ChemInform Abstract: New Dihydro and Tetrahydro Derivatives of Desmycosin. Part 3. The Opening of Oxirane Ring of 12,13-Epoxydesmycosin.
β Scribed by A. NARANDA; N. LOPOTAR; Z. KELNERIC
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
New Dihydro and Tetrahydro Derivatives of Desmycosin. Part 3. The Opening of Oxirane Ring of 12,13-Epoxydesmycosin.
-The catalytic hydrogenation of (I) to form (II) and the reductive oxirane-ring opening of same starting compound (I) yielding (III) fail in creating new antibacterially active derivatives. Mild acid hydrolysis of (II) gives three inactive desepoxy diols.
π SIMILAR VOLUMES
Regiochemical Control of the Ring-Opening of Epoxides by Means of Chelating Processes. Part 13. Synthesis and Ring-Opening Reactions of the Diastereoisomeric cis-and trans-Epoxides Derived from 3-(Benzyloxy)cyclopentene and 2-(Benzyloxy)-2,5-dihydrofuran. -Under standard conditions the cis-epoxides