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- W2026474420 abstract "A new method for conversion of 3-alkylindoles to 3-alkyl-2-amino-3H-indol-3-ols is described. In this reaction, the indole nucleus was first oxidized with ozone to alkyl 2-formamidophenyl ketone, which was subsequently subjected to the reaction with cyanide ion in weakly alkaline medium to cyclize to the 3H-indole ring. The overall yield of the reaction was approximately 75 %. By this method an ionizable amidine function was introduced at the side chain of tryptophan." @default.
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- W2026474420 date "1979-05-05" @default.
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- W2026474420 title "CONVERSION OF 3-ALKYLINDOLE TO 3-ALKYL-2-AMINO-3<i>H</i>-INDOL-3-OL VIA ALKYL 2-FORMAMIDOPHENYL KETONE" @default.
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- W2026474420 doi "https://doi.org/10.1246/cl.1979.587" @default.
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