Mendeleev Communications, volume 25, issue 1, pages 36-38
Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans
Publication type: Journal Article
Publication date: 2015-01-28
Journal:
Mendeleev Communications
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.9
ISSN: 09599436, 1364551X
General Chemistry
Abstract
Hetarylthiofuroxans were synthesized by nucleophilic substitution of the nitro group in 4-nitrofuroxans under the action of hetarylthiols in the DBU–MeCN system at room temperature, reactivity of 4-nitrofuroxans being dependent on the C(3)-substituent.
Citations by journals
1
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Bulletin of the Korean Chemical Society
1 publication, 3.57%
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ChemistrySelect
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1 publication, 3.57%
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1 publication, 3.57%
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Molecules
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1 publication, 3.57%
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1
2
3
4
5
6
7
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Citations by publishers
2
4
6
8
10
12
14
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Elsevier
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13 publications, 46.43%
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Springer Nature
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Springer Nature
6 publications, 21.43%
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Royal Society of Chemistry (RSC)
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3 publications, 10.71%
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Wiley
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Wiley
3 publications, 10.71%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 publications, 7.14%
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Multidisciplinary Digital Publishing Institute (MDPI)
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Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 3.57%
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2
4
6
8
10
12
14
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Fershtat L. L. et al. Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans // Mendeleev Communications. 2015. Vol. 25. No. 1. pp. 36-38.
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Fershtat L. L., Epishina M. A., Kulikov A., Makhova N. N. Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans // Mendeleev Communications. 2015. Vol. 25. No. 1. pp. 36-38.
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TY - JOUR
DO - 10.1016/j.mencom.2015.01.013
UR - https://doi.org/10.1016%2Fj.mencom.2015.01.013
TI - Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans
T2 - Mendeleev Communications
AU - Epishina, Margarita A.
AU - Fershtat, Leonid L.
AU - Kulikov, Alexander
AU - Makhova, Nina N.
PY - 2015
DA - 2015/01/28 00:00:00
PB - Elsevier
SP - 36-38
IS - 1
VL - 25
SN - 0959-9436
SN - 1364-551X
ER -
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@article{2015_Fershtat,
author = {Margarita A. Epishina and Leonid L. Fershtat and Alexander Kulikov and Nina N. Makhova},
title = {Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016%2Fj.mencom.2015.01.013},
number = {1},
pages = {36--38},
doi = {10.1016/j.mencom.2015.01.013}
}
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MLA
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Fershtat, Leonid L., et al. “Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans.” Mendeleev Communications, vol. 25, no. 1, Jan. 2015, pp. 36-38. https://doi.org/10.1016%2Fj.mencom.2015.01.013.