Abstract
Reactions of 2-trichloromethylchromones with ethylenediamine at room temperature give 2-(2-hydroxyaroylmethylene)imidazolidines in high yields.
References
1.
10.1070/MC1999v009n05ABEH001110_bib1
Ostroumov
Zh. Org. Khim.,
1988
2.
Sosnovskikh V.Y., Mel’nikov M.Y.
Mendeleev Communications,
1998
3.
10.1070/MC1999v009n05ABEH001110_bib3
Nair
Indian J. Chem.,
1982
4.
Merchant J.R., Bhat A.R., Rege D.V.
Tetrahedron Letters,
1972
5.
10.1070/MC1999v009n05ABEH001110_bib5
Sosnovskikh
Zh. Org. Khim.,
1993
6.
10.1070/MC1999v009n05ABEH001110_bib6
Zagorevskii
Zh. Obshch. Khim.,
1960
7.
10.1070/MC1999v009n05ABEH001110_bib7
Saloutin
Izv. Akad. Nauk, Ser. Khim.,
1994
8.
10.1070/MC1999v009n05ABEH001110_bib8
Owczarek
Pol. J. Chem.,
1991
9.
10.1070/MC1999v009n05ABEH001110_bib9
Sosnovskikh
Izv. Akad. Nauk, Ser. Khim.,
1999
10.
V. Ya. Sosnovskikh, M. Yu. Mel’nikov and I. I. Vorontsov. unpublished data.
11.
Schiøtt B., Iversen B.B., Hellerup Madsen G.K., Bruice T.C.
Journal of the American Chemical Society,
1998
12.
10.1070/MC1999v009n05ABEH001110_bib12
Sosnovskikh
Izv. Akad. Nauk, Ser. Khim.,
1998
13.
Coenen M., Faust J., Ringel C., Mayer R.
Journal für praktische Chemie,
1965
14.
10.1070/MC1999v009n05ABEH001110_bib14
Belen’kii
Khim. Geterotsikl. Soedin.,
1993
15.
Wald D.K., Joullié M.M.
Journal of Organic Chemistry,
1966
16.
Salim J.R., Nome F., Rezende M.C.
Synthetic Communications,
1989
17.
Hess S.C., Nome F., Zucco C., Rezende M.C.
Synthetic Communications,
1989