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Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions. / Sadchikova, E. V.; Mokrushin, V. S.
в: Russian Chemical Bulletin, Том 54, № 2, 01.02.2005, стр. 354-365.

Результаты исследований: Вклад в журнал › Статья › Рецензирование

Harvard

Sadchikova, EV & Mokrushin, VS 2005, 'Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions', Russian Chemical Bulletin, Том. 54, № 2, стр. 354-365. https://doi.org/10.1007/s11172-005-0259-7

APA

Sadchikova, E. V., & Mokrushin, V. S. (2005). Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions. Russian Chemical Bulletin, 54(2), 354-365. https://doi.org/10.1007/s11172-005-0259-7

Vancouver

Sadchikova EV, Mokrushin VS. Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions. Russian Chemical Bulletin. 2005 февр. 1;54(2):354-365. doi: 10.1007/s11172-005-0259-7

Author

Sadchikova, E. V. ; Mokrushin, V. S. / Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions. в: Russian Chemical Bulletin. 2005 ; Том 54, № 2. стр. 354-365.

BibTeX

@article{6d288e463e544f6390045503b384b166,
title = "Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions",
abstract = "The comparative reactivity of heterocyclic diazo compounds and the corresponding diazonium salts in C-azo coupling reactions was studied using imidazole, pyrazole, and triazole derivatives as examples.The reactivities of pyrazole- and imidazole-derived diazonium salts are much lower than those of thiadiazole- and 1,2,4-triazole-derived diazonium salts but higher than those of pyrrole and indole diazo compounds.",
author = "Sadchikova, {E. V.} and Mokrushin, {V. S.}",
note = "This work was financially supported by the Russian Foundation for Basic Research (Project No. 04 03 96121a).",
year = "2005",
month = feb,
day = "1",
doi = "10.1007/s11172-005-0259-7",
language = "English",
volume = "54",
pages = "354--365",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "2",

}

RIS

TY - JOUR

T1 - Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions

AU - Sadchikova, E. V.

AU - Mokrushin, V. S.

N1 - This work was financially supported by the Russian Foundation for Basic Research (Project No. 04 03 96121a).

PY - 2005/2/1

Y1 - 2005/2/1

N2 - The comparative reactivity of heterocyclic diazo compounds and the corresponding diazonium salts in C-azo coupling reactions was studied using imidazole, pyrazole, and triazole derivatives as examples.The reactivities of pyrazole- and imidazole-derived diazonium salts are much lower than those of thiadiazole- and 1,2,4-triazole-derived diazonium salts but higher than those of pyrrole and indole diazo compounds.

AB - The comparative reactivity of heterocyclic diazo compounds and the corresponding diazonium salts in C-azo coupling reactions was studied using imidazole, pyrazole, and triazole derivatives as examples.The reactivities of pyrazole- and imidazole-derived diazonium salts are much lower than those of thiadiazole- and 1,2,4-triazole-derived diazonium salts but higher than those of pyrrole and indole diazo compounds.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000231336600010

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=25444472096

U2 - 10.1007/s11172-005-0259-7

DO - 10.1007/s11172-005-0259-7

M3 - Article

VL - 54

SP - 354

EP - 365

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 2

ER -

ID: 41351117