Nucleophilic substitution of chloro-substituted enaminones that are derivatives of imidazolidine nitroxides - The catalytic effect of the cyanide ion Full article
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European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690 |
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| Output data | Year: 2003, Volume: 2003, Number: 18, Pages: 3599-3602 Pages count : DOI: 10.1002/ejoc.200200722 | ||||
| Tags | enaminones; nitrogen heterocycles; nitroxides; nucleophilic substitution | ||||
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Abstract:
The cyanide ion is a catalyst for reactions of nucleophiles with chloro-substituted enaminones derived from imidazolidine nitroxides, which result in the formation of formal nucleophilic substitution products. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.
Cite:
Roshchupkina G.
, Rybalova T.
, Gatilov Y.
, Reznikov V.
Nucleophilic substitution of chloro-substituted enaminones that are derivatives of imidazolidine nitroxides - The catalytic effect of the cyanide ion
European Journal of Organic Chemistry. 2003. V.2003. N18. P.3599-3602. DOI: 10.1002/ejoc.200200722 WOS Scopus РИНЦ OpenAlex
Nucleophilic substitution of chloro-substituted enaminones that are derivatives of imidazolidine nitroxides - The catalytic effect of the cyanide ion
European Journal of Organic Chemistry. 2003. V.2003. N18. P.3599-3602. DOI: 10.1002/ejoc.200200722 WOS Scopus РИНЦ OpenAlex
Dates:
| Published print: | Sep 1, 2003 |
Identifiers:
| Web of science: | WOS:000185592300013 |
| Scopus: | 2-s2.0-0141504440 |
| Elibrary: | 13435518 |
| OpenAlex: | W2028047562 |