Synthesis and Receptor Binding Evaluation of Clavizepine Analogues with No Ring D Substituents

Assembly of the azepine ring of xantheno[9,1-cd]azepines by electrophilic cyclization of sulfonamide acetals provides access to clavizepine analogues in the form of 2,12b-dihydro- or 4-hydroxy-2,3,4,12b-tetrahydro-1H-xantheno[9,1-cd]azepines, in the latter case producing the trans derivative stereos...

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Veröffentlicht in:Journal of organic chemistry 2006-05, Vol.71 (10), p.3963-3966
Hauptverfasser: de la Fuente, M. Carmen, Pullan, Shirley E, Biesmans, Ilse, Domínguez, Domingo
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container_issue 10
container_start_page 3963
container_title Journal of organic chemistry
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creator de la Fuente, M. Carmen
Pullan, Shirley E
Biesmans, Ilse
Domínguez, Domingo
description Assembly of the azepine ring of xantheno[9,1-cd]azepines by electrophilic cyclization of sulfonamide acetals provides access to clavizepine analogues in the form of 2,12b-dihydro- or 4-hydroxy-2,3,4,12b-tetrahydro-1H-xantheno[9,1-cd]azepines, in the latter case producing the trans derivative stereoselectively. Binding assays for clavizepine and analogues at adrenergic, dopaminergic, and serotonergic receptors are reported.
doi_str_mv 10.1021/jo052320c
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subjects Azepines - chemistry
Chemistry
Exact sciences and technology
Fumariaceae - chemistry
Heterocyclic compounds
Heterocyclic compounds with only one n hetero atom and condensed derivatives
Models, Molecular
Molecular Structure
Organic chemistry
Preparations and properties
Protein Binding
Receptors, Serotonin - chemistry
Xanthenes - chemistry
title Synthesis and Receptor Binding Evaluation of Clavizepine Analogues with No Ring D Substituents
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