95898-04-7

Upstream product

• 108-24-7 acetic anhydride 
• 18039-26-4 2,3,4-tri-O-benzyl-D-xylopyranose 
• 91-09-8 methyl xyloside 
• 100-39-0 benzyl bromide 
• 242143-00-6 methyl 2,3,4-tri-O-benzyl-D-xylopyranoside 
• 58-86-6 D-xylose 

Downstream Products

• 99701-77-6 2-(2,3,4-Tri-O-benzyl-β-D-xylopyranosyl)-1-propen 
• 99701-77-6 2-(2,3,4-Tri-O-benzyl-α-D-xylopyranosyl)-1-propen 
• 1427178-82-2 N-benzyloxycarbonyl 2,3,4-tri-O-benzyl-α-D-xylopyranosylamine 
• 1427178-83-3 N-benzyloxycarbonyl 2,3,4-tri-O-benzyl-β-D-xylopyranosylamine 
• 95898-07-0 3β-cholesteryl 2,3,4-tri-O-benzyl-α-D-xylopyranoside 
• 95898-07-0 3β-cholesteryl 2,3,4-tri-O-benzyl-β-D-xylopyranoside 
• 88287-92-7 O³-(2,3,4-tri-O-benzyl-α-D-xylopyranosyl)-N²-(benzyloxycarbonyl)-L-serine allyl ester 
• 88287-93-8 O³-(2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-N²-(benzyloxycarbonyl)-L-serine allyl ester 
• 95898-05-8 2,3,4-tri-O-benzyl-α-D-xylopyranosyl fluoride 

Relevant academic research and scientific papers

An improved methodology for the synthesis of 1-C-allyl imino-d-xylitol and -l-arabinitol and their rapid functionalization

As part of our research program dedicated to the design and synthesis of new iminosugars as pharmacological chaperones for the treatment of lysosomal storage disorders, we developed a rapid and efficient methodology for the access to functionalized and no

Stereoselective C-glycosylation reactions of pyranoses: The conformational preference and reactions of the mannosyl cation

A systematic study of C-glycosylations of acetals related to mannose and other pyranoses was conducted. The C-5 alkoxyalkyl group provides only a modest influence on stereoselectivity. On the other hand, studies of pentopyranoses bearing alkoxy groups at

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.