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Tamás Beke-Somfai

Researcher at Hungarian Academy of Sciences

Publications -  64
Citations -  1192

Tamás Beke-Somfai is an academic researcher from Hungarian Academy of Sciences. The author has contributed to research in topics: Membrane & Circular dichroism. The author has an hindex of 15, co-authored 57 publications receiving 874 citations. Previous affiliations of Tamás Beke-Somfai include Chalmers University of Technology & Eötvös Loránd University.

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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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Characterization of extracellular vesicles by IR spectroscopy: Fast and simple classification based on amide and CH stretching vibrations.

TL;DR: ATR-FTIR measurements provide a simple and reproducible method for the screening of extracellular vesicle preparations and the potential applicability of this technique for fast and efficient characterization of vesicular components is high as the investigated samples require no further preparations and all the different molecular species can be determined in the same sample.
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Characterization of the thermal and photoinduced reactions of photochromic spiropyrans in aqueous solution.

TL;DR: Six water-soluble spiropyran derivatives have been characterized with respect to the thermal and photoinduced reactions over a broad pH-interval and the nonprotonated merocyanine isomer is susceptible to hydrolysis, whereas the corresponding protonated form is stable toward hydrolytic degradation.
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UV Transition Moments of Tyrosine

TL;DR: The inhomogeneous solvent-shift sensitivity in combination with robust polarization can be exploited for analyzing tyrosine orientation distributions in protein complexes using LD spectroscopy.
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Michler’s Hydrol Blue: A Sensitive Probe for Amyloid Fibril Detection

TL;DR: Michler's hydrol blue (MHB) is investigated with respect to photophysical properties in varied solvent environment and when bound to insulin and lysozyme fibrils, where it exhibits a characteristic red-shift in its excitation spectrum and an increase in the emission quantum yield upon binding.