Chemoselective cyclocondensation of α-acylacetamidines with 2-methylsulfanyl-4,6-dichloropyrimidine-5-carbaldehyde
Cyclocondensation of α-acylacetamidine with 2-methylsulfanyl-4,6-dichloropyrimidine-5-carbaldehyde proceeds chemo- and regioselectively involving replacement by the α-carbon of the amidine of the chlorine in the aromatic ring and a reaction of the amino group with the formyl group.
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| Veröffentlicht in: | Russian journal of organic chemistry 2008, Vol.44 (2), p.288-291 |
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| container_end_page | 291 |
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| container_issue | 2 |
| container_start_page | 288 |
| container_title | Russian journal of organic chemistry |
| container_volume | 44 |
| creator | Ryazanov, S. G Selivanov, S. I Dar'in, D. V Lobanov, P. S Potekhin, A. A |
| description | Cyclocondensation of α-acylacetamidine with 2-methylsulfanyl-4,6-dichloropyrimidine-5-carbaldehyde proceeds chemo- and regioselectively involving replacement by the α-carbon of the amidine of the chlorine in the aromatic ring and a reaction of the amino group with the formyl group. |
| doi_str_mv | 10.1134/S1070428008020176 |
| format | Article |
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| identifier | ISSN: 1070-4280 |
| ispartof | Russian journal of organic chemistry, 2008, Vol.44 (2), p.288-291 |
| issn | 1070-4280 1608-3393 |
| language | eng |
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| source | SpringerLink Journals |
| subjects | Chemistry Chemistry and Materials Science Organic Chemistry |
| title | Chemoselective cyclocondensation of α-acylacetamidines with 2-methylsulfanyl-4,6-dichloropyrimidine-5-carbaldehyde |
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