A new mode of in vitro cyclization of humulene, formation of 3,6-secoprotoilludane skeleton
β Scribed by Shyunziro Misumi; Yasufumi Ohfune; Akio Furusaki; Haruhisa Shirahama; Takeshi Matsumoto
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- French
- Weight
- 199 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
In the hypothesis of illudoids' biosynthesis2, formation of the key intermediate protoilludyl cation&has been reasonably explained by the cationic cyclization of humulene, initiated at the 4 '*lo double bond (Scheme I). However,
π SIMILAR VOLUMES
The mechanisms of the reactions of diborane with ammonia have been investigated by ab initio molecular orbital methods. The activation barrier of the formation of aminoborane, H,&NHr, from the adduct, H,B : NHs, of borane and ammonia is high (over 40 kcal/mol), because it is a reaction essentially