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- W2040802013 abstract "Resume Par chauffage ou en presence d'etherate de trifluorure de bore, les o- et p-hydroxymethyl-phenols alcoylent les composes indoliques en 3,2 ou 1. Il en est de meme des o-aminomethyl-phenols par chauffage et des o- et p-halomethyl-phenols en milieux aqueux neutre ou acide. Certains produits d'alcoylation en 3 existent sous une forme cyclique et peuvent se transposer thermiquement ou par traitement acide en derive 1- our 2-alcoyle. Un mecanisme faisant intervenir un sel de 3H-indolium comme produit primaire de la reaction rend compte de la nature des produits finaux et permet d'interpreter les transpositions observees. Des 3H-trialcoyl-2,3,3 indoles (indolenines) ont d'ailleurs pu etre isoles avec certains p-hydroxymethyl- et p-halomethyl-phenols." @default.
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- W2040802013 date "1970-01-01" @default.
- W2040802013 modified "2023-10-17" @default.
- W2040802013 title "Alcoylation de composés indoliques par les hydroxyméthyl-, aminométhyl- et halométhyl-phénols" @default.
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- W2040802013 doi "https://doi.org/10.1016/s0040-4020(01)92910-2" @default.
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