2013
DOI: 10.1039/c2gc36552a
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Three-component stereoselective synthesis of spirooxindole derivatives

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Cited by 100 publications
(36 citation statements)
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References 44 publications
(8 reference statements)
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“…It has been reported that sharing the third-carbon atom of indole in the formation of spirooxindole derivatives highly enhances the biological activity [16][17][18][19]. Compounds with spiro skeleton have shown both constitute subunits in numerous alkaloids and are templates for drug discovery which have been used as scaffolds for combinatorial libraries [20][21][22].…”
Section: Introductionmentioning
confidence: 99%
“…It has been reported that sharing the third-carbon atom of indole in the formation of spirooxindole derivatives highly enhances the biological activity [16][17][18][19]. Compounds with spiro skeleton have shown both constitute subunits in numerous alkaloids and are templates for drug discovery which have been used as scaffolds for combinatorial libraries [20][21][22].…”
Section: Introductionmentioning
confidence: 99%
“…Thus, multicomponent reactions play a significant role in the organic and medicinal synthesis [13][14][15][16][17][18]. The possibility of performing multicomponent reactions under mild conditions with a heterogeneous catalyst could enhance their effectiveness from economic and ecological points of view.…”
Section: Introductionmentioning
confidence: 99%
“…Undoubtedly, the synthesis of naphthopyranopyrimidines through multicomponent reactions (MCRs) has been paid much attention due to excellent synthetic efficiency, inherent atom economy, procedural simplicity and environmental friendliness. [7][8][9][10][11] The eco-friendly, solvent-free multicomponent approach opens up numerous possibilities for environmentally clean synthesis which involves reduction or elimination of the use or generation of hazardous chemicals. [12][13] The possibility of performing multicomponent reactions under solvent-free conditions with a heterogeneous catalyst could improve their cost-effectiveness and ecological acceptability.…”
Section: Antitubercular Activity (Against Mycobacterium Tuberculosis mentioning
confidence: 99%