Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Arne Soicke"'
Autor:
Jiang Ren, Judith Bruns, Peter Lindemann, Kathrin Motzny, Ronald Kühne, Slim Chiha, Matthias M. Müller, Monika Beerbaum, Robert Opitz, Stephan Dohmen, Matthias Barone, Arne Soicke, Marco Tobias Klein, Dominik Albat, Peter Schmieder, Udo Heinemann, Hartmut Oschkinat, Yvette Roske, Marc Nazaré, Hans-Günther Schmalz, Peter ten Dijke, Rudolf Volkmer, Maarten van Dinther
Publikováno v:
Proceedings of the National Academy of Sciences, 117(47), 29684-29690. NATL ACAD SCIENCES
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America
Significance Protein–protein interactions mediated by proline-rich motifs are involved in regulation of many important signaling cascades. These motifs belong to the most abundant recognition motifs in the eukaryotic genome and preferentially adopt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f3f020fdbbb67aa9a4b024f1290a866
https://hdl.handle.net/1887/3185199
https://hdl.handle.net/1887/3185199
Autor:
Robert Opitz, Arne Soicke, Matthias Müller, Judith Bruns, Matthias Barone, Ronald Kühne, Jörg-Martin Neudörfl, Hans-Günther Schmalz, Slim Chiha
Publikováno v:
European Journal of Organic Chemistry. 2018:455-460
Autor:
Marco Tobias Klein, Slim Chiha, Robert Opitz, Arne Soicke, Matthias Barone, Hans-Günther Schmalz, Jörg-Martin Neudörfl, Cédric Reuter, Ronald Kühne, Stephan Dohmen
Publikováno v:
Chemistry - A European Journal. 21:8464-8470
With the aim of developing polyproline type II helix (PPII) secondary-structure mimetics for the modulation of prolin-rich-mediated protein-protein interactions, the novel diproline mimetic ProM-2 was designed by bridging the two pyrrolidine rings of
Autor:
Arne Soicke, Nils Schlörer, Matthias Winter, Ronald Kühne, Jörg-Martin Neudörfl, Cédric Reuter, Hans-Günther Schmalz
Publikováno v:
European Journal of Organic Chemistry. 2014:6467-6480
Polycyclic proline-derived scaffolds (ProMs) have recently demonstrated their value as conformationally defined dipeptide analogs for the modular construction of secondary structure mimetics, specifically interfering with PPII helix-mediated protein
Publikováno v:
Synlett. 2011:2487-2490
On treatment with boron trifluoride etherate as a Lewis acid, acetophenone and benzophenone derivatives bearing a prenyl (or a related) side chain in ortho-position were shown to undergo intramolecular carbonyl―olefin metathesis, in the absence of
Publikováno v:
Journal of the American Chemical Society. 133:6948-6951
A one-pot protocol for the cyanomethylation of aryl halides through a palladium-catalyzed reaction with isoxazole-4-boronic acid pinacol ester was developed. Mechanistically, the reaction proceeds through (1) Suzuki coupling, (2) base-induced fragmen
Autor:
Ronald Kuehne, Joerg‐Martin Neudoerfl, Hans‐Guenther Schmalz, Arne Soicke, Matthias Winter, Nils Schloerer, Cédric Reuter
Publikováno v:
ChemInform. 46
Synthons (VI) and (Xb) are prepared and used in the peptide coupling with proline derivative (XI).
Autor:
Christian Freund, Robert Opitz, Peter Schmieder, Ronald Kühne, Burkhard Wiesner, Cédric Reuter, Monika Beerbaum, Peter H. Huy, Matthias Müller, Kirill Piotukh, Matthias Barone, Yvette Roske, Michael Beyermann, Hans-Günther Schmalz, Arne Soicke, Hartmut Oschkinat, Rudolf Volkmer
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 112(16): 5011–5016
Small-molecule competitors of protein–protein interactions are urgently needed for functional analysis of large-scale genomics and proteomics data. Particularly abundant, yet so far undruggable, targets include domains specialized in recognizing pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0afb73efb3c416b04cc38d1fd4f4c532
https://repository.publisso.de/resource/frl:6405497
https://repository.publisso.de/resource/frl:6405497
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[928664-98-6] C9H14BNO3 (MW: 195.11) InChI = 1S/C9H14BNO3/c1-8(2)9(3,4)14-10(13-8)7-5-11-12-6-7/h5-6H,1-4H3 InChIKey = LXCICYRNWIGDQA-UHFFFAOYSA-N (Suzuki coupling reagent, acetonitrile anion equivalent1, 2) Physical Data: mp 109–112 °C. Solubilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9185f289ee46abf12782ec99391a78f4
https://doi.org/10.1002/047084289x.rn01478
https://doi.org/10.1002/047084289x.rn01478
Publikováno v:
ChemInform. 43
Attempted selective demethylation of substrate (Ia) during the synthesis of pestalone affords instead a cyclized product (IIa).