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Mendeleev Communications, 1993, Volume 3, Issue 5, Pages 188–189
DOI: https://doi.org/10.1070/MC1993v003n05ABEH000280 (Mi mendc5323) 		 
This article is cited in 21 scientific papers (total in 21 papers)

Carbonylation of Cyclopentane in the Presence of Aprotic Organic Superacids

I. S. Akhrem, S. Z. Bernadyuk, M. E. Vol'pin

A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (289 kB) Citations (21)
DOI: https://doi.org/10.1070/MC1993v003n05ABEH000280
Abstract: The systems MeCOBr·nAlBr3 as well as CHBr3·nAlBr3 and CCl4·nAlBr3 (n =1-4.5) have been shown to initiate carbonylation of cyclopentane under mild conditions to give, after alcoholic work-up, the corresponding ester of cyclopentylcarboxylic acid with good yields and high selectivity.
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Document Type: Article
Language: English


Citation: I. S. Akhrem, S. Z. Bernadyuk, M. E. Vol'pin, “Carbonylation of Cyclopentane in the Presence of Aprotic Organic Superacids”, Mendeleev Commun., 3:5 (1993), 188–189
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    • This publication is cited in the following 21 articles:
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