A synthesis of tricyclo[3.3.0.03,7]Octane (bisnoradamantane); solvolysis of its mono and dicarbinols
β Scribed by B.Richard Vogt; Stuart R. Suter; John R.E. Hoover
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 220 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
We wish to report the synthesis of tricyclo[3.3.0.03'7 ]octane (I) by a structurally unambiguous route and to describe the ring expansion of the derived carbinols II and III. Hydrocarbon I, for which we suggest the trivial name %isnoradamantane", may be regarded as a lower homolog of adamantane (IV), derived from IV by the deletion of two oppositely situated methylene bridges:
π SIMILAR VOLUMES
Our interest in the hydrocarbon tricyclo[3.3.0.0Jt7 Ioctane (l) has been stimulated by its bisnor relationship to adamantane (zero carbon bridges between C-l-C-5 and C-3-C-7 rather than one carbon bridges), its symmetry (Dad) and the fact that it contains the most twisted norbornane skeleton of reco
THE SYNTHESIS 0F ~~rc~~~o[4.3.1.03'~]D~xx~~ (ISOADAMANTANE) AND SOLVOLYSIS OF ITS CJ-CARBINOL
Reaction of kinetic enolate of a H -substituted cyclohexenone derivatives with vinylselenoxides provided tricyclo[3.2.1.0 2,7 ]octane-6-one derivatives via domino Michael-Michael-substitution protocol.