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Organoboron compounds 336. The reaction of 1,3,3-trimethylcyclopropene with triallylborane

โœ Scribed by Yu. N. Bubnov; B. A. Kazanskii; O. A. Nesmeyanova; T. Yu. Rudashevskaya; B. M. Mikhailov


Book ID
112447853
Publisher
Springer
Year
1977
Tongue
English
Weight
342 KB
Volume
26
Category
Article
ISSN
1573-9171

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๐Ÿ“œ SIMILAR VOLUMES


Evidence for a carbonium ion rearrangeme
โœ Herman G. Richey Jr.; Barry Kubala; Mark A. Smith ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 212 KB

Formation of acyclic products in the reaction of triisobutylaluminum and 1,3,3trimethylcyclopropene can reasonably be ascribed to a carbonium ion rearrangement. This suggestion supports the mechanism for carbalumination of alkenes proposed by Eisch.