S. Karlström

发表

Di-2-pyridylmethylamine-based palladium complexes as new catalysts for Heck, Suzuki, and Sonogashira reactions in organic and aqueous solvents.

L. Falvello, C. Nájera, J. Gil-Moltó, 2003, Organic letters.

Discovery of AZD3839, a potent and selective BACE1 clinical candidate for the treatment of Alzheimer’s Disease*

B. Ploeger, S. Eketjäll, B. Swahn, 2012 .

Di(2-pyridyl)methylamine–palladium dichloride complex covalently anchored to a styrene-maleic anhydride co-polymer as recoverable catalyst for C–C cross-coupling reactions in water

C. Nájera, J. Gil-Moltó, S. Karlström, 2005 .

Biotransformation of Two b -Secretase Inhibitors Including Ring Opening and Contraction of a Pyrimidine Ring s

J. Holenz, J. Malmquist, B. Swahn, 2013 .

Substituted 7-amino-5-thio-thiazolo[4,5-d]pyrimidines as potent and selective antagonists of the fractalkine receptor (CX3CR1).

V. Ivanov, L. Vares, P. Svensson, 2013, Journal of medicinal chemistry.

Suzuki–Miyaura and Related Cross‐Couplings in Aqueous Solvents Catalyzed by Di(2‐pyridyl)methylamine‐Palladium Dichloride Complexes

C. Nájera, J. Gil-Moltó, S. Karlström, 2004 .

Discovery of USP7 Small-Molecule Allosteric Inhibitors.

M. Rapp, D. Derbyshire, O. Engström, 2020, Bioorganic & medicinal chemistry letters.

Discovery of AZD3839, a Potent and Selective BACE1 Inhibitor Clinical Candidate for the Treatment of Alzheimer Disease*

Britt-Marie Swahn, Bart Ploeger, Tjerk Bueters, 2012, The Journal of Biological Chemistry.

New aminoimidazoles as β-secretase (BACE-1) inhibitors showing amyloid-β (Aβ) lowering in brain.

S. Eketjäll, B. Swahn, K. Kolmodin, 2012, Journal of medicinal chemistry.

AZ-4217: A High Potency BACE Inhibitor Displaying Acute Central Efficacy in Different In Vivo Models and Reduced Amyloid Deposition in Tg2576 Mice

S. Eketjäll, B. Swahn, K. Kolmodin, 2013, The Journal of Neuroscience.

Design and synthesis of β-site amyloid precursor protein cleaving enzyme (BACE1) inhibitors with in vivo brain reduction of β-amyloid peptides.

Britt-Marie Swahn, Johan Lindström, Stefan Berg, 2012, Journal of medicinal chemistry.

Biotransformation of Two β-Secretase Inhibitors Including Ring Opening and Contraction of a Pyrimidine Ring

J. Holenz, J. Malmquist, B. Swahn, 2013, Drug Metabolism and Disposition.

Substituted 7-amino-5-thio-thiazolo[4,5-d]pyrimidines as potent and selective antagonists of the fractalkine receptor (CX3CR1).

V. Ivanov, L. Vares, E. Jerning, 2013, Journal of medicinal chemistry.