Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Maurice Dörr"'
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
A novel approach towards the activation of different arenes and purines including caffeine and theophylline is presented. The simple, safe and scalable electrochemical synthesis of 1,1,1,3,3,3‐hexafluoroisopropanol (HFIP) aryl ethers was conducted
Autor:
Siegfried R. Waldvogel, Robert Franke, Sebastian Lips, Maurice Dörr, Carlos A. Martínez-Huitle, Dieter Schollmeyer
Publikováno v:
Chemistry – A European Journal. 25:7835-7838
We report an innovative, sustainable and straightforward protocol for the synthesis of N,N-diarylamides equipped with nonprotected hydroxyl groups by using electrosynthesis. The concept allows the application of various substrates furnishing diarylam
Autor:
Siegfried R. Waldvogel, Robert Franke, Bernardo A. Frontana-Uribe, Maurice Dörr, Dieter Schollmeyer, Sebastian Lips
Publikováno v:
Chemistry - A European Journal. 24:6057-6061
Heterobiaryls consisting of a phenol and a benzofuran motif are of significant importance for pharmaceutical applications. An attractive sustainable, metal- and reagent-free, electrosynthetic, and highly efficient method, that allows access to (2-hyd
Publikováno v:
ChemElectroChem. 8:2616-2616
Publikováno v:
ECS Meeting Abstracts. :2500-2500
Most cross-coupling reactions make use of transition metal-based catalysts and require prefunctionalization or an excess of oxidizers. This results in large quantities of partially toxic reagent waste. By anodic cross-coupling via the oxidation of ph
Autor:
Hielscher, Maximilian M.1 (AUTHOR), Dörr, Maurice1 (AUTHOR), Schneider, Johannes1 (AUTHOR), Waldvogel, Siegfried R.1,2 (AUTHOR) waldvogel@uni-mainz.de
Publikováno v:
Chemistry - An Asian Journal. Jul2023, Vol. 18 Issue 14, p1-8. 8p.
Autor:
Hielscher, Maximilian M., Schneider, Johannes, Lohmann, Alexander H. J., Waldvogel, Siegfried R.
Publikováno v:
ChemElectroChem; 9/16/2024, Vol. 11 Issue 18, p1-7, 7p
Publikováno v:
ChemElectroChem; Dec2023, Vol. 10 Issue 23, p1-6, 6p