Synthesis of benzo(or furo)[5,6]azepino[2,1-a]isoindolone derivatives: π-cyclisations of N -acyliminium ions
Identifieur interne : 000425 ( Istex/Curation ); précédent : 000424; suivant : 000426Synthesis of benzo(or furo)[5,6]azepino[2,1-a]isoindolone derivatives: π-cyclisations of N -acyliminium ions
Auteurs : Adam Daïch [France] ; Stefan Marchalin [Slovaquie] ; Pascal Pigeon [France] ; Bernard Decroix [France]Source :
- Tetrahedron Letters [ 0040-4039 ] ; 1998.
Abstract
Benzo(or furo)[5,6]azepino[2,1-a]isoindolone and derivatives were obtained easily in one-pot via N-acyliminium ions by treatment of 2-(2-methoxycarbonylbenzyl(or fur-3-yl))phthalimide with alkylmagnesium iodide followed by an acidic hydrolysis.
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DOI: 10.1016/S0040-4039(98)02075-9
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<front><div type="abstract" xml:lang="en">Benzo(or furo)[5,6]azepino[2,1-a]isoindolone and derivatives were obtained easily in one-pot via N-acyliminium ions by treatment of 2-(2-methoxycarbonylbenzyl(or fur-3-yl))phthalimide with alkylmagnesium iodide followed by an acidic hydrolysis.</div>
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