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Please use this identifier to cite or link to this item: http://10.10.120.238:8080/xmlui/handle/123456789/538
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dc.contributor.authorJafari E.en_US
dc.contributor.authorChauhan P.en_US
dc.contributor.authorKumar M.en_US
dc.contributor.authorChen X.-Y.en_US
dc.contributor.authorLi S.en_US
dc.contributor.authorvon Essen C.en_US
dc.contributor.authorRissanen K.en_US
dc.contributor.authorEnders D.en_US
dc.date.accessioned2023-11-30T08:40:59Z-
dc.date.available2023-11-30T08:40:59Z-
dc.date.issued2018-
dc.identifier.issn1434193X-
dc.identifier.otherEID(2-s2.0-85044782107)-
dc.identifier.urihttps://dx.doi.org/10.1002/ejoc.201800034-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/538-
dc.description.abstractA new protocol for the organocatalytic asymmetric synthesis of highly functionalized tetrahydrocarbazoles has been developed based on a vinylogous Michael/aldol reaction sequence between 3-(trifluoroacetyl)-2-methyl-indoles and enals. This formal [4+2] annulation occurs by cooperative catalysis between an achiral Brønsted base and a chiral secondary amine organocatalyst to afford tetrahydrocarbazole products bearing three vicinal stereocenters, including a trifluoromethylated tetrasubstituted stereocenter, in excellent yields, diastereo- and enantioselectivities. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.sourceEuropean Journal of Organic Chemistryen_US
dc.subjectAnnulationen_US
dc.subjectAsymmetric synthesisen_US
dc.subjectOrganocatalysisen_US
dc.subjectTetrahydrocarbazolesen_US
dc.subjectTrifluoromethylationen_US
dc.titleOrganocatalytic Asymmetric Synthesis of Trifluoromethylated Tetrahydrocarbazoles by a Vinylogous Michael/Aldol Formal [4+2] Annulationen_US
dc.typeJournal Articleen_US
Appears in Collections:Journal Article

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