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Three polyhalogenated tricyclo[5.1.0.03,5]octane compounds

✍ Scribed by Lynch, V. M. ;Baran Jnr, J. R. ;Lagow, R. J. ;Davis, B. E.


Book ID
114511164
Publisher
International Union of Crystallography
Year
1994
Tongue
English
Weight
383 KB
Volume
50
Category
Article
ISSN
0108-2701

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πŸ“œ SIMILAR VOLUMES


Tricyclo[5.1.0.03.5]octan-2-ols
✍ Lambert, Joseph B.; Koeng, Fred R.; Hamersma, J. Warren πŸ“‚ Article πŸ“… 1971 πŸ› American Chemical Society 🌐 English βš– 834 KB
trans-Tricyclo[5.1.0.01,3]octane
✍ Miebach, Thomas; Brinker, Udo H. πŸ“‚ Article πŸ“… 1993 πŸ› American Chemical Society 🌐 English βš– 188 KB
Reaction of duroquinone with diazomethan
✍ W.C. Howell; M. Ktenas; J.M. MacDonald πŸ“‚ Article πŸ“… 1964 πŸ› Elsevier Science 🌐 French βš– 246 KB

It has been reported previously (1) that duroquinone, in contrast to many other p-quinones (2,3), reacts with diazomethane by direct addition at the carbonyl groups. We have reinvestigated this system and find that, in fact, the reaction proceeds bJ addition to the olefinic centres of the duroquinon

Proton NMR studies of syn- and anti-tric
✍ Linxiao Xu; Udo H. Brinker; William B. Smith πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 528 KB

## Abstract The carbon and proton NMR spectra of __syn__‐ and __anti__‐tricyclo[5.1.0.0^3,5^]octanes and their dichlorocarbene Cο£ΏH bond insertion products were determined by conventional 1D and 2D methods. Partially relaxed proton spectroscopy was carried out in some instances to aid in the separat