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Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium. / Rammohan, A.; Krinochkin, A.; Kopchuk, D. et al.
In: Russian Journal of Organic Chemistry, Vol. 59, No. 9, 2023, p. 1633-1636.

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

Harvard

Rammohan, A, Krinochkin, A, Kopchuk, D, Shtaitz, Y, Sharafieva, E, Gaviko, V, Zyryanov, G & Chupakhin, O 2023, 'Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium', Russian Journal of Organic Chemistry, vol. 59, no. 9, pp. 1633-1636. https://doi.org/10.1134/S1070428023090233

APA

Rammohan, A., Krinochkin, A., Kopchuk, D., Shtaitz, Y., Sharafieva, E., Gaviko, V., Zyryanov, G., & Chupakhin, O. (2023). Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium. Russian Journal of Organic Chemistry, 59(9), 1633-1636. https://doi.org/10.1134/S1070428023090233

Vancouver

Rammohan A, Krinochkin A, Kopchuk D, Shtaitz Y, Sharafieva E, Gaviko V et al. Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium. Russian Journal of Organic Chemistry. 2023;59(9):1633-1636. doi: 10.1134/S1070428023090233

Author

Rammohan, A. ; Krinochkin, A. ; Kopchuk, D. et al. / Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium. In: Russian Journal of Organic Chemistry. 2023 ; Vol. 59, No. 9. pp. 1633-1636.

BibTeX

@article{e4959ef0542341a88e8e4de96bec23d8,
title = "Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium",
abstract = "We previously reported the solvent-free reaction of 5-aryl-3-(pyridin-2-yl)-1,2,4-triazine-5-carbo­nitriles with 2-amino-4-aryl-1,3-oxazoles, which afforded 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles. Similar reaction in anhydrous medium led to the formation of two products, previously described 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles (up to 44%) and 4,5-diaryl-2,2′-bipyridine-6-carbonitriles (up to 32%). {\textcopyright} 2023, The Author(s).",
author = "A. Rammohan and A. Krinochkin and D. Kopchuk and Ya. Shtaitz and E. Sharafieva and V. Gaviko and G. Zyryanov and O. Chupakhin",
note = "This study was financially supported by the Council for Grants at the President of the Russian Federation (project no. MK-320.2021.1.3)",
year = "2023",
doi = "10.1134/S1070428023090233",
language = "English",
volume = "59",
pages = "1633--1636",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "9",

}

RIS

TY - JOUR

T1 - Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium

AU - Rammohan, A.

AU - Krinochkin, A.

AU - Kopchuk, D.

AU - Shtaitz, Ya.

AU - Sharafieva, E.

AU - Gaviko, V.

AU - Zyryanov, G.

AU - Chupakhin, O.

N1 - This study was financially supported by the Council for Grants at the President of the Russian Federation (project no. MK-320.2021.1.3)

PY - 2023

Y1 - 2023

N2 - We previously reported the solvent-free reaction of 5-aryl-3-(pyridin-2-yl)-1,2,4-triazine-5-carbo­nitriles with 2-amino-4-aryl-1,3-oxazoles, which afforded 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles. Similar reaction in anhydrous medium led to the formation of two products, previously described 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles (up to 44%) and 4,5-diaryl-2,2′-bipyridine-6-carbonitriles (up to 32%). © 2023, The Author(s).

AB - We previously reported the solvent-free reaction of 5-aryl-3-(pyridin-2-yl)-1,2,4-triazine-5-carbo­nitriles with 2-amino-4-aryl-1,3-oxazoles, which afforded 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles. Similar reaction in anhydrous medium led to the formation of two products, previously described 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles (up to 44%) and 4,5-diaryl-2,2′-bipyridine-6-carbonitriles (up to 32%). © 2023, The Author(s).

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85177430543

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=001156603300006

U2 - 10.1134/S1070428023090233

DO - 10.1134/S1070428023090233

M3 - Article

VL - 59

SP - 1633

EP - 1636

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 9

ER -

ID: 49311028