The chemistry of small-ring compounds. Part 51. Electron-transfer-initiated oxidation of some cyclopropylidene compounds
✍ Scribed by A. Hofland; Th. J. de Boer
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 381 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0165-0513
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📜 SIMILAR VOLUMES
Only a few examples of thermal [2+2+2] cycloadditions are reported [2] where a C-C single bond participates as a two-electron component. To our knowledge no reaction is known in which an electron-rich C-C single bond is involved In
## Abstract 1‐Hydroxy‐ and 1‐halocyclopropyl sulfides can be conveniently prepared starting from cyclopropanone. Cyclopropyl sulfides with halogen or a dimethylsulfonium group in the α‐position can be transformed into 1‐substituted cyclopropyl sulfides with a variety of nucleophiles. This means tha
## Abstract 1‐Chlorocyclopropyl methyl ether and the corresponding sulfide are methanolysed without any rupture of the three‐membered ring. The solvolysis of 1‐halocyclopropyl sulfides has been studied kinetically and takes place __via__ an __S__~N~1 mechanism. Methyl substituents in the cyclopropy
Previously we reported on the oxidation of cyclopropanols 1 by metal ions (1).