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Nina Kann
Researcher at Chalmers University of Technology
Publications - 84
Citations - 1878
Nina Kann is an academic researcher from Chalmers University of Technology. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 22, co-authored 84 publications receiving 1686 citations. Previous affiliations of Nina Kann include Joseph Fourier University & Royal Institute of Technology.
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Ruthenium-Catalyzed Azide Alkyne Cycloaddition Reaction: Scope, Mechanism, and Applications.
TL;DR: The ruthenium-catalyzed azide alkyne cycloaddition affords 1,5-disubstituted 1,2,3-triazoles in one step and complements the more established copper-Catalyzed reaction providing the 1,4-isomer.
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Transition‐Metal‐Catalyzed Propargylic Substitution
Natalie Ljungdahl,Nina Kann +1 more
TL;DR: Catalytic propargylic substitution has now emerged as an efficient transformation that can be catalyzed by a variety of transition metals (see picture).
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Targeting membrane-bound viral RNA synthesis reveals potent inhibition of diverse coronaviruses including the middle East respiratory syndrome virus.
Anna Lundin,Ronald Dijkman,Tomas Bergström,Nina Kann,Beata Adamiak,Charles Hannoun,Eveline Kindler,Hulda R. Jonsdottir,Doreen Muth,Joeri Kint,Maria Forlenza,Marcel A. Müller,Christian Drosten,Volker Thiel,Edward Trybala +14 more
TL;DR: An evolutionary conserved step in the life cycle of positive-stranded RNA viruses, the recruitment of cellular membranes for viral replication, as vulnerable and, most importantly, druggable target for antiviral intervention is proposed.
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Sequential One-Pot Ruthenium-Catalyzed Azide-Alkyne Cycloaddition from Primary Alkyl Halides and Sodium Azide
TL;DR: An experimentally simple sequential one-pot RuAAC reaction, affording 1,5-disubstituted 1H-1,2,3-triazoles in good to excellent yields starting from anAlkyl halide, sodium azide, and an alkyne, is reported.
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An iron carbonyl approach to the influenza neuraminidase inhibitor oseltamivir
TL;DR: A novel synthetic route towards oseltamivir, an influenza neuraminidase inhibitor, has been achieved employing a cationic iron carbonyl complex, providing an alternate pathway with the potential to access diverse analogues.