Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 1790-1793 |
| Seitenumfang | 4 |
| Fachzeitschrift | Journal of natural products |
| Jahrgang | 58 |
| Ausgabenummer | 11 |
| Publikationsstatus | Veröffentlicht - Nov. 1995 |
Abstract
Separation of an extract of Streptomyces citreus CBS 109.60 by column chromatography and preparative gas chromatography yielded the novel sesquiterpene alcohol 1, whose structure and relative conformation were established by spectroscopic means. Comparison of the its spectral data with compounds of known absolute configuration led to assignment of the stereochemistry at C-4 and C-7. Thus, 1 was assigned as 4S, 7R-germacra-1(10)E, 5E-diene-1 1-ol.
ASJC Scopus Sachgebiete
- Chemie (insg.)
- Analytische Chemie
- Biochemie, Genetik und Molekularbiologie (insg.)
- Molekularmedizin
- Pharmakologie, Toxikologie und Pharmazie (insg.)
- Pharmakologie
- Pharmakologie, Toxikologie und Pharmazie (insg.)
- Pharmazeutische Wissenschaften
- Pharmakologie, Toxikologie und Pharmazie (insg.)
- Wirkstoffforschung
- Medizin (insg.)
- Ergänzende und alternative Medizin
- Chemie (insg.)
- Organische Chemie
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in: Journal of natural products, Jahrgang 58, Nr. 11, 11.1995, S. 1790-1793.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - A sesquiterpene alcohol from streptomyces citreus cbs 109.60
AU - GanβEr, Dietmar
AU - Pollak, Frauke C.
AU - Berger, Ralf G.
PY - 1995/11
Y1 - 1995/11
N2 - Separation of an extract of Streptomyces citreus CBS 109.60 by column chromatography and preparative gas chromatography yielded the novel sesquiterpene alcohol 1, whose structure and relative conformation were established by spectroscopic means. Comparison of the its spectral data with compounds of known absolute configuration led to assignment of the stereochemistry at C-4 and C-7. Thus, 1 was assigned as 4S, 7R-germacra-1(10)E, 5E-diene-1 1-ol.
AB - Separation of an extract of Streptomyces citreus CBS 109.60 by column chromatography and preparative gas chromatography yielded the novel sesquiterpene alcohol 1, whose structure and relative conformation were established by spectroscopic means. Comparison of the its spectral data with compounds of known absolute configuration led to assignment of the stereochemistry at C-4 and C-7. Thus, 1 was assigned as 4S, 7R-germacra-1(10)E, 5E-diene-1 1-ol.
UR - http://www.scopus.com/inward/record.url?scp=0029586268&partnerID=8YFLogxK
U2 - 10.1021/np50125a027
DO - 10.1021/np50125a027
M3 - Article
AN - SCOPUS:0029586268
VL - 58
SP - 1790
EP - 1793
JO - Journal of natural products
JF - Journal of natural products
SN - 0163-3864
IS - 11
ER -