T
Toan Dao-Huy
Researcher at Vienna University of Technology
Publications - 6
Citations - 1105
Toan Dao-Huy is an academic researcher from Vienna University of Technology. The author has contributed to research in topics: Furan & Regioselectivity. The author has an hindex of 2, co-authored 6 publications receiving 773 citations.
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Journal ArticleDOI
A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistry.
Carlo Sambiagio,David Schönbauer,Remi Blieck,Toan Dao-Huy,Gerit Pototschnig,Patricia Schaaf,Thomas Wiesinger,Muhammad Farooq Zia,Joanna Wencel-Delord,Tatiana Besset,Bert U. W. Maes,Michael Schnürch +11 more
TL;DR: The present review is devoted to summarizing the recent advances (2015–2017) in the field of metal-catalysed group-directed C–H functionalisation.
Journal ArticleDOI
Direct Arylation of Benzo[b]furan and Other Benzo-Fused Heterocycles.
TL;DR: This is the first systematic study of the direct arylation of benzo[b]furan with a range of functional groups tolerated, providing quick access to a variety of arylated benzo-fused heterocycles that would be accessible more elaborately using classical synthetic strategies.
Journal ArticleDOI
Synthesis of endo- and exo-N-Protected 5-Arylated 2-Aminothiazoles through Direct Arylation: An Efficient Route to Cell Differentiation Accelerators
Toan Dao-Huy,Birgit J. Waldner,Birgit J. Waldner,Laurin Wimmer,Michael Schnürch,Marko D. Mihovilovic +5 more
TL;DR: The improved direct arylation protocol was applied to structurally isomeric and nonaromatic 3-benzyl-N-phenylthiazol-2(3H)-imine and exclusive regioselectivity in the 5-position could be achieved.
Journal ArticleDOI
Structural Features Defining NF-κB Inhibition by Lignan-Inspired Benzofurans and Benzothiophenes.
Toan Dao-Huy,Simone Latkolik,Julia Bräuer,Andreas Pfeil,Hermann Stuppner,Michael Schnürch,Verena M. Dirsch,Marko D. Mihovilovic +7 more
TL;DR: It was found that both the side chain in position five and the substitution pattern of the aryl moiety in position two have a significant influence on the inhibitory activity of NF-κB.