Transformations of 5-Hydrazinyl-1,2,4-triazines in Reaction with 2,5-Norbornadiene

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Transformations of 5-Hydrazinyl-1,2,4-triazines in Reaction with 2,5-Norbornadiene. / Krinochkin, A. P.; Rammohan, A.; Kopchuk, D. S. et al.
In: Doklady Chemistry, Vol. 508, No. 1, 01.01.2023, p. 23-27.

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

BibTeX

@article{9beff100f8e140d0bd4da0ae3d87f3ae,

title = "Transformations of 5-Hydrazinyl-1,2,4-triazines in Reaction with 2,5-Norbornadiene",

abstract = "Reaction of 5-hydrazinyl-substituted 1,2,4-triazines and 2,5-norbornadiene at elevated pressure and temperature (in autoclave) has been studied; the reaction yields 2-aminopyridines, 5-amino-1,2,4,-triazines, and 6-unsubstituted pyridines (formation of one of two latter products is dependent on the nature of substituent in the C3 position of triazine).",

author = "Krinochkin, {A. P.} and A. Rammohan and Kopchuk, {D. S.} and Nikonov, {I. L.} and Starnovskaya, {E. S.} and Sharafieva, {E. R.} and Kovalev, {I. S.} and Zyryanov, {G. V.} and Chupakhin, {O. N.}",

note = "Текст о финансировании #1 This work was supported by the Council for grants of the President of the Russian Federation (project no. NSh–1223.2022.1.3), and the State assignment no. АААА-А19-119011790132-7. Текст о финансировании #2 The authors thank M.I. Kodess and the staff of the Laboratory of NMR spectroscopy, as well as the Group of Elemental Analysis, Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences (Yekaterinburg) for the study of the prepared compounds.",

year = "2023",

month = jan,

day = "1",

doi = "10.1134/S0012500823600104",

language = "English",

volume = "508",

pages = "23--27",

journal = "Doklady Chemistry",

issn = "0012-5008",

publisher = "Maik Nauka-Interperiodica Publishing",

number = "1",

}

RIS

TY - JOUR

T1 - Transformations of 5-Hydrazinyl-1,2,4-triazines in Reaction with 2,5-Norbornadiene

AU - Krinochkin, A. P.

AU - Rammohan, A.

AU - Kopchuk, D. S.

AU - Nikonov, I. L.

AU - Starnovskaya, E. S.

AU - Sharafieva, E. R.

AU - Kovalev, I. S.

AU - Zyryanov, G. V.

AU - Chupakhin, O. N.

N1 - Текст о финансировании #1 This work was supported by the Council for grants of the President of the Russian Federation (project no. NSh–1223.2022.1.3), and the State assignment no. АААА-А19-119011790132-7. Текст о финансировании #2 The authors thank M.I. Kodess and the staff of the Laboratory of NMR spectroscopy, as well as the Group of Elemental Analysis, Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences (Yekaterinburg) for the study of the prepared compounds.

PY - 2023/1/1

Y1 - 2023/1/1

N2 - Reaction of 5-hydrazinyl-substituted 1,2,4-triazines and 2,5-norbornadiene at elevated pressure and temperature (in autoclave) has been studied; the reaction yields 2-aminopyridines, 5-amino-1,2,4,-triazines, and 6-unsubstituted pyridines (formation of one of two latter products is dependent on the nature of substituent in the C3 position of triazine).

AB - Reaction of 5-hydrazinyl-substituted 1,2,4-triazines and 2,5-norbornadiene at elevated pressure and temperature (in autoclave) has been studied; the reaction yields 2-aminopyridines, 5-amino-1,2,4,-triazines, and 6-unsubstituted pyridines (formation of one of two latter products is dependent on the nature of substituent in the C3 position of triazine).

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000994243700004

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85160108150

U2 - 10.1134/S0012500823600104

DO - 10.1134/S0012500823600104

M3 - Article

VL - 508

SP - 23

EP - 27

JO - Doklady Chemistry

JF - Doklady Chemistry

SN - 0012-5008

IS - 1

ER -

ID: 40049590