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Title: AuCl3-AgOTf promoted O-glycosylation using anomeric sulfoxides as glycosyl donors at room temperature. Author: Palanivel A, Chennaiah A, Dubbu S, Mallick A, Vankar YD. Journal: Carbohydr Res; 2017 Jan 02; 437():43-49. PubMed ID: 27912141. Abstract: Activation of sulfoxide as glycosyl donors using AuCl3/AgOTf reagent system has been described. Under optimal reaction conditions, both armed and disarmed glycosyl sulfoxide donors were found to react with a range of primary, secondary, and tertiary alcohol acceptors, and sugar derived glycosyl acceptors to afford the corresponding glycosides in moderate to good yields with predictable selectivity. The reactions are quick (20-60 min), facile at room temperature and the reactions conditions tolerate acid sensitive groups.[Abstract] [Full Text] [Related] [New Search]