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Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate. / Molchanov, A. P.; Tran, T. Q.; Stepakov, A. V.; Kostikov, R. R.

In: Russian Journal of Organic Chemistry, Vol. 52, No. 11, 01.11.2016, p. 1603-1605.

Research output: Contribution to journal › Article › peer-review

Harvard

Molchanov, AP, Tran, TQ, Stepakov, AV & Kostikov, RR 2016, 'Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate', Russian Journal of Organic Chemistry, vol. 52, no. 11, pp. 1603-1605. https://doi.org/10.1134/S1070428016110099, https://doi.org/10.1134/S1070428016110099

APA

Molchanov, A. P., Tran, T. Q., Stepakov, A. V., & Kostikov, R. R. (2016). Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate. Russian Journal of Organic Chemistry, 52(11), 1603-1605. https://doi.org/10.1134/S1070428016110099, https://doi.org/10.1134/S1070428016110099

Vancouver

Molchanov AP, Tran TQ, Stepakov AV, Kostikov RR. Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate. Russian Journal of Organic Chemistry. 2016 Nov 1;52(11):1603-1605. https://doi.org/10.1134/S1070428016110099, https://doi.org/10.1134/S1070428016110099

Author

Molchanov, A. P. ; Tran, T. Q. ; Stepakov, A. V. ; Kostikov, R. R. / Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate. In: Russian Journal of Organic Chemistry. 2016 ; Vol. 52, No. 11. pp. 1603-1605.

BibTeX

@article{e3d6c090265f479a8aa152699db3e4fe,
title = "Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate",
abstract = "Oxidation with 2,3-dichloro-4,5-dicyanobenzoquinone of 2,4-dihydro-1Н-azeto[1,2-a]quinoline-3,4 -dicarboxylates obtained in the reaction of N-aryl-С,С-disubstituted nitrones with Feist{\textquoteright}s acid ester resulted in the formation of 2-vinylquinoline-3,4-dicarboxylates in good yields.",
author = "Molchanov, {A. P.} and Tran, {T. Q.} and Stepakov, {A. V.} and Kostikov, {R. R.}",
note = "Publisher Copyright: {\textcopyright} 2016, Pleiades Publishing, Ltd. Copyright: Copyright 2017 Elsevier B.V., All rights reserved.",
year = "2016",
month = nov,
day = "1",
doi = "10.1134/S1070428016110099",
language = "English",
volume = "52",
pages = "1603--1605",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "11",

}

RIS

TY - JOUR

T1 - Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate

AU - Molchanov, A. P.

AU - Tran, T. Q.

AU - Stepakov, A. V.

AU - Kostikov, R. R.

N1 - Publisher Copyright: © 2016, Pleiades Publishing, Ltd. Copyright: Copyright 2017 Elsevier B.V., All rights reserved.

PY - 2016/11/1

Y1 - 2016/11/1

N2 - Oxidation with 2,3-dichloro-4,5-dicyanobenzoquinone of 2,4-dihydro-1Н-azeto[1,2-a]quinoline-3,4 -dicarboxylates obtained in the reaction of N-aryl-С,С-disubstituted nitrones with Feist’s acid ester resulted in the formation of 2-vinylquinoline-3,4-dicarboxylates in good yields.

AB - Oxidation with 2,3-dichloro-4,5-dicyanobenzoquinone of 2,4-dihydro-1Н-azeto[1,2-a]quinoline-3,4 -dicarboxylates obtained in the reaction of N-aryl-С,С-disubstituted nitrones with Feist’s acid ester resulted in the formation of 2-vinylquinoline-3,4-dicarboxylates in good yields.

UR - http://www.scopus.com/inward/record.url?scp=85010049811&partnerID=8YFLogxK

U2 - 10.1134/S1070428016110099

DO - 10.1134/S1070428016110099

M3 - Article

AN - SCOPUS:85010049811

VL - 52

SP - 1603

EP - 1605

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 11

ER -

ID: 9291096