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Synthesis of thieno[2′,3′(3′,4′ or 3′,2′):5,6]azepino[2,1‐a]isoindolediones from N‐Thienyl‐2(3)‐ylmethylphthalimides

Identifieur interne : 001361 ( France/Analysis ); précédent : 001360; suivant : 001362

Synthesis of thieno[2′,3′(3′,4′ or 3′,2′):5,6]azepino[2,1‐a]isoindolediones from N‐Thienyl‐2(3)‐ylmethylphthalimides

Auteurs : Pascal Pigeon [France] ; Bernard Decroix [France]

Source :

RBID : ISTEX:6E945CAECF0C8D1D4BE4D004CC0B6FBD8AD81B26

Abstract

Reduction of N‐thienybnethylphthalimides 5a‐e followed by the Wittig reaction gave the substituted acetic acids 8a‐e. Their corresponding acyl chlorides where cyclized in the presence of aluminium trichloride to furnish the cyclic ketones 9a‐e. Treatment of these ketones with bromine followed by triethylamine, or with selenium dioxide led to the thienoazepinoisoindolediones 1a‐e.

Url:
DOI: 10.1002/jhet.5570330123


Affiliations:


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ISTEX:6E945CAECF0C8D1D4BE4D004CC0B6FBD8AD81B26

Le document en format XML

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   |texte=   Synthesis of thieno[2′,3′(3′,4′ or 3′,2′):5,6]azepino[2,1‐a]isoindolediones from N‐Thienyl‐2(3)‐ylmethylphthalimides
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