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Mendeleev Communications, 2022, Volume 32, Issue 4, Pages 543–545
DOI: https://doi.org/10.1016/j.mencom.2022.07.036
(Mi mendc720)
 

This article is cited in 2 scientific papers (total in 2 papers)

Communications

Noncatalytic on water aldol reaction of isatins with cyclic 1,3-diketones at room temperature without the need for subsequent chromatography

M. N. Elinson, Yu. E. Ryzhkova, V. M. Kalashnikova, M. P. Egorov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Noncatalytic on water aldol transformation of isatins and cyclic 1,3-diketones results in substituted 3-hydroxy-3-(2-hydroxy-6-oxocyclohex-1-en-1-yl)indolin-2-ones in 87–98% yields. Optimized conditions have been found and a mechanistic rationale for the reaction has been deduced. The new efficient and facile process represents a convenient way to compounds with the 3-hydroxyindolin-2-one and 3-hydroxycyclohex-2-en-1-one moieties.
Keywords: aldol reaction, noncatalytic, on water, isatin, 13-diketone, 3-hydroxyindolin-2-one.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.3 Mb)


Citation: M. N. Elinson, Yu. E. Ryzhkova, V. M. Kalashnikova, M. P. Egorov, “Noncatalytic on water aldol reaction of isatins with cyclic 1,3-diketones at room temperature without the need for subsequent chromatography”, Mendeleev Commun., 32:4 (2022), 543–545
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  • This publication is cited in the following 2 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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