Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones

Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones Full article

Journal

Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393

Output data

Year: 2010, Volume: 46, Number: 11, Pages: 1695-1701 Pages count : 7 DOI: 10.1134/S1070428010110163

Authors

Sedova V.F. ¹ , Shkurko O.P. ¹

Affiliations

1	(Данные Web of science) Russian Acad Sci, Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

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.

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

Published print:	Nov 1, 2010
Published online:	Dec 23, 2010

Web of science	WOS:000287033100016
Scopus	2-s2.0-78651327292
Elibrary	16698461
OpenAlex	W2012836304