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Synthesis of fully-substituted pyridines and dihydropyridines in a highly chemoselective manner utilizing a multicomponent reaction (MCR) strategy
Тип публикации: Journal Article
Дата публикации: 2014-10-24
scimago Q1
wos Q2
БС1
SJR: 0.777
CiteScore: 7.6
Impact factor: 4.6
ISSN: 20462069
General Chemistry
General Chemical Engineering
Краткое описание
An efficient protocol has been developed for the synthesis of pyridines and 1,4-dihydropyridines based on chemoselective multicomponent reactions.
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ГОСТ
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Sarkar S., Das D. K., KHAN A. N. Synthesis of fully-substituted pyridines and dihydropyridines in a highly chemoselective manner utilizing a multicomponent reaction (MCR) strategy // RSC Advances. 2014. Vol. 4. No. 96. pp. 53752-53760.
ГОСТ со всеми авторами (до 50)
Скопировать
Sarkar S., Das D. K., KHAN A. N. Synthesis of fully-substituted pyridines and dihydropyridines in a highly chemoselective manner utilizing a multicomponent reaction (MCR) strategy // RSC Advances. 2014. Vol. 4. No. 96. pp. 53752-53760.
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RIS
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TY - JOUR
DO - 10.1039/c4ra08237k
UR - https://doi.org/10.1039/c4ra08237k
TI - Synthesis of fully-substituted pyridines and dihydropyridines in a highly chemoselective manner utilizing a multicomponent reaction (MCR) strategy
T2 - RSC Advances
AU - Sarkar, Satavisha
AU - Das, Deb K.
AU - KHAN, ABU N.G.A.
PY - 2014
DA - 2014/10/24
PB - Royal Society of Chemistry (RSC)
SP - 53752-53760
IS - 96
VL - 4
SN - 2046-2069
ER -
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BibTex (до 50 авторов)
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@article{2014_Sarkar,
author = {Satavisha Sarkar and Deb K. Das and ABU N.G.A. KHAN},
title = {Synthesis of fully-substituted pyridines and dihydropyridines in a highly chemoselective manner utilizing a multicomponent reaction (MCR) strategy},
journal = {RSC Advances},
year = {2014},
volume = {4},
publisher = {Royal Society of Chemistry (RSC)},
month = {oct},
url = {https://doi.org/10.1039/c4ra08237k},
number = {96},
pages = {53752--53760},
doi = {10.1039/c4ra08237k}
}
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MLA
Скопировать
Sarkar, Satavisha, et al. “Synthesis of fully-substituted pyridines and dihydropyridines in a highly chemoselective manner utilizing a multicomponent reaction (MCR) strategy.” RSC Advances, vol. 4, no. 96, Oct. 2014, pp. 53752-53760. https://doi.org/10.1039/c4ra08237k.