Publication | Closed Access
An efficient green chemistry protocol for the synthesis of novel spiropyrrolizidine compounds
49
Citations
28
References
2013
Year
EngineeringHeterocyclicEfficient MethodAmbient ConditionsMedicineDrug DiscoveryGreen Chemistry1,3-Dipolar CycloadditionNovel Spiropyrrolizidine CompoundsOrganic ChemistryChemistryHeterocycle ChemistrySynthesis MethodPharmacologySynthetic ChemistryBiomolecular Engineering
An efficient method for the synthesis of spirooxindolopyrrolizidine/spirooxindolothiapyrrolizidine by the 1,3-dipolar cycloaddition of azomethine ylides generated via, decarboxylative condensation of 1,2-dicarbonyl compounds and L-proline/L-thiaproline/sarcosine with chalcones at ambient conditions with excellent yields has been described.
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