E
Elias Pershagen
Researcher at Stockholm University
Publications - 10
Citations - 566
Elias Pershagen is an academic researcher from Stockholm University. The author has contributed to research in topics: Allylic rearrangement & Cell. The author has an hindex of 7, co-authored 10 publications receiving 513 citations. Previous affiliations of Elias Pershagen include Uppsala University.
Papers
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Journal ArticleDOI
SiR-Hoechst is a far-red DNA stain for live-cell nanoscopy
Gražvydas Lukinavičius,Claudia Blaukopf,Elias Pershagen,Alberto Schena,Luc Reymond,Emmanuel Derivery,Marcos González-Gaitán,Elisa D’Este,Stefan W. Hell,Daniel W. Gerlich,Kai Johnsson +10 more
TL;DR: A far-red DNA stain, SiR–Hoechst, which displays minimal toxicity, is applicable in different cell types and tissues, and is compatible with super-resolution microscopy, which makes this probe a powerful tool for live-cell imaging.
Journal ArticleDOI
Luminescent lanthanide complexes with analyte-triggered antenna formation.
TL;DR: A new strategy for accessing analyte-responsive luminescent probes is presented, which affords nanomolar to micromolar detection limits, provides the capability to detect two analytes in parallel, and can be utilized to monitor enzymatic activity in live cells.
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Designing reactivity-based responsive lanthanide probes for multicolor detection in biological systems
Elias Pershagen,K. Eszter Borbas +1 more
TL;DR: A survey of strategies for the design and synthesis of responsive luminescent probes based on lanthanide complexes can be found in this paper, with an emphasis on the strategies that could be generalized to the detection of additional analytes.
Journal ArticleDOI
Multiplex Detection of Enzymatic Activity with Responsive Lanthanide‐Based Luminescent Probes
Elias Pershagen,K. Eszter Borbas +1 more
TL;DR: The high modularity of the probe design enabled the rapid assembly of both green and red emitters for a large variety of analytes by the simple exchange of the lanthanide or an analyte-cleavable caging group, respectively.
Journal ArticleDOI
Stereoselective Intermolecular Allylic C–H Trifluoroacetoxylation of Functionalized Alkenes
TL;DR: Pd-catalyzed allylic C-H trifluoroacetoxylation of substituted alkenes was performed using PhI(OCOCF(3))(2) as the oxidant and acyloxy source and studies with one of the possible (η(3)-allyl)Pd(II) intermediates suggest that the reaction proceeds via stereoselective formation of Pd(IV) intermediate.