New System of Deprotection Step for the Hydroxide Radicals: Boron Trifluoride Etherate/Sodium Iodide
Abstract
A new efficient method for dealkylation of ethers is reported. Ethers could transform into corresponding alcohols with boron trifluoride etherate and sodium iodide in acetonitrile after hydrolysis. This reaction can proceed at room temperature, and the yield is excellent. It’s useful for deprotection process in organic synthesis.
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International Journal of Chemistry ISSN 1916-9698 (Print) 1916-9701 (Online)
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International Journal of Chemistry


