Science for Life Laboratory
Sweden
Per I. Arvidsson mainly investigates Organic chemistry, Combinatorial chemistry, Aryl, Enantioselective synthesis and Catalysis. Per I. Arvidsson integrates several fields in his works, including Organic chemistry and Rational design. His Combinatorial chemistry study incorporates themes from Gamma secretase, In vitro, Lipophilicity and Plasma protein binding.
His studies deal with areas such as Stereoselectivity, Alcohol, Ligand, Diamine and Phosphine as well as Aryl. His studies in Enantioselective synthesis integrate themes in fields like Nuclear magnetic resonance spectroscopy, Aldehyde and Organic synthesis. The Peptide study which covers Protein secondary structure that intersects with Stereochemistry.
Per I. Arvidsson mostly deals with Organic chemistry, Stereochemistry, Combinatorial chemistry, Catalysis and Enantioselective synthesis. His study in Organocatalysis, Aryl, Tetrahydroisoquinoline, Yield and Aldol reaction are all subfields of Organic chemistry. His Stereochemistry research integrates issues from Amino acid, Protease, Structure–activity relationship and Peptide.
His study in Peptide is interdisciplinary in nature, drawing from both HIV Protease Inhibitor and Cytotoxicity. Per I. Arvidsson combines Combinatorial chemistry and Functional group in his research. The study incorporates disciplines such as Organic synthesis, Enantiomer and Cyclopropanation in addition to Enantioselective synthesis.
Per I. Arvidsson mainly focuses on Organic chemistry, Combinatorial chemistry, Functional group, Pharmacology and Solid-phase synthesis. His Organic chemistry study frequently links to adjacent areas such as Chemical biology. His work carried out in the field of Combinatorial chemistry brings together such families of science as Supercritical fluid chromatography, Lithium amide, Enantioselective synthesis, Diastereomer and Amine gas treating.
His research in Pharmacology intersects with topics in Dimethyl fumarate, Multiple sclerosis and In vitro. His Solid-phase synthesis study incorporates themes from Crystallography, Molecule and Small molecule. In the field of Pharmacokinetics, his study on Active metabolite overlaps with subjects such as Lansoprazole.
His primary areas of investigation include Organic chemistry, Functional group, Combinatorial chemistry, Sulfonamide and Amide. His Organic chemistry study frequently draws connections to adjacent fields such as Chemical biology. Per I. Arvidsson incorporates a variety of subjects into his writings, including Functional group, Fluoride, Warhead, One pot reaction, Aryl and Ligand.
His Combinatorial chemistry study overlaps with Agricultural chemistry and Agrochemical.
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The Outstanding Biological Stability of β‐ and γ‐Peptides toward Proteolytic Enzymes: An In Vitro Investigation with Fifteen Peptidases
Jens Frackenpohl;Per I. Arvidsson;Jürg V. Schreiber;Dieter Seebach.
ChemBioChem (2001)
Rational design of asymmetric organocatalysts-increased reactivity and solvent scope with a tetrazolic acid
Antti Hartikka;Per I Arvidsson.
Tetrahedron-asymmetry (2004)
Mechanistic Insights into the Phosphine-Free RuCp*-Diamine-Catalyzed Hydrogenation of Aryl Ketones: Experimental and Theoretical Evidence for an Alcohol-Mediated Dihydrogen Activation
Christian Hedberg;Klas Källström;Per I. Arvidsson;Peter Brandt.
Journal of the American Chemical Society (2005)
Organocatalytic synthesis of chiral benzopyrans
Thavendran Govender;Leila Hojabri;Firouz Matloubi Moghaddam;Per I. Arvidsson.
Tetrahedron-asymmetry (2006)
On the Antimicrobial and Hemolytic Activities of Amphiphilic β‐Peptides
Per I. Arvidsson;Jens Frackenpohl;Neil S. Ryder;Brigitta Liechty.
ChemBioChem (2001)
Design, machine synthesis, and NMR-solution structure of a β-heptapeptide forming a salt-bridge stabilised 314-helix in methanol and in water
Per I. Arvidsson;Magnus Rueping;Dieter Seebach.
Chemical Communications (2001)
Antibiotic and Hemolytic Activity of a β2/β3 Peptide Capable of Folding into a 12/10-Helical Secondary Structure
Per I. Arvidsson;Neil S. Ryder;H. Markus Weiss;Gerhard Gross.
ChemBioChem (2003)
The outstanding metabolic stability of a 14C‐labeled β‐nonapeptide in rats – in vitro and in vivo pharmacokinetic studies
Hansjörg Wiegand;Bernard Wirz;Alain Schweitzer;Gian P. Camenisch.
Biopharmaceutics & Drug Disposition (2002)
Tetrazolic Acid Functionalized Dihydroindol: Rational Design of a Highly Selective Cyclopropanation Organocatalyst
Antti Hartikka;Per I. Arvidsson.
Journal of Organic Chemistry (2007)
Linear, Peptidase-Resistantβ2/β3-Di- andα/β3-Tetrapeptide Derivatives with Nanomolar Affinities to a Human Somatostatin Receptor, Preliminary Communication
Dieter Seebach;Magnus Rueping;Per I. Arvidsson;Thierry Kimmerlin.
Helvetica Chimica Acta (2001)
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