alexa Abstract | Intermolecular (4+3) cycloaddition reactions: Anthracene and its derivatives as dienes

Journal of Chemical and Pharmaceutical Research
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The (4+3)cycloaddition reactions of allylic cations to dienes is a powerful method for the direct synthesis of sevenmembered rings which are occurrence in many of natural products have biological activity. (4+3) cycloadditions reactions between oxyallyl cations and anthracene or 9-substituted anthracene have not yet been studied extensively. Although these compounds have great importance, where 9,10-dihydro-9,10-propano-anthraceness can be used as key step in the medicinal synthesis. For this reason In this review article we will emphasis on the reactions between anthracene and its derivatives as dienes with α,α'-dihaloketones and α,α,α',α'-tetrahaloketones as oxyallyl cations.

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Author(s): Adel AlSaeedi Usama Karama Mujeeb A Sultan and Mazahar Farooqui


oxyallyl cations, dienes, (4+3) cycloaddition, seven-membered rings, anthracene, Anthracene and its derivatives

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