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- W2322358718 endingPage "140" @default.
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- W2322358718 abstract "A microwave-assisted regioselective reaction dealing with arylglyoxal monohydrate, diverse N-aryl enaminones, and indoles to achieve 3,2'- and 3,3'-bis-indoles by varying a substituted indole substrate is reported. The 2-unsubstituted indoles resulted in the 3,2'-bis-indole skeleton, whereas indoles bearing a methyl or phenyl group at C2 led to the 3,3'-bis-indoles with simultaneous formation of three sigma-bonds. The procedures feature excellent regioselectivity, short reaction times, convenient one-pot manner, and operational simplicity." @default.
- W2322358718 created "2016-06-24" @default.
- W2322358718 creator A5004392744 @default.
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- W2322358718 date "2013-01-31" @default.
- W2322358718 modified "2023-10-17" @default.
- W2322358718 title "Three-Component Domino Reactions for Regioselective Formation of Bis-indole Derivatives" @default.
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- W2322358718 doi "https://doi.org/10.1021/co3001428" @default.
- W2322358718 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23339825" @default.
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