Research output: Contribution to journal › Article
CHEMOSELECTIVE CYCLOCONDENSATION OF Α-ACYLACETAMIDINES WITH 2-METHYLSULFANYL-4,6-DICHLOROPYRIMIDINE-5-CARBALDEHYDE. / Ryazanov, S.G.; Selivanov, S.I.; Dar’in, D.V.; Lobanov, P.S.; Potekhin, A.A.
In: Russian Journal of Organic Chemistry, No. 2, 2008, p. 288-291.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - CHEMOSELECTIVE CYCLOCONDENSATION OF Α-ACYLACETAMIDINES WITH 2-METHYLSULFANYL-4,6-DICHLOROPYRIMIDINE-5-CARBALDEHYDE
AU - Ryazanov, S.G.
AU - Selivanov, S.I.
AU - Dar’in, D.V.
AU - Lobanov, P.S.
AU - Potekhin, A.A.
PY - 2008
Y1 - 2008
N2 - 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. © 2008 MAIK Nauka.
AB - 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. © 2008 MAIK Nauka.
M3 - Article
SP - 288
EP - 291
JO - Russian Journal of Organic Chemistry
JF - Russian Journal of Organic Chemistry
SN - 1070-4280
IS - 2
ER -
ID: 5264760