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- W2022250528 abstract "Abstract Phenylseleninic anhydride reacts rapidly with indolines at 0° to give, when the β-position is substituted, the corresponding indoles. When the β-position is unsubstituted β-phenylseleno- indoles are formed. These are readily reduced by nickel boride to the parent indole. Tetrahyrdroisoquinoline is dehydrogenated with comparable ease. Phenylseleninic acid is also an efficient agent for these dehydrogenations." @default.
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- W2022250528 date "1982-01-01" @default.
- W2022250528 modified "2023-09-29" @default.
- W2022250528 title "La transformation d'indolines en indoles et d'autres reactions apparentees" @default.
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- W2022250528 doi "https://doi.org/10.1016/s0040-4039(00)85756-1" @default.
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