Total synthesis of dl-illudol
✍ Scribed by Takeshi Matsumoto; Katsuji Miyano; Shohei Kagawa; Suji Yű; Jun-ichi Ogawa; Akitami Ichihara
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 208 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
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
📜 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 .