Standard

Facile synthesis of pyrido[2,3-d]pyrimidines via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with β-substituted β-aminoacrylic esters. / Chizhova, M.E.; Bakulina, O.Yu.; Ivanov, A.Yu.; Lobanov, P.S.; Dar'in, D.V.

в: Tetrahedron, Том 71, № 36, 2015, стр. 6196-6203.

Результаты исследований: Научные публикации в периодических изданиях › статья

Harvard

Chizhova, ME, Bakulina, OY, Ivanov, AY, Lobanov, PS & Dar'in, DV 2015, 'Facile synthesis of pyrido[2,3-d]pyrimidines via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with β-substituted β-aminoacrylic esters', Tetrahedron, Том. 71, № 36, стр. 6196-6203. https://doi.org/10.1016/j.tet.2015.06.085

APA

Chizhova, M. E., Bakulina, O. Y., Ivanov, A. Y., Lobanov, P. S., & Dar'in, D. V. (2015). Facile synthesis of pyrido[2,3-d]pyrimidines via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with β-substituted β-aminoacrylic esters. Tetrahedron, 71(36), 6196-6203. https://doi.org/10.1016/j.tet.2015.06.085

Vancouver

Chizhova ME, Bakulina OY, Ivanov AY, Lobanov PS, Dar'in DV. Facile synthesis of pyrido[2,3-d]pyrimidines via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with β-substituted β-aminoacrylic esters. Tetrahedron. 2015;71(36):6196-6203. https://doi.org/10.1016/j.tet.2015.06.085

Author

Chizhova, M.E. ; Bakulina, O.Yu. ; Ivanov, A.Yu. ; Lobanov, P.S. ; Dar'in, D.V. / Facile synthesis of pyrido[2,3-d]pyrimidines via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with β-substituted β-aminoacrylic esters. в: Tetrahedron. 2015 ; Том 71, № 36. стр. 6196-6203.

BibTeX

@article{d715ae8b14704db08a9caf3e8da18dc2,
title = "Facile synthesis of pyrido[2,3-d]pyrimidines via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with β-substituted β-aminoacrylic esters",
abstract = "A new facile synthesis of pyrido[2,3-d]pyrimidin-4-ones via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with beta-alkyl and beta-aryl-beta-aminoacrylic esters followed by hydrolysis of chlorine atom at position 4 of pyridopyrimidine ring has been developed. The cyclocondensation was found to be accelerated by acid. (C) 2015 Elsevier Ltd. All rights reserved.",
author = "M.E. Chizhova and O.Yu. Bakulina and A.Yu. Ivanov and P.S. Lobanov and D.V. Dar'in",
year = "2015",
doi = "10.1016/j.tet.2015.06.085",
language = "English",
volume = "71",
pages = "6196--6203",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier",
number = "36",

}

RIS

TY - JOUR

T1 - Facile synthesis of pyrido[2,3-d]pyrimidines via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with β-substituted β-aminoacrylic esters

AU - Chizhova, M.E.

AU - Bakulina, O.Yu.

AU - Ivanov, A.Yu.

AU - Lobanov, P.S.

AU - Dar'in, D.V.

PY - 2015

Y1 - 2015

N2 - A new facile synthesis of pyrido[2,3-d]pyrimidin-4-ones via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with beta-alkyl and beta-aryl-beta-aminoacrylic esters followed by hydrolysis of chlorine atom at position 4 of pyridopyrimidine ring has been developed. The cyclocondensation was found to be accelerated by acid. (C) 2015 Elsevier Ltd. All rights reserved.

AB - A new facile synthesis of pyrido[2,3-d]pyrimidin-4-ones via cyclocondensation of 4,6-dichloro-2-methylsulfanylpyrimidine-5-carbaldehyde with beta-alkyl and beta-aryl-beta-aminoacrylic esters followed by hydrolysis of chlorine atom at position 4 of pyridopyrimidine ring has been developed. The cyclocondensation was found to be accelerated by acid. (C) 2015 Elsevier Ltd. All rights reserved.

U2 - 10.1016/j.tet.2015.06.085

DO - 10.1016/j.tet.2015.06.085

M3 - Article

VL - 71

SP - 6196

EP - 6203

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 36

ER -

ID: 3974625