LeHavreV1, Main, Exploration, bibRecord, 001B63

Synthesis of benzo(or furo)[5,6]azepino[2,1-a]isoindolone derivatives: π-cyclisations of N -acyliminium ions

Identifieur interne : 001B63 ( Main/Exploration ); précédent : 001B62; suivant : 001B64

Synthesis 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.

RBID : ISTEX:C7A65F4D756342452E5EC8C8220A6AD38D2A78F5

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.

Url:

https://api.istex.fr/document/C7A65F4D756342452E5EC8C8220A6AD38D2A78F5/fulltext/pdf

DOI: 10.1016/S0040-4039(98)02075-9

Affiliations:

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to stream Istex, to step Curation: 000425
to stream Istex, to step Checkpoint: 000B39
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to stream Main, to step Curation: 001B63

Le document en format XML

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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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Synthesis of benzo(or furo)[5,6]azepino[2,1-a]isoindolone derivatives: π-cyclisations of N -acyliminium ions

Synthesis of benzo(or furo)[5,6]azepino[2,1-a]isoindolone derivatives: π-cyclisations of N -acyliminium ions

Source :

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

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