Rueping, Magnus.
Magnus Rueping researcher
VIAF ID: 329145857889523020569 (Personal)
Permalink: http://viaf.org/viaf/329145857889523020569
Preferred Forms
- 100 0 _ ‡a Magnus Rueping ‡c researcher
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- 100 1 _ ‡a Rueping, Magnus
- 100 1 _ ‡a Rueping, Magnus
- 100 1 _ ‡a Rueping, Magnus
- 100 1 _ ‡a Rueping, Magnus
- 100 1 _ ‡a Rueping, Magnus
-
4xx's: Alternate Name Forms (2)
5xx's: Related Names (5)
- 551 _ _ ‡a Aachen ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
- 510 2 _ ‡a ETH, Eidgenössische Technische Hochschule
- 510 2 _ ‡a Eidgenössische Technische Hochschule Zürich ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 510 2 _ ‡a RWTH Aachen ‡b Institut für Organische Chemie ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 510 2 _ ‡a RWTH Aachen ‡b Institut für Organische Chemie
Works
Title | Sources |
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Asymmetric Brønsted Acid Catalysis | |
Brønsted Base Assisted Photoredox Catalysis Proton Coupled Electron Transfer for Remote C−C Bond Formation via Amidyl Radicals | |
Cascade Cross-Coupling of Dienes Photoredox and Nickel Dual Catalysis | |
Dehydrogenative Aromatization and Sulfonylation of Pyrrolidines Orthogonal Reactivity in Photoredox Catalysis | |
Development of new synthetic methods for trifuormethylchalcogenation and fluorination of organic molecules | |
Hydride Transfer Enables the Nickel‐Catalyzed ipso ‐Borylation and Silylation of Aldehydes | |
Molecular Dynamics Simulations of Small Peptides : Can One Derive Conformational Preferences from ROESY Spectra? | |
Nickel catalyzed multicomponent stereodivergent synthesis of olefins enabled by electrochemistry, photocatalysis and photo-electrochemistry | |
One Amine-3 Tasks: Reductive Coupling of Imines with Olefins in Batch and Flow | |
Oxidative Addition to Palladium(0) Made Easy through Photoexcited-State Metal Catalysis: Experiment and Computation | |
Tuning Optical Properties of BODIPY Dyes by Pyrrole Conjugation for Photoacoustic Imaging | |
An Unexpected Boron Rearrangement Leads to a Fluorogenic and Colorimetric BODIPY Probe |