A. Palmer

发表

Tetrahydrochromenoimidazoles as potassium-competitive acid blockers (P-CABs): structure-activity relationship of their antisecretory properties and their affinity toward the hERG channel.

D. Hess, W. Simon, P. Zimmermann, 2010, Journal of medicinal chemistry.

5-Substituted 1H-pyrrolo[3,2-b]pyridines as inhibitors of gastric acid secretion.

M. Feth, W. Simon, P. Zimmermann, 2008, Bioorganic & medicinal chemistry.

The Asymmetric Reduction of Heterocyclic Ketones – A Key Step in the Synthesis of Potassium-Competitive Acid Blockers (P-CABs)

A. Zanotti-gerosa, A. Palmer, 2010 .

Preparation of tetrahydroimidazo[2,1-a]isoquinolines and their use as inhibitors of gastric acid secretion.

M. Feth, W. Simon, Hans Christof Holst, 2007, Bioorganic & medicinal chemistry.

New heterocyclic structures from unsaturated aldehyde derivatives. Inhibition of α-L-fucosidases

W. Frey, Han-Qing Dong, V. Jäger, 2000 .

Synthesis and evaluation of 7H-8,9-dihydropyrano[2,3-c]imidazo[1,2-a]pyridines as potassium-competitive acid blockers.

M. Feth, W. Simon, Andreas M Palmer, 2007, Journal of medicinal chemistry.

Pyrrolidine N-Oxides by Stereoselective Addition of Grignard and Lithium Compounds to 4,5-Dideoxy-2,3-O-isopropylidene-D-erythro-4-pentenose N-Benzyl Nitrone and Subsequent Cope−House Cyclization

V. Jäger, A. Palmer, 2001 .

Synthesis of enantiopure 3,6,7,8-tetrahydrochromeno[7,8-d]imidazoles via asymmetric ketone hydrogenation in the presence of RuCl2[Xyl-P-Phos][DAIPEN]

U. Nettekoven, Hans Christof Holst, A. Zanotti-gerosa, 2008 .

Preparation and Biological Evaluation of Pyrrolidinediols and Pyrrolidine N-Oxides from D-Ribose Using the Nitrone Approach

V. Jäger, A. Palmer, 2001 .

Preparation of tricyclic imidazopyridines by asymmetric ketone hydrogenation in the presence of ruthenium phosphino-oxazoline catalyst

U. Nettekoven, A. Palmer, 2007 .

Synthesis and pharmacological evaluation of 5-carboxamide-substituted tetrahydrochromeno[7,8-d]imidazoles

W. Kromer, A. Palmer, G. Münch, 2009 .

Large-Scale Asymmetric Synthesis of the 3,6,7,8-Tetrahydrochromeno[7,8-d]imidazole BYK 405879: A Promising Candidate for the Treatment of Acid-Related Diseases

B. Müller, A. Palmer, M. Webel, 2008 .

Synthesis and pharmacological evaluation of potential metabolites of the potassium-competitive acid blocker BYK 405879

W. Kromer, A. Palmer, G. Münch, 2009 .

Novel imidazo[1,2-a]pyrazine derivatives as potent reversible inhibitors of the gastric H+/K+-ATPase.

W. Simon, P. Zimmermann, Jürgen Volz, 2008, Bioorganic & medicinal chemistry.

Homogenous asymmetric hydrogenation: Recent trends and industrial applications.

A. Zanotti-gerosa, A. Palmer, 2011, Current opinion in drug discovery & development.

Novel indanyl-substituted imidazo[1,2-a]pyridines as potent reversible inhibitors of the gastric H+/K+-ATPase.

M. Feth, W. Simon, P. Zimmermann, 2007, Bioorganic & medicinal chemistry letters.

Preparation of tricyclic imidazopyridines by asymmetric ketone hydrogenation in the presence of RuCl2[(S)-Xyl-P-Phos][(S)-DAIPEN]

H. G. Nedden, A. Zanotti-gerosa, A. Palmer, 2008 .