Tandem Diels–Alder/Coupling Reaction Involving Two Arynes: Highly Stereoselective Synthesis of Dihydronaphtho‐Fused Oxindole
Asian Journal of Organic Chemistry2014Vol. 3(3), pp. 269–272
Citations Over TimeTop 24% of 2014 papers
Abstract
Abstract The reaction of arylidenoxindole and arynes formed in situ was investigated. Two arynes participated in the Diels–Alder cycloaddition and coupling reactions, thus providing quick and efficient access to structurally unusual dihydronaphtho‐fused oxindoles. The present strategy also demonstrates its excellent stereoselectivity and convenient experimental set‐up.
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