Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 419-422 |
| Seitenumfang | 4 |
| Fachzeitschrift | Synlett |
| Ausgabenummer | 3 |
| Publikationsstatus | Veröffentlicht - 6 Feb. 2006 |
Abstract
The enantioselective synthesis of the C1-C5 and C6-C24 fragments of the ripostatins utilize a Negishi coupling, two Nagao acetate aldol reactions followed by a Denmark vinylogous aldol reaction and Stille couplings as key C-C bond forming steps.
ASJC Scopus Sachgebiete
- Chemie (insg.)
- Organische Chemie
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in: Synlett, Nr. 3, 06.02.2006, S. 419-422.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Synthesis of the C1-C5 and C6-C24 fragments of the RNA polymerase inhibitors ripostatin A and B
AU - Kujat, Christof
AU - Bock, Martin
AU - Kirschning, Andreas
PY - 2006/2/6
Y1 - 2006/2/6
N2 - The enantioselective synthesis of the C1-C5 and C6-C24 fragments of the ripostatins utilize a Negishi coupling, two Nagao acetate aldol reactions followed by a Denmark vinylogous aldol reaction and Stille couplings as key C-C bond forming steps.
AB - The enantioselective synthesis of the C1-C5 and C6-C24 fragments of the ripostatins utilize a Negishi coupling, two Nagao acetate aldol reactions followed by a Denmark vinylogous aldol reaction and Stille couplings as key C-C bond forming steps.
KW - Antibiotics
KW - Nagao aldol reaction
KW - Natural product synthesis
KW - RNA polymerase inhibitors
KW - Vinylogous aldol reaction
UR - http://www.scopus.com/inward/record.url?scp=33344459154&partnerID=8YFLogxK
U2 - 10.1055/s-2006-926263
DO - 10.1055/s-2006-926263
M3 - Article
AN - SCOPUS:33344459154
SP - 419
EP - 422
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 3
ER -