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- W2151587868 abstract "1-Cyano-2,2-diethoxycarbonyl cyclopropane was reacted with several nitroarenes under basic conditions. The reaction proceeded according to the vicarious nucleophilic substitution of hydrogen scheme; i.e. the initially formed σ-adducts underwent base-induced elimination, resulting in cleavage of the cyclopropane ring. The ortho-substituted products can be directly transformed into substituted N-hydroxyindoles." @default.
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- W2151587868 date "1998-12-01" @default.
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- W2151587868 title "The vicarious nucleophilic substitution of hydrogen proceeding via a cyclopropane ring-opening" @default.
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- W2151587868 doi "https://doi.org/10.1016/s0040-4039(98)02114-5" @default.
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