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Mendeleev Communications, 2003, Volume 13, Issue 2, Pages 82–84
DOI: https://doi.org/10.1070/MC2003v013n02ABEH001618 (Mi mendc3968) 		 
This article is cited in 7 scientific papers (total in 7 papers)

The Ritter reaction mechanism: new corroboration in the synthesis of arylsulfonyl(thio)propionic acid N-(1-adamantyl)amides

N. P. Gerasimova, N. A. Nozhnin, V. V. Ermolaeva, A. V. Ovchinnikova, Yu. A. Moskvichev, E. M. Alov, A. S. Danilova

Department of Chemical Technology, Yaroslavl State Technical University, Yaroslavl, Russian Federation
Full-text PDF (103 kB) Citations (7)
DOI: https://doi.org/10.1070/MC2003v013n02ABEH001618
Abstract: Pure intermediates in the Ritter reactions between adamantan-1-ol and arylsulfonyl(thio)propionitriles were isolated and identified for the first time.
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Document Type: Article
Language: English


Citation: N. P. Gerasimova, N. A. Nozhnin, V. V. Ermolaeva, A. V. Ovchinnikova, Yu. A. Moskvichev, E. M. Alov, A. S. Danilova, “The Ritter reaction mechanism: new corroboration in the synthesis of arylsulfonyl(thio)propionic acid N-(1-adamantyl)amides”, Mendeleev Commun., 13:2 (2003), 82–84
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  • https://www.mathnet.ru/eng/mendc/v13/i2/p82
    • This publication is cited in the following 7 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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