Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jiirgen Liebscher"'
Autor:
Ludwig Löser, Jiirgen Liebscher, Andreas Bunge, Anna Arbuzova, Oliver Kaczmarek, Nicolai Brodersen, Andreas Herrmann, Daniel Huster
Publikováno v:
European Journal of Organic Chemistry. 2008:1917-1928
Various new nucleosides bearing one or two lipophilic groups at the 2′-position have been synthesized. The lipophilic substituents were attached to a 2′-hydroxy, 2′-amino, or 2′-thio function. These lipophilic nucleosides anchor in large unil
Autor:
Ludwig Löser, Nicolai Brodersen, Andreas Herrmann, Jun Li, Jiirgen Liebscher, Daniel Huster, Andreas Bunge, Oliver Kaczmarek
Publikováno v:
European Journal of Organic Chemistry. 2007:6060-6069
Nucleosides were synthesized bearing one or two lipophilic groups at the 5′-position. The lipophilic substituents can be fixed at a 5′-amino group or at the 5′-phosphate moiety. Selected examples of these lipophilic nucleosides are shown by sol
Autor:
Maximilian Rost, Holger A. Scheidt, Daniel Huster, Crina Cismas, Andreas Herrmann, Jiirgen Liebscher, Wolfgang Flasche
Publikováno v:
ResearcherID
For the potential application in nanobiotechnology, we have synthesized three different lipophilic nucleosides and investigated their membrane insertion and localization by solid-state NMR spectroscopy. The hydrophilic headgroups of these nucleosides
Publikováno v:
ChemInform. 35
New N-substituted 2-amino-9,9-dialkylfluorenes optionally bearing electron-withdrawing substituents such as nitro or cyano in position 7 can be synthesized starting from 2-halo-9,9-dialkylfluorenes by Pd-catalyzed substitution with amines. Chiral ami