C
Constantin G. Daniliuc
Researcher at University of Münster
Publications - 677
Citations - 16344
Constantin G. Daniliuc is an academic researcher from University of Münster. The author has contributed to research in topics: Borane & Frustrated Lewis pair. The author has an hindex of 56, co-authored 608 publications receiving 12419 citations. Previous affiliations of Constantin G. Daniliuc include Nagoya University & Braunschweig University of Technology.
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6-Trifluoromethyl-Phenanthridines through Radical Trifluoromethylation of Isonitriles
TL;DR: Development of new methods for C CF3 bond formation has caught great attention from the synthetic community during the past few years and different methods for the trifluoromethylation of arenes have been developed.
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General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands.
Zhi-Jun Jia,Zhi-Jun Jia,Christian Merten,Rajesh Gontla,Constantin G. Daniliuc,Andrey P. Antonchick,Andrey P. Antonchick,Herbert Waldmann,Herbert Waldmann +8 more
TL;DR: The three-step gram-scale synthesis of a structurally diverse and widely applicable chiral Cp ligand collection (JasCp ligands) with highly variable and adjustable structures is described.
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6-Phosphorylated Phenanthridines from 2-Isocyanobiphenyls via Radical C–P and C–C Bond Formation
TL;DR: A C-P bond and a C-C bond are formed in the synthesis of 6-phosphorylated phenanthridines starting with readily prepared 2-isocyanobiphenyls and commercially available P-radical precursors.
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Cooperative N-Heterocyclic Carbene/Palladium-Catalyzed Enantioselective Umpolung Annulations
TL;DR: The development of such a cooperative catalytic system dramatically expands the scope of NHC organocatalysis by opening up new metal-catalyzed reaction pathways for homoenolate intermediates.
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N-Aminopyridinium Salts as Precursors for N-Centered Radicals – Direct Amidation of Arenes and Heteroarenes
TL;DR: It is shown that direct radical C-H amination of heteroarenes and arenes can be achieved with N-aminopyridinium salts under mild conditions by using photoredox catalysis.