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...

Pd-Catalyzed N-Arylation of Heteroarylamines

Organic letters, 2002-10, Vol.4 (20), p.3481-3484

2002

Volltextzugriff (PDF)

Efficient Synthesis of NK1 Receptor Antagonist Aprepitant Using a Crystallization-Induced Diastereoselective Transformation

Journal of the American Chemical Society, 2003-02, Vol.125 (8), p.2129-2135

2003

Volltextzugriff (PDF)

Stereoselective Synthesis of a Potent Thrombin Inhibitor by a Novel P2−P3 Lactone Ring Opening

Journal of organic chemistry, 2004-05, Vol.69 (11), p.3620-3627

2004

Volltextzugriff (PDF)

Practical Asymmetric Synthesis of Aprepitant, a Potent Human NK-1 Receptor Antagonist, via a Stereoselective Lewis Acid-Catalyzed Trans Acetalization Reaction

Journal of organic chemistry, 2002-09, Vol.67 (19), p.6743-6747

2002

Volltextzugriff (PDF)

Synthesis of a Tetrahydropyran NK1 Receptor Antagonist via Asymmetric Conjugate Addition

Journal of organic chemistry, 2005-05, Vol.70 (11), p.4409-4413

2005

Volltextzugriff (PDF)

Practical routes to the triarylsulfonyl chloride intermediate of a β3 adrenergic receptor agonist

Tetrahedron, 2003-02, Vol.59 (8), p.1317-1325

2003

Volltextzugriff (PDF)

A very concise synthesis of a potent N-(1,3-thiazol-2-yl)pyridin-2-amine KDR kinase inhibitor

Tetrahedron, 2006-02, Vol.62 (6), p.1110-1115

2006

Volltextzugriff (PDF)

Synthesis of a NO-Releasing Prodrug of Rofecoxib

Journal of organic chemistry, 2006-01, Vol.71 (2), p.480-491

2006

Volltextzugriff (PDF)

Efficient Synthesis of a Highly Selective NPY-5 Receptor Antagonist: A Drug Candidate for the Treatment of Obesity

Organic process research & development, 2006-07, Vol.10 (4), p.822-828

2006

Volltextzugriff (PDF)

Process Development and Large-Scale Synthesis of a PDE4 Inhibitor

Organic process research & development, 2006-01, Vol.10 (1), p.36-45

2006

Volltextzugriff (PDF)

One-Pot Preparation of 7-Hydroxyquinoline

Organic process research & development, 2006-01, Vol.10 (1), p.149-152

2006

Volltextzugriff (PDF)

A regioselective synthesis of 2,4-dialkyl resorcinols

Tetrahedron letters, 2005-03, Vol.46 (10), p.1731-1734

2005

Volltextzugriff (PDF)

Effective use of preparative chiral HPLC in a preclinical drug synthesis

Chirality (New York, N.Y.), 2004, Vol.16 (9), p.609-613

2004

Volltextzugriff (PDF)

A convenient synthesis of 3-aryl-δ-lactones

Tetrahedron letters, 2003-01, Vol.44 (2), p.365-368

2003

Volltextzugriff (PDF)

Practical chemoenzymatic synthesis of a 3-pyridylethanolamino β3 adrenergic receptor agonist

Tetrahedron letters, 1999-09, Vol.40 (37), p.6739-6743

1999

Volltextzugriff (PDF)

Targeting of memory T cells with alefacept in new-onset type 1 diabetes (T1DAL study): 12 month results of a randomised, double-blind, placebo-controlled phase 2 trial

The lancet. Diabetes & endocrinology, 2013-12, Vol.1 (4), p.284-294

2013

Volltextzugriff (PDF)

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

Lancet neurology, 2007-11, Vol.6 (11), p.970-980

2007

Volltextzugriff (PDF)

Stereospecific synthesis of chiral tertiary alkyl-aryl ethers via Mitsunobu reaction with complete inversion of configuration

Tetrahedron letters, 2003-04, Vol.44 (18), p.3609-3611

2003

Volltextzugriff (PDF)

Aluminum-Amine Complexes for the Conversion of Carboxylic Esters to Amides. Application to the Synthesis of LTD4 Antagonist MK-0679

Journal of organic chemistry, 1994-03, Vol.59 (6), p.1231-1233

1994

Volltextzugriff (PDF)

A Highly Efficient Synthesis of Fibrinogen Receptor Antagonist L-734,217 via a Novel Chemoselective Silyl-Mediated Conjugate Addition of δ-Lactams to 4-Vinylpyridine

Journal of organic chemistry, 1996-01, Vol.61 (1), p.215-222

1996

Volltextzugriff (PDF)

Syntheses of morpholine-2,3-diones and 2-hydroxymorpholin-3-ones: intermediates in the synthesis of aprepitant

Tetrahedron letters, 2004-11, Vol.45 (48), p.8917-8920

2004

Volltextzugriff (PDF)

Practical asymmetric synthesis of aklavinone

Tetrahedron, 1984, Vol.40 (22), p.4685-4691

1984

Volltextzugriff (PDF)

Synthesis of a Tetrahydropyran NK 1 Receptor Antagonist via Asymmetric Conjugate Addition

Journal of organic chemistry, 2005-05, Vol.70 (11), p.4409-4413

2005

Volltextzugriff (PDF)

Practical routes to the triarylsulfonyl chloride intermediate of a β 3 adrenergic receptor agonist

Tetrahedron, 2003, Vol.59 (8), p.1317-1325

2003

Volltextzugriff (PDF)

Efficient synthesis of NK(1) receptor antagonist aprepitant using a crystallization-induced diastereoselective transformation

Journal of the American Chemical Society, 2003-02, Vol.125 (8), p.2129-2135

2003

Volltextzugriff (PDF)

1 – 25 von 616

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(572)
Mit Volltextzugriff
(509)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Pd-Catalyzed N-Arylation of Heteroarylamines

Efficient Synthesis of NK1 Receptor Antagonist Aprepitant Using a Crystallization-Induced Diastereoselective Transformation

Stereoselective Synthesis of a Potent Thrombin Inhibitor by a Novel P2−P3 Lactone Ring Opening

Practical Asymmetric Synthesis of Aprepitant, a Potent Human NK-1 Receptor Antagonist, via a Stereoselective Lewis Acid-Catalyzed Trans Acetalization Reaction

Synthesis of a Tetrahydropyran NK1 Receptor Antagonist via Asymmetric Conjugate Addition

Practical routes to the triarylsulfonyl chloride intermediate of a β3 adrenergic receptor agonist

A very concise synthesis of a potent N-(1,3-thiazol-2-yl)pyridin-2-amine KDR kinase inhibitor

Synthesis of a NO-Releasing Prodrug of Rofecoxib

Efficient Synthesis of a Highly Selective NPY-5 Receptor Antagonist: A Drug Candidate for the Treatment of Obesity

Process Development and Large-Scale Synthesis of a PDE4 Inhibitor

One-Pot Preparation of 7-Hydroxyquinoline

A regioselective synthesis of 2,4-dialkyl resorcinols

Effective use of preparative chiral HPLC in a preclinical drug synthesis

A convenient synthesis of 3-aryl-δ-lactones

Practical chemoenzymatic synthesis of a 3-pyridylethanolamino β3 adrenergic receptor agonist

Targeting of memory T cells with alefacept in new-onset type 1 diabetes (T1DAL study): 12 month results of a randomised, double-blind, placebo-controlled phase 2 trial

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

Stereospecific synthesis of chiral tertiary alkyl-aryl ethers via Mitsunobu reaction with complete inversion of configuration

Aluminum-Amine Complexes for the Conversion of Carboxylic Esters to Amides. Application to the Synthesis of LTD4 Antagonist MK-0679

A Highly Efficient Synthesis of Fibrinogen Receptor Antagonist L-734,217 via a Novel Chemoselective Silyl-Mediated Conjugate Addition of δ-Lactams to 4-Vinylpyridine

Syntheses of morpholine-2,3-diones and 2-hydroxymorpholin-3-ones: intermediates in the synthesis of aprepitant

Practical asymmetric synthesis of aklavinone

Synthesis of a Tetrahydropyran NK 1 Receptor Antagonist via Asymmetric Conjugate Addition

Practical routes to the triarylsulfonyl chloride intermediate of a β 3 adrenergic receptor agonist

Efficient synthesis of NK(1) receptor antagonist aprepitant using a crystallization-induced diastereoselective transformation

Suchergebnisse filtern