The Journal of Organic Chemistry · 2015 · 54 citations · 54 references
Natural SciencesChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic Synthesis[4+2] CycloadditionAsymmetric Heterocycle SynthesisChiral Product SynthesisEnantioselective CatalysisEnantioselective SynthesisIndole ChemistryIndole SynthesisLewis Acidity
A highly enantioselective [4+2] annulation with respect to allenoates and 3-olefinic oxindoles catalyzed by Lewis base was reported, which proved to be an efficient way to synthesize chiral dihydropyran-fused indoles. The cycloaddition products were generally obtained in high yields (up to 98%) with very good enantioselectivities (up to 94% enantiomeric excess).
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Nucleophilic Phosphine Organocatalysis
Joey L. Methot, William Roush · Advanced Synthesis & Catalysis · 2004 · 969 citations · Full text