Structure determination of two new sesquiterpenoids from Streptomyces sanglieri
Author:
Affiliation:
1. Institute of Microbial Pharmaceuticals, College of Life and Health Sciences; Northeastern University; Shenyang China
2. Yunnan Institute of Microbiology; Yunnan University; Kunming China
Funder
National Natural Science Foundation of China
Basic Scientific Research Fund of Northeastern University, China
Publisher
Wiley
Subject
General Materials Science,General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mrc.4473/fullpdf
Reference14 articles.
1. T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes
2. Epicubenol synthase and the enzymic cyclization of farnesyl diphosphate
3. Epicubenol Synthase and the Stereochemistry of the Enzymic Cyclization of Farnesyl and Nerolidyl Diphosphate
4. Epicubenol synthase. Origin of the oxygen atom of a bacterial sesquiterpene alcohol
5. Identification of (8S,9S,10S)-8,10-Dimethyl-1-octalin, a Key Intermediate in the Biosynthesis of Geosmin in Bacteria
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