Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jannie Christensen"'
Autor:
Jannie Christensen, Marianne Glasius, Annie Aarup Jensen, Peter Møller, Jakob Hjort Bønløkke, Torben Sigsgaard, Dorina Gabriela Karottki, Steffen Loft
Publikováno v:
Environmental and Molecular Mutagenesis. 55:652-661
Exposure to particles from combustion of wood is associated with respiratory symptoms, whereas there is limited knowledge about systemic effects. We investigated effects on systemic inflammation, oxidative stress and DNA damage in humans who lived in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5127749e23019c4ee0c806379bc85e57
https://doi.org/10.1002/em.21877
https://doi.org/10.1002/em.21877
Publikováno v:
Christensen, J, Albrecht, L & Jørgensen, K A 2013, ' Stereocontrolled Organocatalytic Strategy for the Synthesis of Optically Active 2,3-Disubstituted cis-2,3-Dihydrobenzofurans ', Chemistry-An Asian Journal, vol. 8, no. 3, pp. 648-652 . https://doi.org/10.1002/asia.201201072
An intramolecular, organocatalyzed Michael addition has been developed to obtain biologically important 2,3-disubstituted cis-2,3-dihydrobenzofurans. By using mandelic acid salts of primary aminocatalysts, derived from cinchona alkaloids, the intramo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b0aaf0d5a0490482a38db682bb61960
https://doi.org/10.1002/asia.201201072
https://doi.org/10.1002/asia.201201072
Publikováno v:
ChemInform. 44
The biologically important title compounds are synthesized by an intramolecular, organocatalyzed Michael addition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ade68d27aa317ef8c30615aacb44eb06
https://doi.org/10.1002/chin.201329103
https://doi.org/10.1002/chin.201329103
Autor:
Alberto Fraile, Fabio Cruz Acosta, Jannie Christensen, Anna Albrecht, Karl Anker Joergensen, Lukasz Albrecht
Publikováno v:
ChemInform. 44
Diversely functionalized tetrahydroxanthones are prepared from 2,4-dienals and activated 3-cyanochromones via a [4+2] cycloaddition reaction catalyzed by squaramide-based catalyst SQA.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::643cfb79f30b81a1d93bc1bafb1dda08
https://doi.org/10.1002/chin.201306098
https://doi.org/10.1002/chin.201306098
Enantioselective H-Bond-Directing Approach for Trienamine-mediated Reactions in Asymmetric Synthesis
Autor:
Łukasz Albrecht, Karl Anker Jørgensen, Jannie Christensen, Alberto Fraile, Fabio Cruz Acosta, Anna Albrecht
Publikováno v:
Albrecht, L K, Cruz Acosta, F, Fraile Carrasco, A, Albrecht, A, Christensen, J & Jørgensen, K A 2012, ' Enantioselective H-Bond-Directing Approach for Trienamine-mediated Reactions in Asymmetric Synthesis ', Angewandte Chemie International Edition, vol. 51, no. 36, pp. 9088–9092 . https://doi.org/10.1002/anie.201204790
Right direction: The presented enantioselective strategy for the preparation of diversely functionalized tetrahydroxanthones is based on a trienamine-mediated cycloaddition between 2,4-dieneals and activated chromones. It is possibile to control the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3590c382eff003667d1aeab3cca77a70
https://pure.au.dk/portal/da/publications/enantioselective-hbonddirecting-approach-for-trienaminemediated-reactions-in-asymmetric-synthesis(cc2bb177-1723-4030-9dda-f8210b4f9768).html
https://pure.au.dk/portal/da/publications/enantioselective-hbonddirecting-approach-for-trienaminemediated-reactions-in-asymmetric-synthesis(cc2bb177-1723-4030-9dda-f8210b4f9768).html
