The gas-phase ionhnolecule reactions of the CH,SCDCN, CH,SCCN and 'CH,SCDCN ions formed in the reaction of the 0-' ion with CH,SCD,CN have been studied with the use of Fourier-transform ion cyclotron resonance (FTICR). In the reaction of the CH,SCDCN carbanion with the model substrate, dimethyl disu
Reactions of carbenes with anions
✍ Scribed by Detlev Sülzle
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 117 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
CHBrC12, CHC121 and CHBr21 are prepared by a simple method based on REACTIONS OF CARBENES WITH ANIONS Detlev Siilzle the reaction of dichloro or dibromocarbene with the corresponding alkali metal halogenides under phase transfer conditions.
Although the reaction of the electrophilic carbenes /l/, Ccl2 and CBr2, with alkenes as electron rich reaction partners to prepare dihalocyclopropanes is well known, the similar reaction of these carbenes with anions, through which it is possible to prepare for example methane derivatives /2/, has been given little notice until now. This is even more surprising as the formation of dihalocarbenes in the system haloform / cont. aqueous base / phase transfer catalyst (PTC) offers an excellent opportunity to study these reactions, as the catalyst takes care of the transport of the anions across the phase boundary.
📜 SIMILAR VOLUMES
The diastereoselective Michael addition of the title anion to are formed as a result of an unexpected intramolecular transfer of an oxygen atom from the nitro group to the α-hydrogenand α-methyl-substituted conjugated nitroalkenes leads to new γ-nitrocarbene complexes and γ-hydrocarbene atom, with e