Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones Full article
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Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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| Output data | Year: 2010, Volume: 46, Number: 11, Pages: 1695-1701 Pages count : 7 DOI: 10.1134/S1070428010110163 | ||
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Abstract:
The acetylation and chloroacetylation of 5-nitro- and 5-ethoxycarbonyl-substituted 4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones proceeds regioselectively at the N-3 atom of the heterocycle whereas the acetylation of the 5-aryloxy-substituted analog results in a mixture of N-1- and N-3-acetylated regioisomers.
Cite:
Sedova V.F.
, Shkurko O.P.
Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones
Russian Journal of Organic Chemistry. 2010. V.46. N11. P.1695-1701. DOI: 10.1134/S1070428010110163 WOS Scopus РИНЦ OpenAlex
Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones
Russian Journal of Organic Chemistry. 2010. V.46. N11. P.1695-1701. DOI: 10.1134/S1070428010110163 WOS Scopus РИНЦ OpenAlex
Dates:
| Published print: | Nov 1, 2010 |
| Published online: | Dec 23, 2010 |
Identifiers:
| Web of science: | WOS:000287033100016 |
| Scopus: | 2-s2.0-78651327292 |
| Elibrary: | 16698461 |
| OpenAlex: | W2012836304 |