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Organocatalytic Asymmetric Dearomatization of 3-Nitroindoles and 3-Nitrobenzothiophenes via Thiol-Triggered Diastereo- and Enantioselective Double Michael Addition Reaction
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Citations
58
References
2019
Year
Novel OrganocatalystsEngineeringAlkene MetathesisContiguous StereocentersOrganic ChemistryCatalysisOrganocatalytic Asymmetric DearomatizationChemistryStereoselective SynthesisAsymmetric CatalysisThiol-triggered Diastereo-Chiral TetrahydrothiopheneindolinesEnantioselective SynthesisBiomolecular Engineering
Organocatalytic asymmetric dearomatization of 3-nitroindoles and 3-nitrobenzothiophenes by reaction with ethyl 4-mercapto-2-butenoate has been developed. A range of chiral tetrahydrothiopheneindolines and tetrahydrothiophenebenzothiophenes bearing three contiguous stereocenters are obtained in high yields with good diastereoselectivities and excellent enantioselectivities. This is the first example of thiol-triggered catalytic asymmetric dearomatization of 3-nitroindoles and 3-nitrobenzothiophenes.
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