Formal Total Synthesis of Enantiopure (-)-Anisomycin, Antibiotic from Streptomyces. -Starting from easily available, enantiopure, dual purpose inductor (I) highly enantioselective formal total synthesis of (-)-anisomycin (X) is achieved in approximately 8% overall yield. It is based on an effective
ChemInform Abstract: Total Synthesis of Rutamycin B (I), a Macrolide Antibiotic from Streptomyces aureofaciens.
β Scribed by James D. White; Roger Hanselmann; Randy W. Jackson; Warren J. Porter; Yoshihiro Ohba; Thomas Tiller; Shan Wang
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 26 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Total Synthesis of 10-Deoxymethynolide, the Aglycon of the Macrolide Antibiotic 10-Deoxymethymycin. -The title compound (XI) is prepared in 12% overall yield via a synthetic equivalent (VIII) of the Prelog-Djerassi lactonic acid and the construction of a 12-membered lactone through an intramolecula