Zobrazeno 1 - 10
of 153
pro vyhledávání: '"Berit Olofsson"'
Publikováno v:
JACS Au, Vol 4, Iss 8, Pp 2832-2837 (2024)
Externí odkaz:
https://doaj.org/article/5102f3ca0f4b4e8da1b7fd49eddf3538
Autor:
Arman Izadi, Yasaman Karami, Eleni Bratanis, Sebastian Wrighton, Hamed Khakzad, Maria Nyblom, Berit Olofsson, Lotta Happonen, Di Tang, Martin Sundwall, Magdalena Godzwon, Yashuan Chao, Alejandro Gomez Toledo, Tobias Schmidt, Mats Ohlin, Michael Nilges, Johan Malmström, Wael Bahnan, Oonagh Shannon, Lars Malmström, Pontus Nordenfelt
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-22 (2024)
Abstract Streptococcus pyogenes can cause invasive disease with high mortality despite adequate antibiotic treatments. To address this unmet need, we have previously generated an opsonic IgG1 monoclonal antibody, Ab25, targeting the bacterial M prote
Externí odkaz:
https://doaj.org/article/be6b5c313b7e4a23b226edf27ac9fea5
Pathogen-driven degradation of endogenous and therapeutic antibodies during streptococcal infections
Autor:
Alejandro Gomez Toledo, Eleni Bratanis, Erika Velásquez, Sounak Chowdhury, Berit Olofsson, James T. Sorrentino, Christofer Karlsson, Nathan E. Lewis, Jeffrey D. Esko, Mattias Collin, Oonagh Shannon, Johan Malmström
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract Group A streptococcus (GAS) is a major bacterial pathogen responsible for both local and systemic infections in humans. The molecular mechanisms that contribute to disease heterogeneity remain poorly understood. Here we show that the transit
Externí odkaz:
https://doaj.org/article/bce37cf8902b4d488654606c706f6c47
Publikováno v:
Frontiers in Chemistry, Vol 12 (2024)
The transition-metal free S-vinylation of thiophenols by vinylbenziodoxolones (VBX) constituted an important step forward in hypervalent iodine-mediated vinylations, highlighting the difference to vinyliodonium salts and that the reaction outcome was
Externí odkaz:
https://doaj.org/article/ff491f0ed8244789bd76751b61fa5277
Autor:
Erika Linde, Berit Olofsson
Publikováno v:
STAR Protocols, Vol 3, Iss 4, Pp 101700- (2022)
Summary: N- and O-arylated compounds are prevalent in pharmaceuticals and materials, and efficient approaches for their synthesis are important. Herein, we present an efficient protocol for the diarylation of aliphatic amines and water with two struc
Externí odkaz:
https://doaj.org/article/0c66490bde304b25b41c49e5d073cee5
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1491-1497 (2018)
A transition metal-free formal synthesis of phenoxazine is presented. The key step of the sequence is a high-yielding O-arylation of a phenol with an unsymmetrical diaryliodonium salt to provide an ortho-disubstituted diaryl ether. This species was c
Externí odkaz:
https://doaj.org/article/9b47b4c09ac249ef870dd71b9ab5c945
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e90921 (2014)
A striking feature of microvascular endothelial cells is their capacity to fuse and differentiate into tubular structures when grown in three-dimensional (3D) extracellular matrices, in collagen or Matrigel, mimicking the in vivo blood vessel formati
Externí odkaz:
https://doaj.org/article/5f7d197533bb400b8e570fbe4c51a468
Autor:
Bo G Lindberg, Eleanor A Merritt, Melanie Rayl, Chenxiao Liu, Ingela Parmryd, Berit Olofsson, Ingrid Faye
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e73868 (2013)
Despite efficient vector transmission, Plasmodium parasites suffer great bottlenecks during their developmental stages within Anopheles mosquitoes. The outcome depends on a complex three-way interaction between host, parasite and gut bacteria. Althou
Externí odkaz:
https://doaj.org/article/eb63dc2a416d42eeae78f0305fb3c9e4
Publikováno v:
Chemical Communications. 59:5047-5050
A metal-free synthetic route to ortho-functionalized azobenzenes via novel diaryliodonium salts, which are used to efficiently arylate nucleophiles.
Synthesis of Highly Functionalized Diarylamines through an N-, C-Cascade Reaction via Ammonium Salts
Autor:
Erika Linde, Berit Olofsson
The diarylation and skeletal diversification of unstrained cyclic amines was exploited to expand and modify the favorable properties of this important substrate class with pivotal roles in drug discovery. Cyclic amines were employed in the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0177b37b6eca2251d9ad28ee8cd82578
https://doi.org/10.26434/chemrxiv-2023-5pzhz
https://doi.org/10.26434/chemrxiv-2023-5pzhz