Acylation of alkynes by cationoid reagents with the formation of cyclopent-2-enone derivatives
β Scribed by A.A. Schegolev; W.A. Smit; G.V. Roitburd; V.F. Kucherov
- Book ID
- 104243032
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 243 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
We have recently described the successful use of carbocationic reagents in electiophilic additions to the triple bond and demonstrated that vinyl cations, presumably formed as intermediates in these reactions, could be trapped even by such poor nucleophilic solvents as nitromethane /I/ or chlorobenzene /2/. These results encouraged us to undertake a more thorough investigation of the reactivity of these intermediates in different solvent systems.
π SIMILAR VOLUMES
## Earlier we demonstrated that a 1,5-hydride shift readily occurs in the vinyl cation intermediate formed in the course of acylation of alkynes with acylium salts.' This paper deals with the application of this process for the preparation of a series of 1,2\_disubstituted adamantanes,
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