502765-01-7

Upstream product

• 98-88-4 benzoyl chloride 
• 140420-69-5 allyl α-D-xylopyranoside 

Downstream Products

• 502765-03-9 allyl 2,4-di-O-benzoyl-α-D-xylopyranoside 
• 502765-02-8 allyl 2,3,4-tri-O-benzoyl-α-D-xylopyranoside 
• 502765-07-3 allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->3)-2,4-di-O-benzoyl-α-D-xylopyranoside 
• 502765-08-4 allyl 2,4-di-O-benzoyl-3-O-chloroacetyl-β-D-xylopyranosyl-(1->3)-2,4-di-O-benzoyl-α-D-xylopyranoside 
• 502765-10-8 allyl 2,4-di-O-benzoyl-β-D-xylopyranosyl-(1->3)-2,4-di-O-benzoyl-α-D-xylopyranoside 
• 432519-23-8 2,3,4-tri-O-benzoyl-α-D-xylopyranosyl trichloroacetimidate 
• 947259-02-1 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl tricholoroacetimidate 
• 502765-05-1 allyl 2,4-di-O-benzoyl-3-O-chloroacetyl-α-D-xylopyranoside 
• 56933-07-4 2,3,4-tri-O-benzoyl-D-xylopyranose 

Relevant academic research and scientific papers

An efficient and practical synthesis of β-(1→3)-linked xylooligosaccharides

A facile and practical method was developed for the synthesis of β-(1→3)-linked xylooligosaccharides. Dibezoylation of allyl α-D-xylopyranoside (1) afforded 2,4-dibenzoate 6 as the major product. Chloroacetylation of 6, followed by deallylation and trichloroacetimidation, gave a 1:3 α/β imidate (10 and 11) mixture. Coupling of the imidate mixture with 6 gave a disaccharide 13, whose dechloroacetylation afforded the disaccharide acceptor 16. Condensation of perbenzoylated xylosyl α/β imidate (7 and 8) mixture with 6 gave the disaccharide 12. Deallylation of 12, followed by trichloroacetimidation, furnished the disaccharide donor as a 1:1 α/β mixture. Coupling of the disaccharide donor mixture with the disaccharide acceptor 16 yielded the tetrasaccharide 17. Reiteration of deallylation and trichloroacetimidation transformed 17 to the tetrasaccharide donor mixture. Condensation of the tetrasaccharide donor mixture with the acceptor 16 gave the hexasaccharide 21. Debenzoylation with saturated ammonia-methanol afforded β-(1→3)-linked allyl xylotetraoside and xylohexaoside.