Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 1264-1268 |
| Seitenumfang | 5 |
| Fachzeitschrift | Synlett |
| Ausgabenummer | 8 |
| Publikationsstatus | Veröffentlicht - 18 Apr. 2007 |
Abstract
The enantioselective synthesis of two new proansamitocin derivatives is described. Macrocyclization is achieved by ring-closing metathesis of appropriate alkene and diene precursors.
ASJC Scopus Sachgebiete
- Chemie (insg.)
- Organische Chemie
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in: Synlett, Nr. 8, 18.04.2007, S. 1264-1268.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Total syntheses of new proansamitocin derivatives by ring-closing metathesis
AU - Meyer, Axel
AU - Kirschning, Andreas
PY - 2007/4/18
Y1 - 2007/4/18
N2 - The enantioselective synthesis of two new proansamitocin derivatives is described. Macrocyclization is achieved by ring-closing metathesis of appropriate alkene and diene precursors.
AB - The enantioselective synthesis of two new proansamitocin derivatives is described. Macrocyclization is achieved by ring-closing metathesis of appropriate alkene and diene precursors.
KW - Ansamitocins
KW - Macrolactam antibiotics
KW - Natural product synthesis
KW - Ring-closing metathesis
UR - http://www.scopus.com/inward/record.url?scp=34249795484&partnerID=8YFLogxK
U2 - 10.1055/s-2007-977441
DO - 10.1055/s-2007-977441
M3 - Article
AN - SCOPUS:34249795484
SP - 1264
EP - 1268
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 8
ER -