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Electrocatalytic Fast and Efficient Aldol Addition of Pyrazoline-5-ones to Isatine Full article

Journal Journal of The Electrochemical Society
ISSN: 0013-4651 , E-ISSN: 1945-7111
Output data Year: 2014, Volume: 161, Number: 6, Pages: G48-G53 Pages count : DOI: 10.1149/2.104406jes
Authors Elinson M.N. 1 , Merkulova V.M. 1 , Ilovaisky A.I. 1 , Chizhov A.O. 1 , Barba F. 2 , Batanero B. 2
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, 119991 Moscow, Russia
2 Department of Organic Chemistry, University of Alcalá de Henares, Madrid 28871, Spain

Abstract: The electrolysis of pyrazoline-5-ones and isatins in alcohols in an undivided cell results in the fast (16 min.) and efficient formation of the substituted 3-hydroxy-3-(3-hydroxy-5-methyl-1H-pyrazol-4-yl)indol-2-ones in 77-95% substance yields and 1540-1900% current efficiency. This novel electrocatalytic chain process opens a fast efficient and convenient way to functionalized 3-hydroxy-3-(3-hydroxy-5-methyl-1H-pyrazol-4-yl)indol-2-ones – the promising compounds for the different biomedical applications. Thus, the simple electrocatalytic system can produce in aprotic solvent in an undivided cell, under mild conditions the electrochemically induced aldol reaction of isatins and pyrazoline-5-ones.
Cite: Elinson M.N. , Merkulova V.M. , Ilovaisky A.I. , Chizhov A.O. , Barba F. , Batanero B.
Electrocatalytic Fast and Efficient Aldol Addition of Pyrazoline-5-ones to Isatine
Journal of The Electrochemical Society. 2014. V.161. N6. P.G48-G53. DOI: 10.1149/2.104406jes WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000339508600104
Scopus: 2-s2.0-84904812712
OpenAlex: W2001326484
Citing:
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OpenAlex 12
Scopus 11
Web of science 12
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