Publication | Closed Access
Copper(I)-Catalyzed Kinetic Resolution of <i>N</i>-Sulfonylaziridines with Indoles: Efficient Construction of Pyrroloindolines
110
Citations
75
References
2015
Year
Asymmetric CatalysisChemical EngineeringNovel OrganocatalystsEngineeringKinetic ResolutionFirst Lewis AcidOrganic ChemistryOrganometallic CatalysisCatalysisChiral PyrroloindolinesChemistryHeterocycle ChemistryStereoselective SynthesisEfficient Construction/Chiral Diphosphine ComplexesSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The first Lewis acid catalyzed [3 + 2] annulation of indoles and 2-aryl-N-tosylaziridines was realized by using copper(I)/chiral diphosphine complexes as a catalyst. With this method, a variety of uniquely substituted chiral pyrroloindolines bearing multiple contiguous stereogenic centers were facilely accessed in a straightforward, high-yielding, and highly stereoselective way under mild conditions.
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