Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jan, Blid"'
Publikováno v:
The Journal of Organic Chemistry. 72:1294-1300
The first asymmetric [2,3]-sigmatropic rearrangement of achiral allylic amines has been realized by quaternization of the amines with an enantiomerically pure diazaborolidine and subsequent treatment with Et3N. The resultant homoallylic amines were o
Autor:
Jan Blid, Peter Somfai
Publikováno v:
Tetrahedron Letters. 44:3159-3162
An investigation of the Lewis acid mediated [2,3]-sigmatropic rearrangement of allylic ammonium ylides has been conducted by employing various bases and boron Lewis acids. Using BBr3 together with ...
Autor:
Jenny Viklund, Ylva Gravenfors, Fredrik Jeppsson, Anders E. G. Lindgren, Anh Johansson, Jonas Malmström, Jan Blid, Karin J. Sterky, Annika Kers, Rickard Forsblom, Rikard Emond, Johanna Fälting, Tobias Ginman, Fredrik Rahm, Patrik Johansson, Margareta Bergh, Fredrik Lake, Fernando Sehgelmeble
Publikováno v:
Journal of medicinal chemistry. 56(11)
By use of iterative design aided by predictive models for target affinity, brain permeability, and hERG activity, novel and diverse compounds based on cyclic amidine and guanidine cores were synthesized with the goal of finding BACE-1 inhibitors as a
Autor:
Ylva, Gravenfors, Jenny, Viklund, Jan, Blid, Tobias, Ginman, Sofia, Karlström, Jacob, Kihlström, Karin, Kolmodin, Johan, Lindström, Stefan, von Berg, Fredrik, von Kieseritzky, Krisztian, Bogar, Can, Slivo, Britt-Marie, Swahn, Lise-Lotte, Olsson, Patrik, Johansson, Susanna, Eketjäll, Johanna, Fälting, Fredrik, Jeppsson, Kia, Strömberg, Juliette, Janson, Fredrik, Rahm
Publikováno v:
Journal of medicinal chemistry. 55(21)
Amino-2H-imidazoles are described as a new class of BACE-1 inhibitors for the treatment of Alzheimer’s disease. Synthetic methods, crystal structures, and structure–activity relationships for target activity, permeability, and hERG activity are r
Autor:
Johan Bylund, Daniel Sohn, Jan Blid, Yevgeni Besidski, Ismet Dorange, Mats Svensson, Rickard Forsblom, Ylva Gravenfors, Istvan Macsari
Publikováno v:
Bioorganicmedicinal chemistry letters. 22(22)
A novel indolizine class of compounds was identified as TRPV1 antagonist from an HTS campaign. However, this indolizine class proved to be unstable and reacted readily with glutathione when exposed to light and oxygen. Reactivity was reduced by the i
Publikováno v:
ChemInform. 35
Boron trifluoride and BBr(3) mediated [2,3]-sigmatropic rearrangements of allylic alpha-amino amides have been developed affording secondary amines in good yields. (E)-Crotyl and (E)-cinnamyl alpha-amino amides 2b and 2c exhibit excellent syn-diaster
Publikováno v:
Journal of the American Chemical Society. 127:9352-9353
An asymmetric Lewis acid-mediated [2,3]-sigmatropic rearrangement of allylic amines has been developed, affording the corresponding homoallylic amines in good yield and excellent enantioselectivities. The rearrangement proceeds by complexation of the
Autor:
Jacob Kihlström, Johan Lindström, Fredrik Jeppsson, Johanna Fälting, Can Slivo, Tobias Ginman, Susanna Eketjäll, Jenny Viklund, Fredrik Rahm, Patrik Johansson, Jan Blid, Britt-Marie Swahn, Juliette Janson, Karin Kolmodin, Ylva Gravenfors, Krisztián Bogár, Stefan von Berg, Lise-Lotte Olsson, Kia Strömberg, Fredrik von Kieseritzky, Sofia Karlström
Publikováno v:
Journal of Medicinal Chemistry. 55:10316-10316
Publikováno v:
Synthetic Metals. 120:1061-1062
1,2-ethanedisulfenyl chloride 1 has been utilized as a electrophilic reagent for the preparation of dihydro-1,4-dithiino substituted aromatics. The title reagent reacts with activated aromatics to give several new heterocyclic systems in modest yield
Autor:
Stridfeldt, Elin1, Lindstedt, Erik1, Reitti, Marcus1, Blid, Jan1, Norrby, Per‐Ola2, Olofsson, Berit1 berit.olofsson@su.se
Publikováno v:
Chemistry - A European Journal. 9/21/2017, Vol. 23 Issue 53, p13249-13258. 10p.