Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nadin Schläger"'
Autor:
Andreas Kirschning, Rolf Müller, Walid A. M. Elgaher, Rolf W. Hartmann, Mostafa M. Hamed, Sascha Baumann, Nadin Schläger, Maria Moreno, Jennifer Herrmann
Publikováno v:
Synlett. 26:1175-1178
The first total synthesis of cystobactamid 507, a member of a class of new natural products with strong inhibitory activity towards bacterial topoisomerases, is reported. Synthetic key challenges are the central tetrasubstitued arene and the low chem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cefa0a2a872e5a32c150279669ba49c
https://doi.org/10.1055/s-0034-1380509
https://doi.org/10.1055/s-0034-1380509
Autor:
Richard Dehn, Rolf Jansen, Rolf Müller, Nadin Schläger, Andreas Kirschning, Silke Reinecke, Klaus Gerth, Heinrich Steinmetz
Publikováno v:
Angewandte Chemie. 123:553-557
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dacd21273f34032fe435ef17c45c7d5
https://doi.org/10.1002/ange.201005226
https://doi.org/10.1002/ange.201005226
Publikováno v:
Organic letters. 16(2)
The antibiotic elansolid B1 was prepared by a convergent strategy that relied on a highly diastereoselective, biomimetic intramolecular Diels–Alder cycloaddition (IMDA) that furnished the tetrahydroindane unit. Other key features are a double Sonog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24e54a5f9534ff97f01072e5a62b0da3
https://pubmed.ncbi.nlm.nih.gov/24393030
https://pubmed.ncbi.nlm.nih.gov/24393030
Autor:
Andreas Kirschning, Nadin Schläger
Publikováno v:
Organicbiomolecular chemistry. 10(38)
The Yamamoto aldol reaction is a vinylogous aldol reaction that relies on bulky aluminium-based Lewis acids. These activate both the aldehyde as well as become part of the enolate moiety. The report discloses the first detailed study on the substrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::159019efba1192db1f2f3b7c45a0c499
https://pubmed.ncbi.nlm.nih.gov/22898755
https://pubmed.ncbi.nlm.nih.gov/22898755
Publikováno v:
Organicbiomolecular chemistry. 9(7)
Ketoreductase enzymes are responsible for the generation of hydroxyl stereocentres during the biosynthesis of complex polyketide natural products. Previous studies of isolated polyketide ketoreductases have shown that the stereospecificity of ketored
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af6d390c9985f30c897e28b71b786fc
https://pubmed.ncbi.nlm.nih.gov/21340070
https://pubmed.ncbi.nlm.nih.gov/21340070
Autor:
Andreas Kirschning, Richard Dehn, Silke Reinecke, Klaus Gerth, Rolf Jansen, Nadin Schläger, Heinrich Steinmetz, Rolf Müller
Publikováno v:
Angewandte Chemie (International ed. in English). 50(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f792b9c22bb1239bc9f1ec62ff42181b
https://pubmed.ncbi.nlm.nih.gov/21154488
https://pubmed.ncbi.nlm.nih.gov/21154488