Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Hans Emtenäs"'
Autor:
Andrew D. Campbell, Staffan Karlsson, Štefan Moravčík, Hanna Leek, Kuangchu Dai, Matthew R. Tatton, Kristina Öhlén, Hucheng Zhao, Marcus Malmgren, Hans Emtenäs, Anna-Carin C. Carlsson, Grigorios Nikitidis, Calum Cook, Anna C. Jonson, Subhash Pithani
Publikováno v:
Organic Process Research & Development. 26:710-729
Autor:
Staffan Karlsson, Helen Benson, Calum Cook, Gordon Currie, Jerome Dubiez, Hans Emtenäs, Janet Hawkins, Rebecca Meadows, Peter D. Smith, Jeffrey Varnes
Publikováno v:
Organic Process Research & Development. 26:601-615
Publikováno v:
Organic Process Research & Development. 23:1926-1931
The practically and financially viable use of immobilized enzymes in the production of pharmaceutical and bulk chemicals requires highly catalytically active enzymes and efficient mass transfer of ...
Autor:
Hans Ericsson, Igor L. Shamovsky, Carl Whatling, Malin Lemurell, Marianne Swanson, Eva-Lotte Lindstedt, Johan Broddefalk, Mats Någård, Anita Dellsén, Johan Ulander, Carl Amilon, Kenneth Granberg, Annika Westin Eriksson, Daniel Pettersen, Alleyn T. Plowright, Monica Sundqvist, Hans Emtenäs, Martin A. Hayes
Publikováno v:
Journal of Medicinal Chemistry. 62:4312-4324
5-Lipoxygenase activating protein (FLAP) inhibitors attenuate 5-lipoxygenase pathway activity and reduce the production of proinflammatory and vasoactive leukotrienes. As such, they are hypothesized to have therapeutic benefit for the treatment of di
Autor:
Peter R. Moore, Hans Emtenäs, Andrew Stark, Johan Broddefalk, Staffan Karlsson, Rolf Bergman, Christian Löfberg
Publikováno v:
Organic Process Research & Development. 22:618-624
A large-scale, robust telescoped process involving acid chloride generation and Friedel–Crafts acylation followed by hydrolysis of an ester was developed for the manufacture of a homochiral disubstituted cyclohexane. Chromatography was avoided, and
Autor:
Hans Emtenäs, Paul M. Gillespie, Staffan Karlsson, Mubina Mohamed, Calum Cook, Kenny J. H. Fan
Publikováno v:
Organic Process Research & Development. 21:1668-1674
Starting from sodium azide, methyl-bromoacetate, and 3-methylbut-1-yne, a safe and efficient three-step continuous process was developed to obtain 2-(4-isopropyl-1H-1,2,3-triazol-1-yl)acetic acid. Isolation of hazardous intermediates was avoided, and
Autor:
Christian Löfberg, Marianne Swanson, ZhongQing Yuan, Johan Broddefalk, Annika Westin Eriksson, Susanne Winiwarter, Martin A. Hayes, Gabrielle Saarinen, Johan Meuller, Carl Whatling, Johan Ulander, Hans Emtenäs, Johan Cassel, Monica Sundqvist, Malin Lemurell, Luna Prieto Garcia, Staffan Karlsson
Publikováno v:
Journal of medicinal chemistry. 62(9)
5-Lipoxygenase (5-LO)-activating protein (FLAP) inhibitors have proven to attenuate 5-LO pathway activity and leukotriene production in human clinical trials. However, previous clinical candidates have been discontinued and the link between FLAP inhi
Publikováno v:
Organometallics. 27:2490-2498
The mechanism of the copper-free Sonogashira cross-coupling was investigated using a model reaction with differently para-substituted phenylacetylenes and 4-iodobenzotrifluoride as coupling partners and a Pd2(dba)3·CHCl3−AsPh3 catalyst system in m
Autor:
Susanne Winiwarter, Öjvind Davidsson, Alleyn T. Plowright, Anna Pettersen, Carl Whatling, Marie Rydén-Landergren, Johan Broddefalk, Margareta Herslöf, Jonas Gunnar Barlind, Daniel Hovdal, Kalle Sigfridsson, Tomas Drmota, Marianne Swanson, Hans Emtenäs, Antonio Llinas, Sara Moses, Johan Ulander, Anders Dahlén, Malin Lemurell
Publikováno v:
Journal of medicinal chemistry. 58(2)
A drug discovery program in search of novel 5-lipoxygenase activating protein (FLAP) inhibitors focused on driving a reduction in lipophilicity with maintained or increased ligand lipophilic efficiency (LLE) compared to previously reported compounds
Publikováno v:
Organic & Biomolecular Chemistry. 1:1308-1314
Optically active bicyclic β-lactams were synthesized, starting from 2-H-Δ2-thiazolines and Meldrum's acid derivatives. Several methods to accomplish an ester hydrolysis without damaging the β-lactam framework were investigated. A rapid CsOH saponi