The ginkgolides. III. The structure of the ginkgolides
✍ Scribed by M. Maruyama; A. Terahara; Y. Nakadaira; M. C. Woods; K. Nakanishi
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 237 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
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## Abstract 3,14‐Didehydro‐10‐hydroxyginkgolideOn the nomenclature: The skeleton of the ginkgolides A, B, C, M and J with the natural configuration is called “ginkgolide” since the systematic IUPAC nomenclature is too complicated. According to our nomenclature ginkgolide “A” is 3,10‐dihydroxyginkgo
## 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