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Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups. / Anisimova, N. A.; Slobodchikova, E. K.; Berestovitskaya, V. M. и др.

в: Russian Journal of General Chemistry, Том 88, № 5, 01.05.2018, стр. 883-891.

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

Harvard

Anisimova, NA, Slobodchikova, EK, Berestovitskaya, VM, Ivanova, ME, Kuzhaeva, AA & Rybalova, TV 2018, 'Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups', Russian Journal of General Chemistry, Том. 88, № 5, стр. 883-891. https://doi.org/10.1134/S1070363218050079

APA

Anisimova, N. A., Slobodchikova, E. K., Berestovitskaya, V. M., Ivanova, M. E., Kuzhaeva, A. A., & Rybalova, T. V. (2018). Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups. Russian Journal of General Chemistry, 88(5), 883-891. https://doi.org/10.1134/S1070363218050079

Vancouver

Anisimova NA, Slobodchikova EK, Berestovitskaya VM, Ivanova ME, Kuzhaeva AA, Rybalova TV. Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups. Russian Journal of General Chemistry. 2018 май 1;88(5):883-891. doi: 10.1134/S1070363218050079

Author

Anisimova, N. A. ; Slobodchikova, E. K. ; Berestovitskaya, V. M. и др. / Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups. в: Russian Journal of General Chemistry. 2018 ; Том 88, № 5. стр. 883-891.

BibTeX

@article{b971f10ea09449b1b5ba8e09e62e8ce4,
title = "Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups",
abstract = "Cyclohexenes functionalized by nitro and trihalomethyl groups were produced by condensation of 1-nitro- and 1-bromo-1-nitro-3,3,3-trifluoro(chloro)propenes with 2-methyl- and 2,3-dimethyl-1,3-butadienes; their structure was characterized by IR, 1H, 13C, 19F NMR spectroscopy, and X-ray diffraction method.",
keywords = "1-nitro-3,3,3-trifluoro(chloro)propenes, acyclic dienes, cyclohexenes, Diels–Alder reaction, trihalomethyl group, DIELS-ALDER REACTIONS, CRYSTAL-STRUCTURES, PHOSPHORYLATED NITROCYCLOHEXENES, PACLITAXEL, DATABASE, (+/-)-EPIBATIDINE, A-RING, Diels-Alder reaction, INHIBITOR, DERIVATIVES",
author = "Anisimova, {N. A.} and Slobodchikova, {E. K.} and Berestovitskaya, {V. M.} and Ivanova, {M. E.} and Kuzhaeva, {A. A.} and Rybalova, {T. V.}",
year = "2018",
month = may,
day = "1",
doi = "10.1134/S1070363218050079",
language = "English",
volume = "88",
pages = "883--891",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "5",

}

RIS

TY - JOUR

T1 - Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups

AU - Anisimova, N. A.

AU - Slobodchikova, E. K.

AU - Berestovitskaya, V. M.

AU - Ivanova, M. E.

AU - Kuzhaeva, A. A.

AU - Rybalova, T. V.

PY - 2018/5/1

Y1 - 2018/5/1

N2 - Cyclohexenes functionalized by nitro and trihalomethyl groups were produced by condensation of 1-nitro- and 1-bromo-1-nitro-3,3,3-trifluoro(chloro)propenes with 2-methyl- and 2,3-dimethyl-1,3-butadienes; their structure was characterized by IR, 1H, 13C, 19F NMR spectroscopy, and X-ray diffraction method.

AB - Cyclohexenes functionalized by nitro and trihalomethyl groups were produced by condensation of 1-nitro- and 1-bromo-1-nitro-3,3,3-trifluoro(chloro)propenes with 2-methyl- and 2,3-dimethyl-1,3-butadienes; their structure was characterized by IR, 1H, 13C, 19F NMR spectroscopy, and X-ray diffraction method.

KW - 1-nitro-3,3,3-trifluoro(chloro)propenes

KW - acyclic dienes

KW - cyclohexenes

KW - Diels–Alder reaction

KW - trihalomethyl group

KW - DIELS-ALDER REACTIONS

KW - CRYSTAL-STRUCTURES

KW - PHOSPHORYLATED NITROCYCLOHEXENES

KW - PACLITAXEL

KW - DATABASE

KW - (+/-)-EPIBATIDINE

KW - A-RING

KW - Diels-Alder reaction

KW - INHIBITOR

KW - DERIVATIVES

UR - http://www.scopus.com/inward/record.url?scp=85049324988&partnerID=8YFLogxK

U2 - 10.1134/S1070363218050079

DO - 10.1134/S1070363218050079

M3 - Article

AN - SCOPUS:85049324988

VL - 88

SP - 883

EP - 891

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 5

ER -

ID: 14317788