclizations in Alkaloid Synthesis

Journal of organic chemistry, 1998-10, Vol.63 (20), p.6914-6928

1998

Volltextzugriff (PDF)

A Reliable Multikilogram-Scale Synthesis of 2-Acetamido-5-Vinylpyridine Using Catalytic BINAP in a Modified Heck Reaction

Organic process research & development, 2002-01, Vol.6 (1), p.67-69

2002

Volltextzugriff (PDF)

A significant new product from the addition of dichlorocarbene to tetraphenylcyclone

Tetrahedron letters, 1983, Vol.24 (45), p.4891-4894

1983

Volltextzugriff (PDF)

Process Research and Scale-Up for a β-3 Adrenergic Receptor Agonist

Organic process research & development, 2004-07, Vol.8 (4), p.583-586

2004

Volltextzugriff (PDF)

Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro- s-indacen-4-yl)-3-[4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Anti-inflammatory Agent

Synthetic communications, 2003-07, Vol.33 (12), p.2029-2043

2003

Volltextzugriff (PDF)

PREPARATION OF 4-CHLORO-2-THIOPHENECARBOXYLIC ACID via SELECTIVE BISULFITE SALT ADDITION PROCEDURE

Organic preparations and procedures international, 1995-04, Vol.27 (2), p.233-236

1995

Volltextzugriff (PDF)

ChemInform Abstract: A SIGNIFICANT NEW PRODUCT FROM THE ADDITION OF DICHLOROCARBENE TO TETRAPHENYLCYCLONE

Chemischer Informationsdienst, 1984-02, Vol.15 (8)

1984

Volltextzugriff (PDF)

A PRACTICAL SYNTHESIS OF 4-BROMO-2-CYANO-3-METHYL-2-BUTENENITRILE

Organic preparations and procedures international, 1995-12, Vol.27 (6), p.695-697

1995

Volltextzugriff (PDF)

ChemInform Abstract: Pyrroles as Terminators in Cationic Cyclizations. The Preparation of 5,6,7,8‐Tetrahydroindolizidines and 6,7,8,9‐Tetrahydro‐5H‐pyrrolo‐(1,2‐a)azepines

ChemInform, 1987-10, Vol.18 (41), p.no-no

1987

Volltextzugriff (PDF)

ChemInform Abstract: Furan-Terminated N-Acyliminium Ion Initiated Cyclizations in Alkaloid Synthesis

ChemInform, 1999-03, Vol.30 (10), p.no-no

1999

Volltextzugriff (PDF)

ChemInform Abstract: Preparation of 4-Chloro-2-thiophenecarboxylic Acid (III) via Selective Bisulfite Salt Addition Procedure

ChemInform, 1995-08, Vol.26 (35), p.no-no

1995

Volltextzugriff (PDF)

ChemInform Abstract: A Practical Synthesis of 4-Bromo-2-cyano-3-methyl-2-butenenitrile

ChemInform, 1996-04, Vol.27 (18), p.no-no

1996

Volltextzugriff (PDF)

Spatial Variability in Growth-Increment Chronologies of Long-Lived Freshwater Mussels: Implications for Climate Impacts and Reconstructions

Écoscience (Sainte-Foy), 2010-09, Vol.17 (3), p.240-250

2010

Volltextzugriff (PDF)

Early Process Development of PF-07054894, a Squaramide-Based Antagonist of C–C Chemokine Receptor Type 6 (CCR6)

Organic process research & development, 2024-06, Vol.28 (6), p.2247-2259

2024

Volltextzugriff (PDF)

Discovery of Two Clinical Histamine H 3 Receptor Antagonists: trans - N -Ethyl-3-fluoro-3-[3-fluoro-4-(pyrrolidinylmethyl)phenyl]cyclobutanecarboxamide (PF-03654746) and trans -3-Fluoro-3-[3-fluoro-4-(pyrrolidin-1-ylmethyl)phenyl]- N -(2-methylpropyl)cyclobutanecarboxamide (PF-03654764)

Journal of medicinal chemistry, 2011-11, Vol.54 (21), p.7602-7620

2011

Volltextzugriff (PDF)

Process Development of a Second Generation β‑Amyloid-Cleaving Enzyme InhibitorImproving the Robustness of a Halogen-Metal Exchange Using Continuous Stirred-Tank Reactors

Organic process research & development, 2021-06, Vol.25 (6), p.1440-1453

2021

Volltextzugriff (PDF)

Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro-s-indacen-4-yl)-3- [4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Antiinflammatory Agent

ChemInform, 2003-10, Vol.34 (43), p.no-no

2003

Volltextzugriff (PDF)

1 – 24 von 24

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(18)
Mit Volltextzugriff
(20)

Publikationsform

Artikel
(24)

Sprache

Englisch
(24)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Cross-Coupling Methods for the Large-Scale Preparation of an Imidazole−Thienopyridine: Synthesis of [2-(3-Methyl-3H-imidazol-4-yl)- thieno[3,2-b]pyridin-7-yl]-(2-methyl-1H-indol-5-yl)-amine

Evaluation of Kilogram-Scale Sonagashira, Suzuki, and Heck Coupling Routes to Oncology Candidate CP-724,714

Pharmaceutical impurity identification: A case study using a multidisciplinary approach

Pyrroles as terminators in cationic cyclizations. The preparation of 5,6,7,8-tetrahydroindolizidines and 6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]azepines

Streamlined Processes for the Synthesis of a Farnesyl Transferase Inhibitor Drug Candidate

Furan-Terminated N-Acyliminium Ion Initiated Cyclizations in Alkaloid Synthesis

A Reliable Multikilogram-Scale Synthesis of 2-Acetamido-5-Vinylpyridine Using Catalytic BINAP in a Modified Heck Reaction

A significant new product from the addition of dichlorocarbene to tetraphenylcyclone

Process Research and Scale-Up for a β-3 Adrenergic Receptor Agonist

Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro- s-indacen-4-yl)-3-[4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Anti-inflammatory Agent

PREPARATION OF 4-CHLORO-2-THIOPHENECARBOXYLIC ACID via SELECTIVE BISULFITE SALT ADDITION PROCEDURE

ChemInform Abstract: A SIGNIFICANT NEW PRODUCT FROM THE ADDITION OF DICHLOROCARBENE TO TETRAPHENYLCYCLONE

A PRACTICAL SYNTHESIS OF 4-BROMO-2-CYANO-3-METHYL-2-BUTENENITRILE

ChemInform Abstract: Pyrroles as Terminators in Cationic Cyclizations. The Preparation of 5,6,7,8‐Tetrahydroindolizidines and 6,7,8,9‐Tetrahydro‐5H‐pyrrolo‐(1,2‐a)azepines

ChemInform Abstract: Furan-Terminated N-Acyliminium Ion Initiated Cyclizations in Alkaloid Synthesis

ChemInform Abstract: Preparation of 4-Chloro-2-thiophenecarboxylic Acid (III) via Selective Bisulfite Salt Addition Procedure

ChemInform Abstract: A Practical Synthesis of 4-Bromo-2-cyano-3-methyl-2-butenenitrile

Spatial Variability in Growth-Increment Chronologies of Long-Lived Freshwater Mussels: Implications for Climate Impacts and Reconstructions

Early Process Development of PF-07054894, a Squaramide-Based Antagonist of C–C Chemokine Receptor Type 6 (CCR6)

Discovery of Two Clinical Histamine H 3 Receptor Antagonists: trans - N -Ethyl-3-fluoro-3-[3-fluoro-4-(pyrrolidinylmethyl)phenyl]cyclobutanecarboxamide (PF-03654746) and trans -3-Fluoro-3-[3-fluoro-4-(pyrrolidin-1-ylmethyl)phenyl]- N -(2-methylpropyl)cyclobutanecarboxamide (PF-03654764)

Process Development of a Second Generation β‑Amyloid-Cleaving Enzyme InhibitorImproving the Robustness of a Halogen-Metal Exchange Using Continuous Stirred-Tank Reactors

Discovery of two clinical histamine H(3) receptor antagonists: trans-N-ethyl-3-fluoro-3-[3-fluoro-4-(pyrrolidinylmethyl)phenyl]cyclobutanecarboxamide (PF-03654746) and trans-3-fluoro-3-[3-fluoro-4-(pyrrolidin-1-ylmethyl)phenyl]-N-(2-methylpropyl)cyclobutanecarboxamide (PF-03654764)

Discovery of Two Clinical Histamine H3 Receptor Antagonists: trans-N-Ethyl-3-fluoro-3-[3-fluoro-4-(pyrrolidinylmethyl)phenyl]cyclobutanecarboxamide (PF-03654746) and trans-3-Fluoro-3-[3-fluoro-4-(pyrrolidin-1-ylmethyl)phenyl]-N-(2-methylpropyl)cyclobutanecarboxamide (PF-03654764)

Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro-s-indacen-4-yl)-3- [4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Antiinflammatory Agent

Suchergebnisse filtern