9th Tetrahedron Symposium, Berkeley, CA, USA, 2008
High stereoselectivity in chelation-controlled intermolecular Heck reactions of cyclic enol ether with organic chlorides.
1st International Conference on Drug Discovery and Development, Dubai, UAE
4-8 Feb, 2008
Investigation of the P1’ Substituent - Synthesis and Evaluation of Inhibitors
of Malarial Aspartic Proteases.
Kristina Orrling et al.
1st International Conference on Drug Discovery and Development, Dubai, UAE
4-8 Feb, 2008
Evaluation of Various P1' Substituents in Tertiary Alcohol Containing and Elongated HIV-1 Protaease Inhibitors.
Per Öhrngren et al.
1st International Conference on Drug Discovery and Development, Dubai, UAE
4-8 Feb, 2008
Synthesis of BACE-1 Inhibitors with a Tertiary Hydroxyl Group as the Central Core.
Fredrik Wångsell et al.
[PDF]
11th Belgian Organic Synthesis Symposium, Gent, BE, 13-18 July, 2008
Novel Procedure to Form Lactams from Lactones With the Aid of Ionic Liquids and Microwave Irradiation.
Kristina Orrling et al.
XXth International Symposium on Medicinal Chemistry, Aug 31 - Sept 4, 2008, Vienna, Austria.
Novel aspartyl protease inhibitors in the quest against malaria.
Kristina Orrling et al.
XXth International Symposium on Medicinal Chemistry 2008, Vienna, Austria, August 31 - September 4, 2008
New Macrocyclic P2 Phenylglycine-based Inhibitors Targeting Hepatitis C Virus NS3 Protease
Anna Lampa et al.
[PDF]
13th Ischia Advanced School of Organic Chemistry, Ischia, Italy, 27 Sept - 2 Oct 2008
P1' Variations oh HIV-1 Protease Inhibitors with a Tertiary-Alchohol-Containing Transition-State Mimic
Per Öhrngren et al.
13th Ischia Advanced School of Organic Chemistry, Ischia, Italy, 27 Sept - 2 Oct 2008
Synthesis of Potent BACE-1 Inhibitors Incorporating a Novel Hydroxyethylene Isostere as Central Core.
Fredrik Wångsell et al.
[PDF]
CRC International Symposium, Stockholm, Sweden, 3 November 2008
HIV-1 Protease Inhibitors with a Tertiary Alcohol-Containing Transition State Mimic – Evaluation of Various P1’ Substituents.
Per Öhrngren et al.
[PDF]