Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Emma Bratt"'
Autor:
Ira G. Schulman, Daniel Hovdal, Emma Evertsson, Emma Bratt, Anna Y. Belorusova, Eva-Lotte Lindstedt, Peter Åkerblad, Jenny Sandmark, Ingela Maxvall
Publikováno v:
Communications Biology, Vol 2, Iss 1, Pp 1-13 (2019)
Communications Biology
'Communications Biology ', vol: 2, pages: 431-1-431-13 (2019)
Communications Biology
'Communications Biology ', vol: 2, pages: 431-1-431-13 (2019)
Liver X receptors (LXRs) are attractive drug targets for cardiovascular disease treatment due to their role in regulating cholesterol homeostasis and immunity. The anti-atherogenic properties of LXRs have prompted development of synthetic ligands, bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fefa10f2b5d5c6ae47b7a89b555f36c5
http://link.springer.com/article/10.1038/s42003-019-0675-0
http://link.springer.com/article/10.1038/s42003-019-0675-0
Autor:
Nils Pemberton, Henrik Gradén, Per H. Svensson, Emma Evertsson, Petra Johannesson, Matti Lepistö, Emma Bratt
Publikováno v:
ACS Medicinal Chemistry Letters. 3:574-578
An efficient synthesis of aryl substituted cyclic sulfonimidamides designed as chiral nonplanar heterocyclic carboxylic acid bioisosteres is described. The cyclic sulfonimidamide ring system could be prepared in two steps from a trifluoroacetyl prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f46e16a225002fdb63d341f3505dd0de
https://doi.org/10.1021/ml3000935
https://doi.org/10.1021/ml3000935
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e796fb4b8c01a2f6111b9568e0de9c4
https://doi.org/10.1002/chin.201438096
https://doi.org/10.1002/chin.201438096
Suzuki-Miyaura cross-coupling reactions of heteroaromatics catalyzed by palladium supported in the cavities of amino-functionalized siliceous mesocellular foam are presented. The nanopalladium catalyst effectively couples not only heteroaryl halides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae59428eb5645f255f48047aef992a14
http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-104396
http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-104396
Publikováno v:
Chemical Communications
The oxidative rearrangement of 1,3-diketones is an underexplored alternative to enolate chemistry in the synthesis of all-carbon quaternary carboxylates. The mechanistic investigation of this reaction has resulted in a mild base mediated protocol, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6061349d9fd9b13205c88b8c534460be