## Abstract The carbon and proton NMR spectra of __syn__‐ and __anti__‐tricyclo[5.1.0.0^3,5^]octanes and their dichlorocarbene CH 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
Reaction of duroquinone with diazomethane: Formation of tricyclo[5,1,0,03,5]octane derivatives
✍ Scribed by W.C. Howell; M. Ktenas; J.M. MacDonald
- Book ID
- 104240764
- Publisher
- Elsevier Science
- Year
- 1964
- Tongue
- French
- Weight
- 246 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
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 duroquinone. New structural formulas are assigned to each of the compounds arising from the reaction and a convenient method is elaborated for the synthesis of potentially interesting derivatives of the little-known
📜 SIMILAR VOLUMES
**Reaktionen von 1,3,5,7‐Tetramethyl‐__anti__‐tricyclo[5.1.0.0^3,5^]octan‐2,6‐diolen und deren 4,4,8,8‐Tetrachlor‐ und 4,8‐Dichlorderivaten mit Diphosphortetrajodid** Es wurden die P~2~I~4~‐Reaktionen mit 1,3,5,7‐Tetramethyl‐__anti__‐tricyclo[5.1.0.0^3,5^]‐octan‐2,6‐diolen (**3**/**6**), mit dem 4,