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Disambiguation of "Beifuss, Uwe"

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From Nitrobenzenes to Substituted Tetrahydroquinolines in a Single Step by a Domino Reduction/Imine Formation/Aza-Diels-Alder Reaction

, , , and . Journal of organic chemistry, 80 (4): 2319-2332 (2015)
DOI: 10.1021/jo502882y

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Dr. Uwe Gaisbauer University of Stuttgart

Hon. -Prof. Dr. Uwe Pfenning University of Stuttgart

Prof. Uni. Reg. de Blumenau Uwe Menzel University of Stuttgart

Dr. rer. nat. Uwe Breitenbücher University of Stuttgart

Uwe Fischer University of Stuttgart

 

Other publications of authors with the same name

Formation of substituted 1-naphthols and related products via dimerization of alkyl 3-(o-halo(het)aryl)-oxopropanoates based on a Cul-catalyzed domino C-arylation/condensation/aromatization process, , , , , and . Tetrahedron, 72 (24): 3454-3467 (2016)Flexible Approach for the Synthesis of Annulated 4H-Pyrans Based on a Cu(I)-Catalyzed C-Allylation/O-Vinylation Reaction of Cyclic 1-Bromoallyl Tosylates with Cyclic and Acyclic 1,3-Dicarbonyls, , , and . The journal of organic chemistry, 87 (13): 8316-8341 (2022)From Nitrobenzenes to Substituted Tetrahydroquinolines in a Single Step by a Domino Reduction/Imine Formation/Aza-Diels-Alder Reaction, , , and . Journal of organic chemistry, 80 (4): 2319-2332 (2015)A novel copper-catalyzed, hydrazine-free synthesis of N-1 unsubstituted 1H-indazoles using stable guanylhydrazone salts as substrates, , , , , , , , and . Tetrahedron, (2021)Transition metal-free diastereospecific synthesis of (Z)-2-arylidene-2,3-dihydrobenzob1,4dioxines by reaction of (Z)-1,2-dibromo-3-aryl-2-propenes with catechols, , , , , and . Tetrahedron, 76 (42): 131482 (2020)Selective Catalytic Oxidation of C-H Bonds with Molecular Oxygen, , , , , , , , , and 5 other author(s). ChemCatChem, 5 (1): 82--112 (2013)Selective catalytic oxidation of C-H bonds with molecular oxygen, , , , , , , , , and 5 other author(s). ChemCatChem, 5 (1): 82-112 (2013)Synthesis of fucosylated lacto-N-tetraose using whole-cell biotransformation, , , , , and . Bioorganic & medicinal chemistry, 23 (21): 6799-6806 (2015)