An efficient and mild vinylation of O-, S-, and N-nucleophiles is reported. Copper(I) iodide/ethyl 2-oxocyclohexanecarboxylate is used as the catalytic system. The protocol tolerates a broad range of functional groups on the substrates, and gives the corresponding aryl styryl ethers, aryl styryl sulfides, and N-styrylimidazoles in moderate to excellent yields as well as with good stereoselectivity.
报道了一种高效且温和的O、S和N亲核试剂的
乙烯化反应。使用
碘化
铜(I)/乙基
2-氧代环己烷羧酸酯作为催化体系。该方法对底物上的广泛功能基团具有良好的耐受性,并能够中等至优良产率生成相应的芳基斯蒂尔醚、芳基斯蒂尔
硫化物和N-斯蒂尔
咪唑,且具有良好的立体选择性。