Chemistry of Ginkgolides, VII. Preparation and Crystal Structure Analysis of a Secondary Ozonide from Ginkgolide A
✍ Scribed by Weinges, Klaus ;Schick, Hartmut ;Pritzkow, Hans
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 322 KB
- Volume
- 1997
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
By hydrogenation of 3,14‐didehydro‐10‐hydroxyginkgolide (3,14‐anhydroginkgolide A, 1) the 3,14‐didehydro‐10‐hydroxyginkgolide‐15‐acid (2) was obtained. Reaction with diazomethane led to the methyl ester 2a, which was transformed into its MOM derivative 2b. Ozonolysis of 2b gave a stable secondary ozonide 3 and 10‐methoxymethoxy‐3‐oxo‐14,15,16‐trinorginkgolide (4).
📜 SIMILAR VOLUMES
## Abstract Treatment of the enol acetate 3‐acetoxy‐10‐methoxy‐methoxy‐2,3‐didehydro‐14,15,16‐trinorginkgolide^[2^] (2) with potassium osmate/__N__‐methylmorpholine __N__‐oxide in acetone/acetic acid solution did not yield the expected 2‐hydroxy‐3‐oxo derivative 3, but the dimeric ginkgolide (2__S_