The thermolysis of 3-methylenebicyclo[3.2.1]oct-6-ene and of 3-oxobicyclo[3.2.1]oct-6-ehe
โ Scribed by J. Japenga; M. Kool; G.W. Klumpp
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 114 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
In connection with our work on the thermal 1.3-carbon shifts of bicyclo[3.2.n1 alka-2,6-dienes (n = 1,2; cf. I+II)' we have also examined the thermal behaviour of 3-methylenebicgclo[3.2.l]oct-6-ene (IIIa)2 and of 3-oxobicyclo[3.2.1}act-6-ene (IIIb)3, which contain a double bond at C-3 in the exocyclic position. The study of these compounds is also of interest with regard to recent work on the structurally related 1.5-hexadiene derivatives IV -VI?,5
๐ SIMILAR VOLUMES
3+2)Cycloaddition of alkynes to ally1 cations, generated from 3-chlorocyclohexenes and zinc chloride, provides a simple and direct route to bicyclo[3.2.l]oct-6-enes. Bicyclo[3.2.l]octane derivatives are of interest because of their occurrence in natural product structures , many of which are of biol
The l,J-dipolar cycle-additions of organic asides to strained cyclic olefins are well documented. Phenyl azide $92 and ethyl asidof'ormate3 are known to undergo stereoselective
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