Publication | Closed Access
Regioselective Synthesis of Novel Spirooxindolo and Spiroindano Nitro Pyrrolidines Through 3+2 Cycloaddition Reaction
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Citations
16
References
2006
Year
β‐Nitro Styrene ReactsNovel SpirooxindoloEngineeringHeterocyclicAzomethine YlidesNatural SciencesDiversity-oriented SynthesisOrganic ChemistryCycloaddition ReactionRegioselective SynthesisChemistryHeterocycle ChemistryPharmacologySynthetic ChemistryBiomolecular Engineering
β‐Nitro styrene reacts with nonstabilized azomethine ylides generated from isatin/ninhydrin with sarcosine, resulting in the formation of a series of spiroxindolo nitro pyrrolidines, and spiroindano nitro pyrrolidines, respectively, in good yields. It was noted that in a one‐pot 3+2 cycloaddition reaction, the azomethine ylides generated from isatin and ninhydrin have reacted with the β‐nitro styrenes regiochemically in opposite ways.
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