A NEW METHOD FOR THE STEREOSELECTIVE SYNTHESIS OF β-XYLOFURANOSIDE

Abstract
β-Xylofuranosides are stereoselectively synthesized in good yields by the successive treatment of the thiocarbonate, derived from 3,5-di-O-benzyl-D-xylofuranose, with methyl fluorosulfonate and hydroxy compounds in the presence of cesium fluoride.

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