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Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers. / Korotaev, Vladislav Yu.; Barkov, Alexey Yu.; Ezhikova, Marina A. и др.
в: Chemistry of Heterocyclic Compounds, Том 51, № 6, 06.2015, стр. 531-540.

Результаты исследований: Вклад в журнал › Статья › Рецензирование

Harvard

Korotaev, VY, Barkov, AY, Ezhikova, MA, Kodess, MI & Sosnovskikh, VY 2015, 'Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers', Chemistry of Heterocyclic Compounds, Том. 51, № 6, стр. 531-540. https://doi.org/10.1007/s10593-015-1733-2

APA

Korotaev, V. Y., Barkov, A. Y., Ezhikova, M. A., Kodess, M. I., & Sosnovskikh, V. Y. (2015). Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers. Chemistry of Heterocyclic Compounds, 51(6), 531-540. https://doi.org/10.1007/s10593-015-1733-2

Vancouver

Korotaev VY, Barkov AY, Ezhikova MA, Kodess MI, Sosnovskikh VY. Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers. Chemistry of Heterocyclic Compounds. 2015 июнь;51(6):531-540. doi: 10.1007/s10593-015-1733-2

Author

Korotaev, Vladislav Yu. ; Barkov, Alexey Yu. ; Ezhikova, Marina A. и др. / Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers. в: Chemistry of Heterocyclic Compounds. 2015 ; Том 51, № 6. стр. 531-540.

BibTeX

@article{8a8fe33fd7a34e9da67afba3c1926e7a,
title = "Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers",
keywords = "chromans, 3-nitro-2H-chromenes, push-pull enamines, atropisomerism, nucleophilic addition, POTASSIUM CHANNEL ACTIVATORS, ANTIHYPERTENSIVE ACTIVITY, STEREOSELECTIVE ADDITION, MICHAEL ADDITION, N-NUCLEOPHILES, C-NUCLEOPHILES, S-NUCLEOPHILES, 3-NITRO-2-TRIHALOMETHYL-2H-CHROMENES, 3-NITRO-2H-CHROMENES, ISOMERS",
author = "Korotaev, {Vladislav Yu.} and Barkov, {Alexey Yu.} and Ezhikova, {Marina A.} and Kodess, {Mikhail I.} and Sosnovskikh, {Vyacheslav Ya.}",
year = "2015",
month = jun,
doi = "10.1007/s10593-015-1733-2",
language = "English",
volume = "51",
pages = "531--540",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer Verlag",
number = "6",

}

RIS

TY - JOUR

T1 - Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers

AU - Korotaev, Vladislav Yu.

AU - Barkov, Alexey Yu.

AU - Ezhikova, Marina A.

AU - Kodess, Mikhail I.

AU - Sosnovskikh, Vyacheslav Ya.

PY - 2015/6

Y1 - 2015/6

KW - chromans

KW - 3-nitro-2H-chromenes

KW - push-pull enamines

KW - atropisomerism

KW - nucleophilic addition

KW - POTASSIUM CHANNEL ACTIVATORS

KW - ANTIHYPERTENSIVE ACTIVITY

KW - STEREOSELECTIVE ADDITION

KW - MICHAEL ADDITION

KW - N-NUCLEOPHILES

KW - C-NUCLEOPHILES

KW - S-NUCLEOPHILES

KW - 3-NITRO-2-TRIHALOMETHYL-2H-CHROMENES

KW - 3-NITRO-2H-CHROMENES

KW - ISOMERS

UR - http://www.scopus.com/inward/record.url?scp=84957436943&partnerID=8YFLogxK

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000359431000005

U2 - 10.1007/s10593-015-1733-2

DO - 10.1007/s10593-015-1733-2

M3 - Article

VL - 51

SP - 531

EP - 540

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 6

ER -

ID: 405235