Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 1359-1362 |
| Seitenumfang | 4 |
| Fachzeitschrift | Tetrahedron letters |
| Jahrgang | 38 |
| Ausgabenummer | 8 |
| Publikationsstatus | Veröffentlicht - 24 Feb. 1997 |
| Extern publiziert | Ja |
Abstract
The C1-C9 segment of epothilons was generated by an aldol reaction between chiral aldehyde 3 and ethyl ketone 4. Removal of the TBS protecting groups and debenzylation generated spiro ketal 13 which was analyzed by X-ray crystallography.
ASJC Scopus Sachgebiete
- Biochemie, Genetik und Molekularbiologie (insg.)
- Biochemie
- Pharmakologie, Toxikologie und Pharmazie (insg.)
- Wirkstoffforschung
- Chemie (insg.)
- Organische Chemie
Zitieren
- Standard
- Harvard
- Apa
- Vancouver
- BibTex
- RIS
in: Tetrahedron letters, Jahrgang 38, Nr. 8, 24.02.1997, S. 1359-1362.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Synthesis of the C1-C9 segment of epothilons
AU - Claus, Eckhard
AU - Pahl, Axel
AU - Jones, Peter G.
AU - Meyer, Hartmut M.
AU - Kalesse, Markus
PY - 1997/2/24
Y1 - 1997/2/24
N2 - The C1-C9 segment of epothilons was generated by an aldol reaction between chiral aldehyde 3 and ethyl ketone 4. Removal of the TBS protecting groups and debenzylation generated spiro ketal 13 which was analyzed by X-ray crystallography.
AB - The C1-C9 segment of epothilons was generated by an aldol reaction between chiral aldehyde 3 and ethyl ketone 4. Removal of the TBS protecting groups and debenzylation generated spiro ketal 13 which was analyzed by X-ray crystallography.
UR - http://www.scopus.com/inward/record.url?scp=0031584881&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(96)02493-8
DO - 10.1016/S0040-4039(96)02493-8
M3 - Article
AN - SCOPUS:0031584881
VL - 38
SP - 1359
EP - 1362
JO - Tetrahedron letters
JF - Tetrahedron letters
SN - 0040-4039
IS - 8
ER -