Silylation de dérivés gem-dihalogénés bicycliques: synthèse de dihydro- et tétrahydro-oxépines siliciées

The silylation of 2-oxa-7,7′-dichloronorcarane has been studied. According to the reagent (Me 3 SiCl/Li/THF or MeSi 3 Cl/Mg/HMPT), we observed significant differences in the reactivity, and silyloxabicyclonorcaranes or silylhydrooxepines were obtained. The influence of solvant and experimental condi...

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Veröffentlicht in:Canadian journal of chemistry 1991-12, Vol.69 (12), p.2014-2017
Hauptverfasser: Grignon-Dubois, Micheline, Fialeix, Michelle, Biran, Claude
Format: Artikel
Sprache:eng
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Zusammenfassung:The silylation of 2-oxa-7,7′-dichloronorcarane has been studied. According to the reagent (Me 3 SiCl/Li/THF or MeSi 3 Cl/Mg/HMPT), we observed significant differences in the reactivity, and silyloxabicyclonorcaranes or silylhydrooxepines were obtained. The influence of solvant and experimental conditions is discussed. Key words: silylation, hydrooxepine skeleton.
ISSN:0008-4042
1480-3291
DOI:10.1139/v91-291