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Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines. / Krinochkin, A.; Rammohan, A.; Shtaitz, Ya. et al.
In: Doklady Chemistry, Vol. 508, No. 1, 01.01.2023, p. 28-31.

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

Harvard

Krinochkin, A, Rammohan, A, Shtaitz, Y, Kopchuk, D, Ladin, E, Sharafieva, E, Taniya, O, Zyryanov, G, Matern, A & Chupakhin, O 2023, 'Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines', Doklady Chemistry, vol. 508, no. 1, pp. 28-31. https://doi.org/10.1134/S0012500823600153

APA

Krinochkin, A., Rammohan, A., Shtaitz, Y., Kopchuk, D., Ladin, E., Sharafieva, E., Taniya, O., Zyryanov, G., Matern, A., & Chupakhin, O. (2023). Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines. Doklady Chemistry, 508(1), 28-31. https://doi.org/10.1134/S0012500823600153

Vancouver

Krinochkin A, Rammohan A, Shtaitz Y, Kopchuk D, Ladin E, Sharafieva E et al. Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines. Doklady Chemistry. 2023 Jan 1;508(1):28-31. doi: 10.1134/S0012500823600153

Author

Krinochkin, A. ; Rammohan, A. ; Shtaitz, Ya. et al. / Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines. In: Doklady Chemistry. 2023 ; Vol. 508, No. 1. pp. 28-31.

BibTeX

@article{36a6282d472c4c3ab70e9faa46d07e92,
title = "Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines",
abstract = "An interaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2‑amino-4-aryl-substituted thiazoles and oxazoles has been studied. The difference in the reactivity of these aminoheterocycles depending on the presence of an oxygen or a sulfur atom in their composition has been demonstrated. Previously, the 4-aryl-3-hydroxy-2,2′-bipyridines were obtained as products of aza-Diels−Alder reaction between 6-aryl-3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles and 2-amino-4-aryloxazoles. It was shown that the reaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2-aminothiazoles led to the products of ipso-substitution of cyano group. The aza-Diels−Alder reaction of these compounds with 2,5-norbornadiene gave (2,2′-bi)pyridines with the 2-aminothiazolyl at alpha-position.",
author = "A. Krinochkin and A. Rammohan and Ya. Shtaitz and D. Kopchuk and E. Ladin and E. Sharafieva and O. Taniya and G. Zyryanov and A. Matern and O. Chupakhin",
note = "This work was supported by the Council for Grants of the President of the Russian Federation (Grant no. MK-320.2021.1.3).",
year = "2023",
month = jan,
day = "1",
doi = "10.1134/S0012500823600153",
language = "English",
volume = "508",
pages = "28--31",
journal = "Doklady Chemistry",
issn = "0012-5008",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "1",

}

RIS

TY - JOUR

T1 - Interaction of 2-Amino-(4-aryl)-Substituted Thia- and Oxazoles with 5-Cyano-1,2,4-triazines

AU - Krinochkin, A.

AU - Rammohan, A.

AU - Shtaitz, Ya.

AU - Kopchuk, D.

AU - Ladin, E.

AU - Sharafieva, E.

AU - Taniya, O.

AU - Zyryanov, G.

AU - Matern, A.

AU - Chupakhin, O.

N1 - This work was supported by the Council for Grants of the President of the Russian Federation (Grant no. MK-320.2021.1.3).

PY - 2023/1/1

Y1 - 2023/1/1

N2 - An interaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2‑amino-4-aryl-substituted thiazoles and oxazoles has been studied. The difference in the reactivity of these aminoheterocycles depending on the presence of an oxygen or a sulfur atom in their composition has been demonstrated. Previously, the 4-aryl-3-hydroxy-2,2′-bipyridines were obtained as products of aza-Diels−Alder reaction between 6-aryl-3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles and 2-amino-4-aryloxazoles. It was shown that the reaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2-aminothiazoles led to the products of ipso-substitution of cyano group. The aza-Diels−Alder reaction of these compounds with 2,5-norbornadiene gave (2,2′-bi)pyridines with the 2-aminothiazolyl at alpha-position.

AB - An interaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2‑amino-4-aryl-substituted thiazoles and oxazoles has been studied. The difference in the reactivity of these aminoheterocycles depending on the presence of an oxygen or a sulfur atom in their composition has been demonstrated. Previously, the 4-aryl-3-hydroxy-2,2′-bipyridines were obtained as products of aza-Diels−Alder reaction between 6-aryl-3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles and 2-amino-4-aryloxazoles. It was shown that the reaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2-aminothiazoles led to the products of ipso-substitution of cyano group. The aza-Diels−Alder reaction of these compounds with 2,5-norbornadiene gave (2,2′-bi)pyridines with the 2-aminothiazolyl at alpha-position.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000994243700005

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85160030930

U2 - 10.1134/S0012500823600153

DO - 10.1134/S0012500823600153

M3 - Article

VL - 508

SP - 28

EP - 31

JO - Doklady Chemistry

JF - Doklady Chemistry

SN - 0012-5008

IS - 1

ER -

ID: 40049893