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Hydroarylation of (E)-5-(2-Arylethenyl)-2-methyl-2 H -tetrazoles under Superelectrophilic Activation. / Lisakova, Anna D.; Ryabukhin, Dmitry S.; Trifonov, Rostislav E.; Ostrovskii, Vladimir A.; Boyarskaya, Irina A.; Vasilyev, Aleksander V.

в: Synthesis (Germany), Том 49, № 3, ss-2016-n0434-op, 01.02.2017, стр. 579-586.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Lisakova, AD, Ryabukhin, DS, Trifonov, RE, Ostrovskii, VA, Boyarskaya, IA & Vasilyev, AV 2017, 'Hydroarylation of (E)-5-(2-Arylethenyl)-2-methyl-2 H -tetrazoles under Superelectrophilic Activation', Synthesis (Germany), Том. 49, № 3, ss-2016-n0434-op, стр. 579-586. https://doi.org/10.1055/s-0036-1588884

APA

Vancouver

Author

Lisakova, Anna D. ; Ryabukhin, Dmitry S. ; Trifonov, Rostislav E. ; Ostrovskii, Vladimir A. ; Boyarskaya, Irina A. ; Vasilyev, Aleksander V. / Hydroarylation of (E)-5-(2-Arylethenyl)-2-methyl-2 H -tetrazoles under Superelectrophilic Activation. в: Synthesis (Germany). 2017 ; Том 49, № 3. стр. 579-586.

BibTeX

@article{39a28d2624134cc088de97f11dea61ca,
title = "Hydroarylation of (E)-5-(2-Arylethenyl)-2-methyl-2 H -tetrazoles under Superelectrophilic Activation",
abstract = "The reaction of 5-(2-arylethenyl)-2-methyl-2H-tetrazoles with arenes (benzene, xylenes, tert-butylbenzene, anisole, veratrole, 1,2-dichlorobenzene) under conditions of superelectrophilic activation under the action of Bronsted superacids (CF3SO3H, FSO3H) or strong Lewis acids (AlCl3, AlBr3) leads regioselectively to the products of hydroarylation of the carbon-carbon double bond, viz., 5-(2,2-diarylethenyl)-2-methyl-2H-tetazoles, in yields of up to 95%.",
keywords = "Bronsted superacid, Friedel-Crafts reaction, hydroarylation, Lewis superacid, superelectrophilic activation, tetrazoles",
author = "Lisakova, {Anna D.} and Ryabukhin, {Dmitry S.} and Trifonov, {Rostislav E.} and Ostrovskii, {Vladimir A.} and Boyarskaya, {Irina A.} and Vasilyev, {Aleksander V.}",
note = "Publisher Copyright: {\textcopyright} Georg Thieme Verlag Stuttgart · New York-Synthesis 2017.",
year = "2017",
month = feb,
day = "1",
doi = "10.1055/s-0036-1588884",
language = "English",
volume = "49",
pages = "579--586",
journal = "Synthesis",
issn = "0039-7881",
publisher = "Georg Thieme Verlag",
number = "3",

}

RIS

TY - JOUR

T1 - Hydroarylation of (E)-5-(2-Arylethenyl)-2-methyl-2 H -tetrazoles under Superelectrophilic Activation

AU - Lisakova, Anna D.

AU - Ryabukhin, Dmitry S.

AU - Trifonov, Rostislav E.

AU - Ostrovskii, Vladimir A.

AU - Boyarskaya, Irina A.

AU - Vasilyev, Aleksander V.

N1 - Publisher Copyright: © Georg Thieme Verlag Stuttgart · New York-Synthesis 2017.

PY - 2017/2/1

Y1 - 2017/2/1

N2 - The reaction of 5-(2-arylethenyl)-2-methyl-2H-tetrazoles with arenes (benzene, xylenes, tert-butylbenzene, anisole, veratrole, 1,2-dichlorobenzene) under conditions of superelectrophilic activation under the action of Bronsted superacids (CF3SO3H, FSO3H) or strong Lewis acids (AlCl3, AlBr3) leads regioselectively to the products of hydroarylation of the carbon-carbon double bond, viz., 5-(2,2-diarylethenyl)-2-methyl-2H-tetazoles, in yields of up to 95%.

AB - The reaction of 5-(2-arylethenyl)-2-methyl-2H-tetrazoles with arenes (benzene, xylenes, tert-butylbenzene, anisole, veratrole, 1,2-dichlorobenzene) under conditions of superelectrophilic activation under the action of Bronsted superacids (CF3SO3H, FSO3H) or strong Lewis acids (AlCl3, AlBr3) leads regioselectively to the products of hydroarylation of the carbon-carbon double bond, viz., 5-(2,2-diarylethenyl)-2-methyl-2H-tetazoles, in yields of up to 95%.

KW - Bronsted superacid

KW - Friedel-Crafts reaction

KW - hydroarylation

KW - Lewis superacid

KW - superelectrophilic activation

KW - tetrazoles

UR - http://www.scopus.com/inward/record.url?scp=84988661340&partnerID=8YFLogxK

U2 - 10.1055/s-0036-1588884

DO - 10.1055/s-0036-1588884

M3 - Article

AN - SCOPUS:84988661340

VL - 49

SP - 579

EP - 586

JO - Synthesis

JF - Synthesis

SN - 0039-7881

IS - 3

M1 - ss-2016-n0434-op

ER -

ID: 97812675