95898-07-0

Upstream product

• 1856-05-9 cholesterol trimethylsilyl ether 
• 95898-05-8 2,3,4-tri-O-benzyl-α-D-xylopyranosyl fluoride 
• 57-88-5 cholesterol 
• 95898-04-7 1-O-acetyl 2,3,4-tri-O-benzyl-α,β-D-xylopyranose 
• 18039-26-4 2,3,4-tri-O-benzyl-D-xylopyranose 
• 121916-92-5 2,3,4-tri-O-benzyl-α-D-xylopyranosyl chloride 

Relevant academic research and scientific papers

THERMAL GLYCOSIDATION WITH BENZYLATED GLYCOSYL CHLORIDES: A VERY SIMPLE PROCEDURE FOR O-GLYCOSIDATION

Thermal condensation of benzylated glucosyl chlorides with a variety of alcohols has been achieved efficiently without using any metal salts via a simple operation, and the procedure is used not only for a glucosyl halide, but also for a xylosyl chloride. KEYWORDS O-glycosidation; thermal glycosidation; glucosyl chloride; xylosyl chloride; disaccharide

Stereoselective Glycosylation of Alcohols and Silyl Ethers Using Glycosyl Fluorides and Boron Trifluoride Etherate

The stereoselective glycosylation of alcohols and their silyl ethers has been achieved using O-alkyl-, O-acyl-, and acetal-protected glycosyl fluorides of the pyranose and furanose series and boron trifluoride etherate in CH2Cl2.