Details
| Original language | English |
|---|---|
| Pages (from-to) | 1790-1793 |
| Number of pages | 4 |
| Journal | Journal of natural products |
| Volume | 58 |
| Issue number | 11 |
| Publication status | Published - 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 subject areas
- Chemistry(all)
- Analytical Chemistry
- Biochemistry, Genetics and Molecular Biology(all)
- Molecular Medicine
- Pharmacology, Toxicology and Pharmaceutics(all)
- Pharmacology
- Pharmacology, Toxicology and Pharmaceutics(all)
- Pharmaceutical Science
- Pharmacology, Toxicology and Pharmaceutics(all)
- Drug Discovery
- Medicine(all)
- Complementary and alternative medicine
- Chemistry(all)
- Organic Chemistry
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In: Journal of natural products, Vol. 58, No. 11, 11.1995, p. 1790-1793.
Research output: Contribution to journal › Article › Research › 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 -