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A new method for α-selective glycosylation using a donor, glycosyl methyldiphenylphosphonium iodide, without any assistance of acid promoters

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CHEMISTRY LETTERS
卷 32, 期 10, 页码 900-901

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CHEMICAL SOC JAPAN
DOI: 10.1246/cl.2003.900

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A mild and highly alpha-selective glycosylation of several glycosyl acceptors was performed with an in situ formed glycosyl donor, benzyl-protected glycosyl methyldiphenylphosphonium iodide, to afford the corresponding alpha-disaccharides in high yields in CH2Cl2 at room temperature without any assistance of acid promoters.

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