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- W2118618381 abstract "Abstract A concise and efficient total synthesis of Secobatzelline B is reported. The synthesis involves eight steps starting from known 4,6,7‐trimethoxyindole. Synthetic tactics involve a one‐step reduction of an indole‐3‐glyoxalic ester using LiAlH4, resulting in complete reduction of the ester group and a partial reduction of the vinylogous amide carbonyl group. Synthesis also involves the use of a mixture of NaCl and oxone as a new reagent for regioselective chlorination of an indoloquinone derivative." @default.
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- W2118618381 date "2007-07-01" @default.
- W2118618381 modified "2023-09-26" @default.
- W2118618381 title "Total Synthesis of Secobatzelline B" @default.
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- W2118618381 doi "https://doi.org/10.1080/00397910701410954" @default.
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