2020
DOI: 10.1002/jhet.3953
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A quick and regioselective access of spirooxindole‐oxazoline by reaction of isatin and isocyanoacetate “on water”

Abstract: A greener, rapid and regioselective “on water” synthesis of spirooxindole‐oxazoline by the reaction of isatin and isocyanoacetate at room temperature is described. The developed protocol has the advantage of being atom‐economical, eco‐friendly, and benign reaction conditions. Broader substrate scope, experimentally simple procedures, and easy purification of products with high yield further make this method attractive. The synthesized compounds have been fully characterized with spectral analysis.

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Cited by 3 publications
(1 citation statement)
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“…of 1,4-diazabicyclo[2.2.2]octane (DABCO) as the base catalyst (Scheme 7). Mild reaction conditions, operational simplicity, easy purification procedure, broad substrate scope, high yield (up to 70%), and high atom economy are the major advantages of this green protocol (Rankan et al, 2020). the catalyst, via condensation reaction between indole 22 and isatin 1 compounds.…”
Section: Water As a Solventmentioning
confidence: 99%
“…of 1,4-diazabicyclo[2.2.2]octane (DABCO) as the base catalyst (Scheme 7). Mild reaction conditions, operational simplicity, easy purification procedure, broad substrate scope, high yield (up to 70%), and high atom economy are the major advantages of this green protocol (Rankan et al, 2020). the catalyst, via condensation reaction between indole 22 and isatin 1 compounds.…”
Section: Water As a Solventmentioning
confidence: 99%