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Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts. / Sadchikova, E. V.; Mokrushin, V. S.
In: Russian Chemical Bulletin, Vol. 52, No. 7, 01.01.2003, p. 1600-1605.

Research output: Contribution to journal › Article › peer-review

Harvard

Sadchikova, EV & Mokrushin, VS 2003, 'Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts', Russian Chemical Bulletin, vol. 52, no. 7, pp. 1600-1605. https://doi.org/10.1023/A:1025605512301

APA

Sadchikova, E. V., & Mokrushin, V. S. (2003). Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts. Russian Chemical Bulletin, 52(7), 1600-1605. https://doi.org/10.1023/A:1025605512301

Vancouver

Sadchikova EV, Mokrushin VS. Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts. Russian Chemical Bulletin. 2003 Jan 1;52(7):1600-1605. doi: 10.1023/A:1025605512301

Author

Sadchikova, E. V. ; Mokrushin, V. S. / Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts. In: Russian Chemical Bulletin. 2003 ; Vol. 52, No. 7. pp. 1600-1605.

BibTeX

@article{10c6058e091142bb8c81c7e83d10a88c,
title = "Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts",
abstract = "Diazotization of 4-R-5-aminoimidazoles (R = CONHAr, CONHAIk, morpholinocarbonyl, or piperidinocarbonyl) with sodium nitrite in aqueous solutions of mineral acids afforded the corresponding 5-diazoimidazoles, whereas the reactions in concentrated tetrafluoroboric acid produced imidazolyl-5-diazonium salts. In the solid phase, diazonium salts are transformed into the corresponding diazo compounds.",
author = "Sadchikova, {E. V.} and Mokrushin, {V. S.}",
note = "This study was financially supported by the Russian Foundation for Basic Research (Project No. 01 03 96433a) and the US Civilian Research and Development Foundation (Grants RC1 2393 EK 02 and REC 005).",
year = "2003",
month = jan,
day = "1",
doi = "10.1023/A:1025605512301",
language = "English",
volume = "52",
pages = "1600--1605",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "7",

}

RIS

TY - JOUR

T1 - Synthesis and properties of 5-diazoimidazoles and imidazolyl-5-diazonium salts

AU - Sadchikova, E. V.

AU - Mokrushin, V. S.

N1 - This study was financially supported by the Russian Foundation for Basic Research (Project No. 01 03 96433a) and the US Civilian Research and Development Foundation (Grants RC1 2393 EK 02 and REC 005).

PY - 2003/1/1

Y1 - 2003/1/1

N2 - Diazotization of 4-R-5-aminoimidazoles (R = CONHAr, CONHAIk, morpholinocarbonyl, or piperidinocarbonyl) with sodium nitrite in aqueous solutions of mineral acids afforded the corresponding 5-diazoimidazoles, whereas the reactions in concentrated tetrafluoroboric acid produced imidazolyl-5-diazonium salts. In the solid phase, diazonium salts are transformed into the corresponding diazo compounds.

AB - Diazotization of 4-R-5-aminoimidazoles (R = CONHAr, CONHAIk, morpholinocarbonyl, or piperidinocarbonyl) with sodium nitrite in aqueous solutions of mineral acids afforded the corresponding 5-diazoimidazoles, whereas the reactions in concentrated tetrafluoroboric acid produced imidazolyl-5-diazonium salts. In the solid phase, diazonium salts are transformed into the corresponding diazo compounds.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000185987400022

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=1642450684

U2 - 10.1023/A:1025605512301

DO - 10.1023/A:1025605512301

M3 - Article

VL - 52

SP - 1600

EP - 1605

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 7

ER -

ID: 44163899