Article ID Journal Published Year Pages File Type
5274904 Tetrahedron Letters 2012 4 Pages PDF
Abstract

A facile and convenient synthesis of disarmed glycosyl fluorides using in situ-generated iodine monofluoride is reported. The method is tolerant to most of the popularly used protecting groups and gives exclusively the α-anomeric product in very good yields.

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Physical Sciences and Engineering Chemistry Organic Chemistry
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A facile and convenient synthesis of disarmed glycosyl fluorides using in situ-generated iodine monofluoride (see Ref. 1)
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