Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Roman Hanke"'
Autor:
Martin Melchers, Sabine Hohmann, Oliver Gutbrod, Christian Arnold, Hans-Peter Thiesen, Isabelle Adelt, Udo Reckmann, Jutta Böhmer, Roman Hanke, Horst Antonicek, Patricia Behrmann, Olga Malsam, Peter Lösel, Elisabeth Peschel, Valentina Neufert, Marc van Houtdreve, Thomas Schenke, Nicole Blaha, Jens Frackenpohl, Hans-Christoph Weiss, Kathrin Vogelsang, Robert Velten
Publikováno v:
Bioorganic & Medicinal Chemistry. 17:4160-4184
Starting from natural product podophyllotoxin 1 substituted heterolignans were identified with promising insecticidal in vivo activity. The impact of substitution in each segment of the core structure was investigated in a detailed SAR study, and var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75befe152bcd1d56e13746510629d71c
https://doi.org/10.1016/j.bmc.2009.01.042
https://doi.org/10.1016/j.bmc.2009.01.042
Publikováno v:
European Journal of Organic Chemistry. 2004:2783-2790
The Interleukin-6 (IL-6) responsive JAK/STAT pathway seems to be correlated with major diseases such as chronic inflammation, arteriosclerosis, liver fibrosis, Parkinson and Alzheimer disease. In order to take a look at (−)-galiellalactone as a pot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3feea5141234679cd46d5245e4696db
https://doi.org/10.1002/ejoc.200400137
https://doi.org/10.1002/ejoc.200400137
Autor:
Frank-Ulrich Geschke, Rainer Endermann, Roman Hanke, Heidi Theis, Lars Johannsen, Joachim Rudolph
Publikováno v:
Journal of medicinal chemistry. 44(4)
seco-Cyclothialidines are a promising class of bacterial DNA gyrase B subunit inhibitors. A new seco-cyclothialidine derivative containing a dioxazine moiety, BAY 50-7952, was synthesized through a new concise pathway. One key step of the synthesis i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::136841cad5f65bbac405c98dc192c69f
https://pubmed.ncbi.nlm.nih.gov/11170652
https://pubmed.ncbi.nlm.nih.gov/11170652
Autor:
Roger Kaese, Joachim Rudolph, Achim May, Ralf Wischnat, Undine Zuther, Roman Hanke, Heidi Theis
Publikováno v:
Tetrahedron Letters. 44:4393-4394
An efficient scalable synthesis of 2-halothiazolium-type peptide coupling reagents has been developed. The key step is the formation of the 2-bromothiazole scaffold through cyclization of α-thiocyanato ketones with hydrogen bromide. Using this metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c29c3731e018b3117f81941f60f96f18
https://doi.org/10.1016/s0040-4039(03)00928-6
https://doi.org/10.1016/s0040-4039(03)00928-6
Publikováno v:
European Journal of Organic Chemistry. 2004:2753-2753
The cover picture shows a further chapter in the excitingDiels−Alder story around the natural product (−)-galiellalactone. This story started with Steglich′s proposal on the Diels−Alder biosynthesis of galiellalactone, that was then experimen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6861e62feb810b2c5645bb49e64fe753
https://doi.org/10.1002/ejoc.200490026
https://doi.org/10.1002/ejoc.200490026
Autor:
Roman Hankeln
Publikováno v:
De Musica Disserenda, Vol 9, Iss 1-2, Pp 191-207 (2015)
It is significant for medieval Latin liturgical texts (including plainchant texts) that early Christian authors adopted the language of war and heroism in a metaphorical sense to describe the character and behavior of the saints, and especially of ma
Externí odkaz:
https://doaj.org/article/39c9bde503de4128bc91578ad646c0c3
Publikováno v:
European Journal of Organic Chemistry; Jul2004, Vol. 2004 Issue 13, p2753-2753, 1p