Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Marina Schinnerl"'
Autor:
Sabine Clauss, C Ebner, Elisabeth Thell, Marina Schinnerl, Alexander Reinthaller, Birgit Hofstätter, G Bogner, Katharina Hrauda, Mirijam Hall, Andrea Schilcher, Christian F. Singer, Thomas Aigmüller, I Tsibulak, Johanna Hell-Teutsch, Daniela Gangl, K Knoll, E Reiser, Doris Hittler, Gottfried Gamperl, Barbara Puschacher, Cornelia Weirather, Johanna Pozniak, Verena Sigl, Edgar Petru, Christian Marth, K Leitner, Sebastian Alicke, Tatjana Weiss, Szabolcs Bozsa
Publikováno v:
International Journal of Gynecologic Cancer
International Journal of Gynecological Cancer
International Journal of Gynecological Cancer
BackgroundOn March 16, 2020, the federal government of Austria declared a nationwide lockdown due to the COVID-19 pandemic. Since the lockdown, screening examinations and routine checkups have been restricted to prevent the spread of the virus and to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6236843389ec8e5a1507fec14a52cc91
https://doi.org/10.1136/ijgc-2020-001975
https://doi.org/10.1136/ijgc-2020-001975
Autor:
William C. K. Pomerantz, Peter Wipf, Myung Ryul Lee, Samuel H. Gellman, Marina Schinnerl, Xiaodong Wang, Tami L. Raguse
Publikováno v:
Organic Letters. 9:1801-1804
[structure: see text] beta-Peptides containing residues derived from trans-2-aminocyclohexanecarboxylic acid (ACHC) display high population of 14-helical secondary structure in aqueous solution. We show that hydrophobic interactions between cyclohexy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5428f3a5b95d8ae6c2fa200dccfd480c
https://doi.org/10.1021/ol070511r
https://doi.org/10.1021/ol070511r
Publikováno v:
European Journal of Organic Chemistry. 2003:721-726
We report a synthesis of a protected derivative of trans-4-aminopiperidine-3-carboxylic acid (APiC). The route provides either enantiomer. All intermediates are purified by crystallization, and large-scale preparation is therefore possible. An analog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1259d8c423b7507f4e2650a1bc6ee12d
https://doi.org/10.1002/ejoc.200390112
https://doi.org/10.1002/ejoc.200390112
Autor:
Emilio Parisini, Oliver Reiser, Thomas Labahn, Marina Schinnerl, Claudius Böhm, Manfred Zabel, Christian Bubert
Publikováno v:
Scopus-Elsevier
The stereoselective synthesis of highly functionalized 1,2,3-trisubstituted cyclopropanes 1 and 2, starting from readily available furans 3 or N-protected pyrrole 4, is described. Furthermore, exceptionally high diastereocontrol in agreement with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dde6608c131d8b405c49511334e4acc3
https://doi.org/10.1002/1099-0690(200008)2000:16<2955::aid-ejoc2955>3.0.co
https://doi.org/10.1002/1099-0690(200008)2000:16<2955::aid-ejoc2955>3.0.co
Publikováno v:
ChemInform. 33
The enantioselective addition of ZnR2 to aldehydes (1,2) and cyclic enones (1,4) was accomplished using bis(oxazolines) as chiral ligands. The requirement for hydroxymethylene side chains in the ligands strongly suggests that bimetallic catalysts are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd05af08896252a2f3d4cb57205a5fb7
https://doi.org/10.1002/chin.200222034
https://doi.org/10.1002/chin.200222034
Publikováno v:
ChemInform. 34
The diastereo- and enantioselective cyclopropanation of furans was achieved in up to 91% ee using a new set of chiral bis(oxazoline) ligands that are able to use secondary binding sites to enhance selectivity. In contrast, with substrates such as sty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c19fd566a5f763f7c7d3169933ff2f86
https://doi.org/10.1002/chin.200330039
https://doi.org/10.1002/chin.200330039
Autor:
Manfred Zabel, Oliver Reiser, Emilio Parisini, Marina Schinnerl, Christian Bubert, Thomas Labahn, Claudius Boehm
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9adad53a9379289cadc783289f6b098f
https://doi.org/10.1002/chin.200104096
https://doi.org/10.1002/chin.200104096
Publikováno v:
Organic Letters. 4:471-471
The enantioselective addition of ZnR(2) to aldehydes (1,2) and cyclic enones (1,4) was accomplished using bis(oxazolines) as chiral ligands. The requirement for hydroxymethylene side chains in the ligands strongly suggests that bimetallic catalysts a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8023eb416be1098a7647d1f38a148d0a
https://doi.org/10.1021/ol025529a
https://doi.org/10.1021/ol025529a
Autor:
Myung-ryul Lee, Tami L. Raguse, Marina Schinnerl, William C. Pomerantz, Xiaodong Wang, Peter Wipf, Samuel H. Gellman
Publikováno v:
Organic Letters; Apr2007, Vol. 9 Issue 9, p1801-1804, 4p