Total synthesis of DL-crotepoxide
โ Scribed by Kengo Oda; Akitami Ichihara; Sadao Sakamura
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 176 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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๐ SIMILAR VOLUMES
We report here a stereochemically controlled total synthesis of pederamide 11) , a main hydrolysis product of the structurally unique and powerful insect C poison pederin z), in dl-form.
In the series of our investigations on total syntheses of hasubanan alkaloids, we have reported synthesis of dl-cepharamine 1 and dl-hasubanonine 2 .
Illudol, a sesquiterpene alcohol isolated from clitocybe illudens, has been characterized as 1 by Anchel et al.1. Although the stereochemistry of -\_ the sesquiterpene has not yet been reported, the structural relationship with