Total synthesis of methynolide
β Scribed by Ditrich, Klaus
- Book ID
- 102901327
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 527 KB
- Volume
- 1990
- Category
- Article
- ISSN
- 0947-3440
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β¦ Synopsis
Abstract
In this paper the synthesis of methynolide (1), the aglycone of methymycin, a 12βmembered macrolide antibiotic is described. We have used the chiral Cβ1 to Cβ8 segment 10 which has been combined with the Cβ9 to Cβ13 segment 9 to form the carbon skeleton of methynolide. Cyclization of the secoβacid 14 has been accomplished by intramolecular esterification.
π SIMILAR VOLUMES
A highly stereoselective and efficient synthesis of methynolide, the aglycone of 12membered macrolide methymycin, was achieved from of Cl-C8 and C9-Cl3 segments synthesized from D-glucose by employing some stereoselective reactions and benzyl-type protecting groups.