том 12 издание 48 страницы 9786-9788

Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones

Тип публикацииJournal Article
Дата публикации2014-10-30
scimago Q2
wos Q2
БС1
SJR0.600
CiteScore5.2
Impact factor2.7
ISSN14770520, 14770539
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
A modular approach to 3-substituted 2-quinolones via a cascade annulation reaction between 4-nitroketones and hydrazines has been developed.
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ГОСТ |
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Aksenov A. et al. Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones // Organic and Biomolecular Chemistry. 2014. Vol. 12. No. 48. pp. 9786-9788.
ГОСТ со всеми авторами (до 50) Скопировать
Aksenov A., Smirnov A., Aksenov N. A., Aksenova I. V., Bijieva A. S., Rubin M. Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones // Organic and Biomolecular Chemistry. 2014. Vol. 12. No. 48. pp. 9786-9788.
RIS |
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TY - JOUR
DO - 10.1039/C4OB02131B
UR - https://doi.org/10.1039/C4OB02131B
TI - Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones
T2 - Organic and Biomolecular Chemistry
AU - Aksenov, Alexander
AU - Smirnov, A.V.
AU - Aksenov, Nicolai A.
AU - Aksenova, Inna V.
AU - Bijieva, Asiyat S
AU - Rubin, Michael
PY - 2014
DA - 2014/10/30
PB - Royal Society of Chemistry (RSC)
SP - 9786-9788
IS - 48
VL - 12
PMID - 25371015
SN - 1477-0520
SN - 1477-0539
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2014_Aksenov,
author = {Alexander Aksenov and A.V. Smirnov and Nicolai A. Aksenov and Inna V. Aksenova and Asiyat S Bijieva and Michael Rubin},
title = {Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones},
journal = {Organic and Biomolecular Chemistry},
year = {2014},
volume = {12},
publisher = {Royal Society of Chemistry (RSC)},
month = {oct},
url = {https://doi.org/10.1039/C4OB02131B},
number = {48},
pages = {9786--9788},
doi = {10.1039/C4OB02131B}
}
MLA
Цитировать
Aksenov, Alexander, et al. “Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones.” Organic and Biomolecular Chemistry, vol. 12, no. 48, Oct. 2014, pp. 9786-9788. https://doi.org/10.1039/C4OB02131B.