Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Benjamin Heinz"'
Autor:
Fiona Siemens, Benjamin Martin, Dimitrije Djukanovic, Paul Knochel, Benjamin Heinz, Mohamed Idriess
Publikováno v:
Synthesis. 54:5055-5063
The treatment of 3-halopyridines (Cl, Br) bearing an R-substituent in position 2 (R = OEt, NEt2, N-piperidyl, or SEt) or in position 5 (R = OMe, OEt, SEt, NMe2, NEt2, or aryl) with KHMDS and an amine at 25 °C for 12 hours in THF provided regioselect
Autor:
Benjamin Heinz, Benjamin Martin, Johannes H. Harenberg, Rajasekar Reddy Annapureddy, Dimitrije Djukanovic, Paul Knochel, Niels Weidmann
Publikováno v:
Reference Module in Chemistry, Molecular Sciences and Chemical Engineering
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::794acf4674a61e973d774f5481988e46
https://doi.org/10.1016/b978-0-12-820206-7.00040-8
https://doi.org/10.1016/b978-0-12-820206-7.00040-8
Publikováno v:
Chemistry – A European Journal. 28
Mixed TMP-bases (TMP=2,2,6,6-tetramethylpiperidyl), such as TMPMgCl ⋅ LiCl, TMP2 Mg ⋅ 2LiCl, TMPZnCl ⋅ LiCl and TMP2 Zn ⋅ 2LiCl, are outstanding reagents for the metalation of functionalized aromatics and heterocycles. In the presence of Lewi
Autor:
Francesca Mandrelli, Paolo Filipponi, Benjamin Martin, Serena Mostarda, Benjamin Heinz, Paul Knochel, Dimitrije Djukanovic
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
The continuous flow reaction of various aryl or heteroaryl bromides in toluene in the presence of THF (1.0 equiv) with sec‐BuLi (1.1 equiv) provided at 25 °C within 40 sec the corresponding aryllithiums which were acylated with various functionali
Publikováno v:
Synthesis. 51:4452-4462
The thiolation of pyridine-2-sulfonamides using magnesium thiolates is reported. The ortho-functionalizations of these sulfonamides using TMPMgCl·LiCl (TMP = 2,2,6,6-tetramethylpiperidyl) followed by electrophilic quenching produced a range of 3-fun
Autor:
Moritz Balkenhohl, Konstantin Karaghiosoff, Robert Greiner, Benjamin Heinz, Ilya S. Makarov, Paul Knochel, Hendrik Zipse
Publikováno v:
Chemistry - A European Journal. 23:13046-13050
A set of successive regioselective metalations and functionalizations of the 1,5-naphthyridine scaffold are described. A combination of Zn-, Mg-, and Li-TMP (TMP = 2,2,6,6-tetramethylpiperidyl) bases and the presence or absence of a Lewis acid (BF3 c
Autor:
Johannes H. Harenberg, Maximilian A. Ganiek, Niels Weidmann, Paul Knochel, Alexandre Desaintjean, Benjamin Heinz
Publikováno v:
Opérations unitaires. Génie de la réaction chimique.
Cet article decrit la preparation d’especes organometalliques du magnesium et du zinc et leur emploi en flux continu. Par des reactions de metallations de systemes aromatiques et heterocycliques, il est possible de preparer des magnesiens et zinciq
Publikováno v:
Organic letters. 20(24)
The amination of various phosphorodiamidate-substituted pyridines, quinolines, and quinoxaline with magnesium amides R2NMgCl center dot LiCl proceeds at room temperature within 8 h. Several pharmaceutically active amines were suitable substrates for
This paper presents VideoMR: a novel map and reduce framework for real-time video processing on graphic processing units (GPUs). Using the advantages of implicit parallelism and bounded memory allocation, our approach enables developers to focus on i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6266362d561207d100a094287f2b8300
Autor:
Stefan Rüegger, Armin Hoffmann, Jan Kubelka, Benjamin Heinz, Daniel Nettels, Klaus Gast, Benjamin Schuler, Sonja Müller-Späth, Luc Reymond, Robert B. Best, Frank Küster, Domminik Haenni, Hagen Hofmann
Publikováno v:
Proceedings of the National Academy of Sciences
We used single-molecule FRET in combination with other biophysical methods and molecular simulations to investigate the effect of temperature on the dimensions of unfolded proteins. With single-molecule FRET, this question can be addressed even under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5d39fa70aba7bfd4d5af616196cd678
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/32396
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/32396