Synthesis and NMR spectra of syn- and anti-tricyclo[3.2.2.02,4]non-6-ene
β Scribed by Yorke E. Rhodes; Paul E. Schueler; Victor G. DiFate
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 242 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The diamagnetic anisotropy of the double bond and long range shielding effects in n.m.r. spectra have been the subject of a number of theoretical and experimental 8tudies.l Efforts to test the predictions of the sign and
π SIMILAR VOLUMES
The addition of dihalocarbenes to norbornene and Its derivatives produces an lntermdiate which Imdergoes a cyclopropyl-ally1 rearrangement. (2) The gem-dihalocyclopropane, Isolated in
Considerable effort is being expended toward the understanding of the nature of strained carbon-carbon single bonds.2 In this respect, strained propellanes are very 1nstructive.e We wish to report syntheses for and reactivities of two new C4.2.11 propellanes; we feel the results contribute
## Abstract The ^13^C NMR spectra of tricyclo[4.2.1.0^2,5^]nonanes and tetracyclo[5.4.1.0^2,6^.0^8,11^]dodecanes and their dimethyl derivatives were measured to demonstrate the fourβmembered ring annelation effects on the bicyclo[2.2.1]heptane skeleton, and the steric Ξ΄β__syn__ effects of the methy