𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Total synthesis of methynolide

✍ 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

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

In this paper the synthesis of methynolide (1), the aglycone of methymycin, a 12‐membered macrolide antibiotic is described. We have used the chiral C‐1 to C‐8 segment 10 which has been combined with the C‐9 to C‐13 segment 9 to form the carbon skeleton of methynolide. Cyclization of the seco‐acid 14 has been accomplished by intramolecular esterification.


πŸ“œ SIMILAR VOLUMES


Highly stereoselective synthesis of meth
✍ Yuji Oikawa; Tatsuyoshi Tanaka; Osamu Yonemitsu πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 French βš– 281 KB

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.