U
Uwe Beifuss
Researcher at University of Hohenheim
Publications - 16
Citations - 285
Uwe Beifuss is an academic researcher from University of Hohenheim. The author has contributed to research in topics: Catalysis & One-pot synthesis. The author has an hindex of 7, co-authored 16 publications receiving 253 citations. Previous affiliations of Uwe Beifuss include University of Konstanz.
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Influence of bases and ligands on the outcome of the Cu(I)-catalyzed oxidative homocoupling of terminal alkynes to 1,4-disubstituted 1,3-diynes using oxygen as an oxidant.
TL;DR: The efficient Cu(I)-catalyzed oxidative homocoupling of terminal alkynes in the presence of a base using an amine as a ligand and oxygen as an oxidant yields the symmetrical 1,3-diynes with yields of up to 99%.
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Laccase-catalyzed oxidation of Hantzsch 1,4-dihydropyridines to pyridines and a new one pot synthesis of pyridines
TL;DR: Combination of the Hantzsch 1,4-dihydropyridine synthesis with the newly developed laccase-catalyzed oxidation forms the basis of a facile and environmentally benign method for the synthesis of pyridines in one pot.
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Triethyl Phosphite Mediated Domino Reaction: Direct Conversion of ω-Nitroalkenes Into N-Heterocycles
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Reaction of 1-nitroso-2-naphthols with α-functionalized ketones and related compounds: the unexpected formation of decarbonylated 2-substituted naphtho[1,2-d][1,3]oxazoles.
TL;DR: Reactions between 1-nitroso-2-naphthols and α-functionalized ketones under basic conditions delivered 2-substituted naphtho[1,2-d][1,3]oxazoles in a single synthetic operation.
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From Nitrobenzenes to Substituted Tetrahydroquinolines in a Single Step by a Domino Reduction/Imine Formation/Aza-Diels–Alder Reaction
TL;DR: The three-component reaction between a nitrobenzene, an aldehyde, and a dienophile in the presence of iron powder as a reductant and montmorillonite K10 as a catalyst in aqueous citric acid delivers the products of an aza-Diels-Alder (Povarov) reaction with high endo-selectivity and yields up to 99%.