том 22 издание 1 страницы 37-38

Reactions of quinoxaline with 3-methyl-1-phenylpyrazol-5-one

Тип публикацииJournal Article
Дата публикации2012-01-31
scimago Q3
wos Q3
БС1
SJR0.305
CiteScore3
Impact factor1.7
ISSN09599436, 1364551X
General Chemistry
Краткое описание
Quinoxaline during the reaction with 3-methyl-1-phenylpyrazol-5-one in the presence of triethylamine at room temperature in dimethylsulfoxide eliminates o-phenylenediamine and gives 4,4’-methylene-bis(3-methyl-1-phenylpyrazol-5-one) and 1,1,2,2-tetrakis(5-methyl-2-oxo-2-phenyl-1,2-dihydro-3H-pyrazol-4-yl)ethane. The latter was proved to be the intermediate to form the above dipyrazolylmethane derivative.
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ГОСТ |
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Azev Y. A. et al. Reactions of quinoxaline with 3-methyl-1-phenylpyrazol-5-one // Mendeleev Communications. 2012. Vol. 22. No. 1. pp. 37-38.
ГОСТ со всеми авторами (до 50) Скопировать
Azev Y. A., Oparina E. D., Kovalev I., Slepukhin P. A., Novikova R. K. Reactions of quinoxaline with 3-methyl-1-phenylpyrazol-5-one // Mendeleev Communications. 2012. Vol. 22. No. 1. pp. 37-38.
RIS |
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TY - JOUR
DO - 10.1016/j.mencom.2012.01.014
UR - https://doi.org/10.1016/j.mencom.2012.01.014
TI - Reactions of quinoxaline with 3-methyl-1-phenylpyrazol-5-one
T2 - Mendeleev Communications
AU - Azev, Yurii A.
AU - Oparina, Elena D
AU - Kovalev, Igor
AU - Slepukhin, Pavel A.
AU - Novikova, Rashida K
PY - 2012
DA - 2012/01/31
PB - OOO Zhurnal "Mendeleevskie Soobshcheniya"
SP - 37-38
IS - 1
VL - 22
SN - 0959-9436
SN - 1364-551X
ER -
BibTex |
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@article{2012_Azev,
author = {Yurii A. Azev and Elena D Oparina and Igor Kovalev and Pavel A. Slepukhin and Rashida K Novikova},
title = {Reactions of quinoxaline with 3-methyl-1-phenylpyrazol-5-one},
journal = {Mendeleev Communications},
year = {2012},
volume = {22},
publisher = {OOO Zhurnal "Mendeleevskie Soobshcheniya"},
month = {jan},
url = {https://doi.org/10.1016/j.mencom.2012.01.014},
number = {1},
pages = {37--38},
doi = {10.1016/j.mencom.2012.01.014}
}
MLA
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Azev, Yurii A., et al. “Reactions of quinoxaline with 3-methyl-1-phenylpyrazol-5-one.” Mendeleev Communications, vol. 22, no. 1, Jan. 2012, pp. 37-38. https://doi.org/10.1016/j.mencom.2012.01.014.