Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 24, Pages 2878-2879Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b412823k
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The reactions of methylenecyclopropanes 1 with diphenyl diselenide give ring-opened products 2 in good yields at 150 degreesC under nitrogen atmosphere for 3 h; the products 2 can further undergo oxidative cyclization with hydrogen peroxide to furnish 3-phenylselenyl-2,5-dihydrofurans 3 in moderate yields ( three steps) at room temperature in CH2Cl2 for 5 h; a plausible reaction mechanism has been proposed.
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