Enediynyl ethyl ethers can be thermally decomposed to produce enyne-ketenes. The thermolysis of these ethers usually involves heating the compound to a certain temperature, which initiates a rearrangement reaction. The exact mechanism may vary depending on the specific enediynyl ether structure, but generally, it proceeds through a retro-ene reaction. The thermolysis typically generates an intermediate known as an enyne-ketene, which can be further used in various organic transformations, including cycloadditions, [2+2] cycloadditions, and other reactions to synthesize complex organic molecules.
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