SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs.

Wosniok, Paul R; Knopf, Christopher; Dreisigacker, Sandra; Orozco-Rodriguez, J Manuel; Hinkelmann, Bettina; Mueller, Peter P; Brönstrup, Mark; Menche, Dirk

dc.contributor.author	Wosniok, Paul R
dc.contributor.author	Knopf, Christopher
dc.contributor.author	Dreisigacker, Sandra
dc.contributor.author	Orozco-Rodriguez, J Manuel
dc.contributor.author	Hinkelmann, Bettina
dc.contributor.author	Mueller, Peter P
dc.contributor.author	Brönstrup, Mark
dc.contributor.author	Menche, Dirk
dc.date.accessioned	2020-11-16T13:54:13Z
dc.date.available	2020-11-16T13:54:13Z
dc.date.issued	2020-11-11
dc.identifier.citation	Chemistry. 2020 Nov 11. doi: 10.1002/chem.202003845. Epub ahead of print.	en_US
dc.identifier.pmid	33174290
dc.identifier.doi	10.1002/chem.202003845
dc.identifier.uri	http://hdl.handle.net/10033/622586
dc.description.abstract	Invited for the cover of this issue is the group of Dirk Menche at the University of Bonn. The image depicts the natural product leupyrrin A1 and a synthetic leupylog in balance on an IC50 weighing scale. Read the full text of the article at 10.1002/chem.202002622.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.rights	Attribution-NonCommercial-ShareAlike 4.0 International	*
dc.rights.uri	http://creativecommons.org/licenses/by-nc-sa/4.0/	*
dc.title	SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs.	en_US
dc.type	Article	en_US
dc.identifier.eissn	1521-3765
dc.contributor.department	HZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.	en_US
dc.identifier.journal	Chemistry (Weinheim an der Bergstrasse, Germany)	en_US
refterms.dateFOA	2020-11-16T13:54:14Z
dc.source.journaltitle	Chemistry (Weinheim an der Bergstrasse, Germany)
dc.source.country	Germany