Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Christian Däschlein"'
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 2, Pp o383-o383 (2009)
The title compound, C19H27N2O+·Br−, is the hydrobromide of the trapping product of lithiated N,N,N′,N′-tetramethylethylenediamine (TMEDA) with benzophenone. Thereby, the N atom of the NMe2 group is selectively protonated and the respective tra
Externí odkaz:
https://doaj.org/article/0b5c30105fc24e068e9a1090c134fe4f
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 10, Pp o1950-o1950 (2008)
The title compound, C26H34NSi2+·Cl−, shows chirality at silicon. Because of its highly selective synthesis with an e.r. of >99:1 by means of a racemic resolution with mandelic acid, the free disilane is of great importance to the chemistry of high
Externí odkaz:
https://doaj.org/article/c0fdf44635e844fa871a53f2542ba04b
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 4, Pp o687-o687 (2008)
The molecule of the title compound, C8H18N2, possesses C2 symmetry. Owing to its stereochemistry, it is used in the synthesis of chiral ligands and metal complexes for asymmetric synthesis. The cyclohexane ring shows a chair conformation with the ami
Externí odkaz:
https://doaj.org/article/eb8ac83798244003aee01ec63699be22
Autor:
Matthias Breuning, Tobias Häuser, Christian Mehler, Christian Däschlein, Carsten Strohmann, Andreas Oechsner, Holger Braunschweig
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 5, Iss 1, p 81 (2009)
An enantioselective route to four tricyclic amino acids and N-tosylamides, composed of a central norbornane framework with a 2-endo,3-endo-annelated pyrrolidine ring and a 5-endo-C1 or -C2 side chain, has been developed. A key intermediate was the ch
Externí odkaz:
https://doaj.org/article/7439a4e28c684dd58105c8493d56af6c
Autor:
Lukas Fischer, Sven Sören Hartmann, Artjom Maljusch, Christian Däschlein, Oleg Prymak, Mathias Ulbricht
Publikováno v:
Journal of Membrane Science. 669:121306
We fabricated dense anion-exchange membranes from the same polymer with variations in the self-assembled hydrophilic and hydrophobic domains. We show how the nanostructure forms during membrane formation and how it can be tuned by rationally designin
Publikováno v:
European Journal of Inorganic Chemistry. 2011:1454-1465
The reactivity of enantiomerically pure lithiosilanes against aliphatic and aromatic halo electrophiles has been investigated with the focus on product composition and enantiomeric ratios as a basis for a better understanding of ongoing mechanisms. B
Publikováno v:
Chemistry - A European Journal. 15:3320-3334
Organolithium chemistry! An overview of the structure formation principles and the strong structure–reactivity relationship of lithium organics is given. By means of the commonly used lithium bases the deaggregation of the oligomeric parent structu
Autor:
Carsten Strohmann, Christian Däschlein
Publikováno v:
European Journal of Inorganic Chemistry. 2009:43-52
A series of (–)-sparteine-coordinated lithiosilanes was synthesised and studied by X-ray structural analysis. All lithiosilanes are monomers in the solid state; yet, increasing sizes of substituents at silicon significantly influences their molecul
Autor:
Carsten Strohmann, Christian Däschlein
Publikováno v:
Organometallics. 27:2499-2504
(R)-PhMe(CH2NC5H10)SiGeMe3, the first enantiomerically pure silagermane with stereoinformation at the silicon, was synthesized via a lithiosilane with retention of configuration. Further reaction w...
Publikováno v:
Angewandte Chemie. 119:4864-4866