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Результаты исследований: Вклад в журнал › Статья › Рецензирование
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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