Total Synthesis of the Proposed Structure for Spirofungin B: A Reassignment of the Stereochemistry
Author:
Affiliation:
1. School of Chemistry, The University of Melbourne, Victoria 3010, Australia
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol049873e
Reference23 articles.
1. Spirofungin, a New Antifungal Antibiotic from Streptomyces violaceusniger Tue 4113.
2. Reveromycins, new inhibitors of eukaryotic cell growth. I. Producing organism, fermentation, isolation and physico-chemical properties.
3. Synthesis of the spiroacetal parts of spirofungin A and B
4. Efficient synthesis of the 6,6-spiroacetal of spirofungin A
5. Synthetic studies on reveromycin A: Stereoselective synthesis of the spiroketal system
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1. Synthesis of the spiroacetal fragments of spirofungins A and B, antibiotics isolated from Streptomyces violaceusniger Tü 4113;Heterocyclic Communications;2015-12-01
2. PdII-Catalyzed Spiroketalization of Ketoallylic Diols;Chemistry - A European Journal;2013-07-15
3. Creation of novel reveromycin derivatives by alcohol-added fermentation;The Journal of Antibiotics;2012-12-12
4. Synthesis of the Spirofungin A Core via a Domino Strategy Consisting of Olefinic Ester Ring-Closing Metathesis and Iodospiroacetalization;Synlett;2010-12-23
5. Stereoselective Total Synthesis of (−)-Spirofungin A by Utilising Hydrogen-Bond Controlled Spiroketalisation;Chemistry - A European Journal;2010-12-10
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