L. Thunberg

发表

Unexpected carbonate salt formation during isolation of an enantiopure intermediate by supercritical fluid chromatography.

Anna-Carin C. Carlsson, H. Leek, Anna C. Jonson, 2020, Journal of chromatography. A.

Selectivity limits of and opportunities for ion pair chromatographic separation of oligonucleotides.

T. Fornstedt, Eivor Örnskov, A. Dahlén, 2021, Journal of chromatography. A.

Discovery of the first nonpeptide agonist of the GPR14/urotensin-II receptor: 3-(4-chlorophenyl)-3-(2- (dimethylamino)ethyl)isochroman-1-one (AC-7954).

U. Hacksell, D. Weiner, M. Brann, 2002, Journal of medicinal chemistry.

AZD0284, a Potent, Selective, and Orally Bioavailable Inverse Agonist of Retinoic Acid Receptor-Related Orphan Receptor C2.

R. Pehrson, Yafeng Xue, F. Narjes, 2021, Journal of medicinal chemistry.

Saccharin Aza Bioisosteres-Synthesis and Preclinical Property Comparisons.

R. Lewis, M. A. Hayes, M. Lepistö, 2017, ACS medicinal chemistry letters.

Asymmetric cycloaddition routes to both enantiomers of trans-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxylic acid

S. Allenmark, L. Thunberg, 2003 .

Resolution studies on two regioisomeric chiral stationary phases: effects from reversed orientation of an amide group.

S. Allenmark, L. Thunberg, 2004, Journal of chromatography. A.

Chiral selectors based on C2-symmetric dicarboxylic acids

U. Skogsberg, S. Allenmark, L. Thunberg, 2000 .

Strategy for large-scale isolation of enantiomers in drug discovery.

H. Leek, Magnus Klarqvist, Kristina Öhlén, 2017, Drug discovery today.

Comparative study of coated and immobilized polysaccharide-based chiral stationary phases and their applicability in the resolution of enantiomers.

J. Hashemi, S. Andersson, L. Thunberg, 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Chiral 1,5-disubstituted 1,2,3-triazoles - versatile tools for foldamers and peptidomimetic applications.

T. Beke-Somfai, I. Szigyártó, N. Kann, 2020, Organic & biomolecular chemistry.

Resolution and Chiroptical Characterization of Two 1,8-Bridged Naphthalene Systems: Naphtho[1,8-cd]-1,2-dithiole 1-Oxide and 2H-Naphtho[1,8-bc]thiophene 1-Oxide.

T. Shono, H. Toftlund, J. Oxelbark, 1999 .

Analytical and preparative separation of phosphorothioated oligonucleotides: columns and ion-pair reagents

T. Fornstedt, Eivor Örnskov, Martin Enmark, 2019, Analytical and Bioanalytical Chemistry.

Potent and Orally Bioavailable Inverse Agonists of RORγt Resulting from Structure-Based Design.

Yafeng Xue, F. Narjes, Elisabeth Bäck, 2018, Journal of medicinal chemistry.

Evaluation of two pairs of chiral stationary phases: effects from the length of the achiral spacers.

F. Ek, Annika Friberg, T. Frejd, 2004, Chirality.

Evaluation of a chiral stationary phase derived from a simple Diels-Alder reaction.

S. Allenmark, L. Thunberg, 2003, Chirality.

Potent and Orally Bioavailable Inverse Agonists of RORγt Resulting from Structure-Based Design.

Yafeng Xue, F. Narjes, Elisabeth Bäck, 2018, Journal of medicinal chemistry.

A hierarchical screening approach to enantiomeric separation.

Jonna C. Stålring, E. Evertsson, L. Thunberg, 2017, Chirality.

Selector enantioselectivity derived from chromatographic and NMR data

S. Allenmark, L. Thunberg, 2004 .

Solvent-dependent enantioselective interaction of some bis-allylamide chiral selectors studied by NMR.

U. Skogsberg, S. Allenmark, L. Thunberg, 2001, Chirality.