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Original Articles

ADDITIONSREAKTIONEN AN As[dbnd]C- UND P[dbnd]C-DOPPELBINDUNGEN DER 1,3-BENZOXARSOLE UND 1,3-BENZOXAPHOSPHOLE

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Pages 347-356 | Received 28 Dec 1983, Accepted 23 Mar 1984, Published online: 19 Dec 2006
 

Abstract

The title compounds show low reactivity towards electrophiles. Under forced conditions, however, the As[dbnd]C derivative 1a is attacked by methyl iodide and CCl4 to give λ5- and (δ3-dihydro)benzoxarsoles, respectively. Nucleophilic additions take place with “soft” bases while “hard” bases fail to react, thus indicating some aromaticity of the heterocycles. Me3SnH is smoothly added by a radical way.

Die Titelverbindungen sind gegenüber Elektrophilen wenig reaktiv. Unter encrgischen Bedingungen setzt sich das As[dbnd]C-Derivat 1a jedoch mit Methyliodid und CCl4 zu δ5- bzw. (δ3-Dihydro)benzoxarsolen um. Nucleophile Additionen gelingen mit “weichen” Basen, während “harte” Basen nicht reagieren. Dies verweist auf gewisse aromatische Stabilisierung der Heterocyclen. Me3SnH wird leicht radikalisch addiert.

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