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...

DYKAT of Baylis−Hillman Adducts: Concise Total Synthesis of Furaquinocin E

Journal of the American Chemical Society, 2002-10, Vol.124 (39), p.11616-11617

2002

Volltextzugriff (PDF)

Discovery of 3(S)-thiomethyl pyrrolidine ERK inhibitors for oncology

Bioorganic & medicinal chemistry letters, 2018-06, Vol.28 (11), p.2029-2034

2018

Volltextzugriff (PDF)

MK-8353: Discovery of an Orally Bioavailable Dual Mechanism ERK Inhibitor for Oncology

ACS medicinal chemistry letters, 2018-07, Vol.9 (7), p.761-767

2018

Volltextzugriff (PDF)

Efforts towards the optimization of a bi-aryl class of potent IRAK4 inhibitors

Bioorganic & medicinal chemistry letters, 2016-09, Vol.26 (17), p.4250-4255

2016

Volltextzugriff (PDF)

Total Syntheses of Furaquinocin A, B, and E

Journal of the American Chemical Society, 2003-10, Vol.125 (43), p.13155-13164

2003

Volltextzugriff (PDF)

Deracemization of Baylis−Hillman Adducts

Journal of the American Chemical Society, 2000-04, Vol.122 (14), p.3534-3535

2000

Volltextzugriff (PDF)

Enantiospecific Syntheses of (+)-Goniofufurone, (+)-7-epi-Goniofufurone, (+)-Goniobutenolide A, (-)-Goniobutenolide B, (+)-Goniopypyrone, (+)-Altholactone, (+)-Goniotriol, and (+)-7-Acetylgoniotriol

Journal of organic chemistry, 1995-05, Vol.60 (10), p.3121-3130

1995

Volltextzugriff (PDF)

Discovery of a series of potent, orally active α,α-disubstituted piperidine NK1 antagonists

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (21), p.6313-6315

2010

Volltextzugriff (PDF)

Cyclobutane derivatives as potent NK1 selective antagonists

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (14), p.3859-3863

2006

Volltextzugriff (PDF)

Stereochemical Models for the Enantiocontrolled Construction of Fully Functionalized C Rings via Intramolecular Aldolization in Advanced Precursors to Paclitaxel

Journal of organic chemistry, 1998-11, Vol.63 (23), p.8491-8509

1998

Volltextzugriff (PDF)

Discovery of a novel, potent and orally active series of γ-lactams as selective NK1 antagonists

Bioorganic & medicinal chemistry letters, 2008-07, Vol.18 (14), p.4168-4171

2008

Volltextzugriff (PDF)

Enantiospecific syntheses of (3 S,4 R)- and (3 S,4 R,7 S)-diastereoisomers of goniofufurone

Tetrahedron: asymmetry, 1994, Vol.5 (7), p.1269-1274

1994

Volltextzugriff (PDF)

Reversible Charge-Accelerated Oxy-Cope Rearrangements

Journal of organic chemistry, 1998-12, Vol.63 (26), p.9968-9977

1998

Volltextzugriff (PDF)

Stereocontrolled syntheses of (-)-goniofufurone and (-)-8-epi-goniofufurone

Tetrahedron, 1992, Vol.48 (40), p.8659-8666

1992

Volltextzugriff (PDF)

Synthesis of Both Antipodal Forms of 7,7-Dimethylbicyclo[2.2.2]oct-2-en-5-one by Enantiomer Interconversion

Journal of organic chemistry, 1996-01, Vol.61 (1), p.142-145

1996

Volltextzugriff (PDF)

Olefin Cleavage under Osmylation Conditions

Journal of organic chemistry, 1998-10, Vol.63 (22), p.8071-8073

1998

Volltextzugriff (PDF)

Conformation of gem-disubstituted alkylarylpiperidines and their implication in design and synthesis of a conformationally-rigidified NK1 antagonist

Tetrahedron letters, 2013-11, Vol.54 (46), p.6199-6203

2013

Volltextzugriff (PDF)

Application of an S → O Allylic Transposition in the Context of a Bridgehead Olefinic System. New Opportunities for the Structural Modification of Bicyclo[6.2.1]undecanes via Transannular Ring Closure

Journal of organic chemistry, 1998-01, Vol.63 (1), p.129-136

1998

Volltextzugriff (PDF)

Expedient Enantiocontrolled Synthesis of a Tetracyclic Lactone Structurally Related to the Kaurane Diterpenoids

Synlett, 1996-02, Vol.1996 (2), p.129-130

1996

Volltextzugriff (PDF)

Structure-based drug design of clinical compound MK-8353, a novel inhibitor of ERK

Acta crystallographica. Section A, Foundations and advances, 2018-07, Vol.74 (a1), p.a197-a197

2018

Volltextzugriff (PDF)

First total synthesis of potent antitumour agent (+)-goniopypyrone

Tetrahedron letters, 1993, Vol.34 (4), p.691-692

1993

Volltextzugriff (PDF)

Regiocontrolled C-8 Acylation of Castanospermine

Synthetic communications, 1996-06, Vol.26 (11), p.2213-2221

1996

Volltextzugriff (PDF)

Goniofufurone : synthesis and absolute configuration

Journal of the Chemical Society. Chemical communications, 1992 (5), p.432

1992

Volltextzugriff (PDF)

Discovery of a series of potent, orally active alpha , alpha -disubstituted piperidine NK sub(1 antagonists)

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (21), p.6313-6315

2010

Volltextzugriff (PDF)

Discovery of a series of potent, orally active α,α-disubstituted piperidine NK 1 antagonists

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (21), p.6313-6315

2010

Volltextzugriff (PDF)

1 – 25 von 42

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(41)
Dissertationen
(1)

Sprache

Englisch
(42)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

DYKAT of Baylis−Hillman Adducts: Concise Total Synthesis of Furaquinocin E

Discovery of 3(S)-thiomethyl pyrrolidine ERK inhibitors for oncology

MK-8353: Discovery of an Orally Bioavailable Dual Mechanism ERK Inhibitor for Oncology

Efforts towards the optimization of a bi-aryl class of potent IRAK4 inhibitors

Total Syntheses of Furaquinocin A, B, and E

Deracemization of Baylis−Hillman Adducts

Enantiospecific Syntheses of (+)-Goniofufurone, (+)-7-epi-Goniofufurone, (+)-Goniobutenolide A, (-)-Goniobutenolide B, (+)-Goniopypyrone, (+)-Altholactone, (+)-Goniotriol, and (+)-7-Acetylgoniotriol

Discovery of a series of potent, orally active α,α-disubstituted piperidine NK1 antagonists

Cyclobutane derivatives as potent NK1 selective antagonists

Stereochemical Models for the Enantiocontrolled Construction of Fully Functionalized C Rings via Intramolecular Aldolization in Advanced Precursors to Paclitaxel

Discovery of a novel, potent and orally active series of γ-lactams as selective NK1 antagonists

Enantiospecific syntheses of (3 S,4 R)- and (3 S,4 R,7 S)-diastereoisomers of goniofufurone

Reversible Charge-Accelerated Oxy-Cope Rearrangements

Stereocontrolled syntheses of (-)-goniofufurone and (-)-8-epi-goniofufurone

Synthesis of Both Antipodal Forms of 7,7-Dimethylbicyclo[2.2.2]oct-2-en-5-one by Enantiomer Interconversion

Olefin Cleavage under Osmylation Conditions

Conformation of gem-disubstituted alkylarylpiperidines and their implication in design and synthesis of a conformationally-rigidified NK1 antagonist

Application of an S → O Allylic Transposition in the Context of a Bridgehead Olefinic System. New Opportunities for the Structural Modification of Bicyclo[6.2.1]undecanes via Transannular Ring Closure

Expedient Enantiocontrolled Synthesis of a Tetracyclic Lactone Structurally Related to the Kaurane Diterpenoids

Structure-based drug design of clinical compound MK-8353, a novel inhibitor of ERK

First total synthesis of potent antitumour agent (+)-goniopypyrone

Regiocontrolled C-8 Acylation of Castanospermine

Goniofufurone : synthesis and absolute configuration

Discovery of a series of potent, orally active alpha , alpha -disubstituted piperidine NK sub(1 antagonists)

Discovery of a series of potent, orally active α,α-disubstituted piperidine NK 1 antagonists

Suchergebnisse filtern