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- W2035993403 endingPage "7541" @default.
- W2035993403 startingPage "7538" @default.
- W2035993403 abstract "The first highly enantioselective iso-Pictet-Spengler reaction of C-2-linked o-aminobenzylindoles with trifluoromethyl ketones was developed using chiral spirocyclic phosphoric acids as organocatalysts, which afforded optically active benzazepinoindoles bearing trifluoromethylated quaternary stereocenters." @default.
- W2035993403 created "2016-06-24" @default.
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- W2035993403 creator A5084952507 @default.
- W2035993403 date "2014-01-01" @default.
- W2035993403 modified "2023-10-01" @default.
- W2035993403 title "Enantioselective synthesis of benzazepinoindoles bearing trifluoromethylated quaternary stereocenters catalyzed by chiral spirocyclic phosphoric acids" @default.
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- W2035993403 doi "https://doi.org/10.1039/c4cc02295e" @default.
- W2035993403 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24890313" @default.
- W2035993403 hasPublicationYear "2014" @default.
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