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The formation of 1,2-disubstituted adamantanes during the acylation of monosubstituted alkynes with derivatives of 1-adamantanecarboxylic acid

โœ Scribed by M. I. Kanishchev; V. A. Smit; A. A. Shchegolev; A. P. Rodionov; R. Caple


Book ID
112438477
Publisher
Springer
Year
1979
Tongue
English
Weight
551 KB
Volume
28
Category
Article
ISSN
1573-9171

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๐Ÿ“œ SIMILAR VOLUMES


The formation of 1,2-disubstituted adama
โœ M.I. Kanischev; W.A. Smit; A.A. Schegolev; R. Caple ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 200 KB

## 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,

Acylation of alkynes by cationoid reagen
โœ A.A. Schegolev; W.A. Smit; G.V. Roitburd; V.F. Kucherov ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 243 KB

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 chlorobenz