Standard

Formation of 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine. / Gein, V. L.; Yankin, A. N.; Nosova, N. V.; Dmitriev, M. V.; Nasakin, O. E.

в: Russian Journal of General Chemistry, Том 86, № 1, 01.01.2016, стр. 58-61.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Gein, VL, Yankin, AN, Nosova, NV, Dmitriev, MV & Nasakin, OE 2016, 'Formation of 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine', Russian Journal of General Chemistry, Том. 86, № 1, стр. 58-61. https://doi.org/10.1134/S1070363216010114

APA

Gein, V. L., Yankin, A. N., Nosova, N. V., Dmitriev, M. V., & Nasakin, O. E. (2016). Formation of 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine. Russian Journal of General Chemistry, 86(1), 58-61. https://doi.org/10.1134/S1070363216010114

Vancouver

Gein VL, Yankin AN, Nosova NV, Dmitriev MV, Nasakin OE. Formation of 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine. Russian Journal of General Chemistry. 2016 Янв. 1;86(1):58-61. https://doi.org/10.1134/S1070363216010114

Author

Gein, V. L. ; Yankin, A. N. ; Nosova, N. V. ; Dmitriev, M. V. ; Nasakin, O. E. / Formation of 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine. в: Russian Journal of General Chemistry. 2016 ; Том 86, № 1. стр. 58-61.

BibTeX

@article{1d23b5a0182b4aa4b752becdce0be8ef,
title = "Formation of 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine",
abstract = "Reactions of acetoacetanilide with aromatic aldehydes in ethanol at room temperature in the presence of molecular iodine and arylamine afford to 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides. The structure of obtained compounds was confirmed by mass spectrometry, IR and NMR spectroscopy data.",
keywords = "6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides, acetoacetanilide, arylamine, molecular iodine",
author = "Gein, {V. L.} and Yankin, {A. N.} and Nosova, {N. V.} and Dmitriev, {M. V.} and Nasakin, {O. E.}",
year = "2016",
month = jan,
day = "1",
doi = "10.1134/S1070363216010114",
language = "English",
volume = "86",
pages = "58--61",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "1",

}

RIS

TY - JOUR

T1 - Formation of 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine

AU - Gein, V. L.

AU - Yankin, A. N.

AU - Nosova, N. V.

AU - Dmitriev, M. V.

AU - Nasakin, O. E.

PY - 2016/1/1

Y1 - 2016/1/1

N2 - Reactions of acetoacetanilide with aromatic aldehydes in ethanol at room temperature in the presence of molecular iodine and arylamine afford to 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides. The structure of obtained compounds was confirmed by mass spectrometry, IR and NMR spectroscopy data.

AB - Reactions of acetoacetanilide with aromatic aldehydes in ethanol at room temperature in the presence of molecular iodine and arylamine afford to 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides. The structure of obtained compounds was confirmed by mass spectrometry, IR and NMR spectroscopy data.

KW - 6-aryl-2-methyl-4-oxo-N,N'-diphenyl-2-cyclohexene-1,3-dicarboxamides

KW - acetoacetanilide

KW - arylamine

KW - molecular iodine

UR - http://www.scopus.com/inward/record.url?scp=84959489365&partnerID=8YFLogxK

U2 - 10.1134/S1070363216010114

DO - 10.1134/S1070363216010114

M3 - Article

AN - SCOPUS:84959489365

VL - 86

SP - 58

EP - 61

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 1

ER -

ID: 36325900