Electrocatalytic multicomponent assembling of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile: facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system
Publication type: Journal Article
Publication date: 2008-12-02
scimago Q2
wos Q2
SJR: 0.646
CiteScore: 8.5
Impact factor: 3.8
ISSN: 13811991, 1573501X
PubMed ID:
19048382
Catalysis
Organic Chemistry
Drug Discovery
Inorganic Chemistry
Physical and Theoretical Chemistry
Molecular Biology
General Medicine
Information Systems
Abstract
Electrochemically induced catalytic multicomponent transformation of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile in ethanol in an undivided cell in the presence of sodium bromide as an electrolyte results in the formation of spirooxindoles with fused functionalized pyrano[2,3-c]pyrazole system in 78–99} yields. The developed efficient electrocatalytic approach to medicinally relevant spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazoles] is beneficial from the viewpoint of diversity-oriented large-scale processes and represents a novel example of facile environmentally benign synthetic concept for electrocatalytic multicomponent reaction strategy.
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Total citations:
61
Citations from 2025:
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(4.92%)
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Elinson M. N. et al. Electrocatalytic multicomponent assembling of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile: facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system // Molecular Diversity. 2008. Vol. 13. No. 1. pp. 47-52.
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Elinson M. N., Dorofeev A. S., Miloserdov F. M., Nikishin G. I. Electrocatalytic multicomponent assembling of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile: facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system // Molecular Diversity. 2008. Vol. 13. No. 1. pp. 47-52.
Cite this
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TY - JOUR
DO - 10.1007/s11030-008-9100-1
UR - https://doi.org/10.1007/s11030-008-9100-1
TI - Electrocatalytic multicomponent assembling of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile: facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system
T2 - Molecular Diversity
AU - Elinson, Michail N
AU - Dorofeev, Alexander S.
AU - Miloserdov, Fedor M
AU - Nikishin, Gennady I.
PY - 2008
DA - 2008/12/02
PB - Springer Nature
SP - 47-52
IS - 1
VL - 13
PMID - 19048382
SN - 1381-1991
SN - 1573-501X
ER -
Cite this
BibTex (up to 50 authors)
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@article{2008_Elinson,
author = {Michail N Elinson and Alexander S. Dorofeev and Fedor M Miloserdov and Gennady I. Nikishin},
title = {Electrocatalytic multicomponent assembling of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile: facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system},
journal = {Molecular Diversity},
year = {2008},
volume = {13},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007/s11030-008-9100-1},
number = {1},
pages = {47--52},
doi = {10.1007/s11030-008-9100-1}
}
Cite this
MLA
Copy
Elinson, Michail N., et al. “Electrocatalytic multicomponent assembling of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile: facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system.” Molecular Diversity, vol. 13, no. 1, Dec. 2008, pp. 47-52. https://doi.org/10.1007/s11030-008-9100-1.