Advanced Synthesis & Catalysis · 2019 · 28 citations · 46 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryCatalytic MechanismsHeterocyclic ChemistryOrganic SynthesisEnantioselective CatalysisEnantioselective SynthesisIndole ChemistryMedicinal Chemistry ApplicationsMild Reaction Conditions
Abstract We reported a cupreidine catalyzed enantioselective cascade cyclization reaction of 2‐alkynyl‐3,3‐difluoro‐3 H ‐indole and 2‐mercaptoimidazole under simple and mild conditions. The corresponding chiral gem ‐difluorinated C2‐spiro indolines were obtained in moderate to good yields and enantioselectivities, which could be interesting compounds from synthetic and medicinal chemistry points of view. This work represents the first catalytic enantioselective example of utilizing 2‐alkynyl‐3,3‐difluoro‐3 H ‐indoles as the bis‐electrophiles in a cyclization reaction. magnified image
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Asymmetric Organic Catalysis with Modified Cinchona Alkaloids
Shi‐Kai Tian, Yonggang Chen, Jianfeng Hang et al. · Accounts of Chemical Research · 2004 · 618 citations
Cinchona Alkaloids in Asymmetric Organocatalysis
Tommaso Marcelli, Henk Hiemstra · Synthesis · 2010 · 421 citations