doping-addition" of 2-N02C6H4SG1 to the tricyclo[4,2,2,0295]deca-3,7,+trj\_ene system ~\_occurs to give unusual products: (i) rearanged caged cyclopropane Aand (ii) the stable cross-PerChlOrate &
β¦ LIBER β¦
Novel skeletal rearrangement in addition reaction to tricyclo[4,2,2,02,5]deca-3,7-diene system
β Scribed by Nicolai S. Zefirov; V.N. Kirin; A.S. Kozmin; I.V. Bodrikov; K.A. Potekhin; E.N. Kurkutova
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 206 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The "doping-a,-Jdition" of RSCl to the tricyclo[4,2,2,0 2,51 ~deca-3,7-diene derivatives which are incapable of lactone ring closure proceeds to give the 'love1 type of rec3rranged product, x, due to the two subsequent 1,2-shifts.
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## 500001 (India) New syntheses of tricycle [4.2.2.0285] deca-3,7-dien-g-one are described. Direct and sensftised photolysis of this ring system provides facile entry to several novel polycyclic~.