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Enders surveys the literature by systematically considering multiple retrosynthetic disconnects for assembling isoindolones. Using his nomenclature from the aforementioned citation, Method II and Method VIII would involve the formation of a bond between the carbon to nitrogen and the ortho -C-aryl carbon (red bond designated in Scheme, structure 5).
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The stilbene is thought to arise from nucleophilic attack at the benzylic chloride of the acid chloride/imine adduct by another molecule of adduct which has been deprotonated at the a-chlorobenzylic position. Elimination of chloride from the resulting chloro-substituted 1,2-diphenylethane would then afford the stilbene. See
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