Publication | Closed Access
Enantioselective synthesis of spirooxindole benzoquinolizines via organo-catalyzed cascade reactions
22
Citations
40
References
2016
Year
Spirooxindole BenzoquinolizinesMedicinal ChemistryEnantioselective SynthesisEngineeringDerivative (Chemistry)Spirooxindole Benzoquinolizine DerivativesSpirooxindole BenzoindolizidineNatural SciencesOrganic ChemistryCatalysisStereoselective SynthesisChemistryPharmacologyAsymmetric CatalysisPharmaceutical ChemistrySpirooxindole Benzoquinolizine
A Michael-Mannich-hemiaminalization-dehydration cascade reaction was developed for the construction of spirooxindole benzoquinolizine derivatives. Additionally, spirooxindole benzoindolizidine was prepared conveniently through a ring-contracted rearrangement reaction from spirooxindole benzoquinolizine.
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