67803-94-5

Upstream product

• 61025-08-9 p-methylphenyl 2,3,4-tri-O-acetyl-1-thio-β-D-xylopyranoside 
• 62446-93-9 1,2,3,4-tetra-O-acetyl-D-xylopyranose 
• 87-72-9 D-Xylose 

Downstream Products

• 1173995-02-2 p-tolyl 3,4-di-O-benzoyl-1-thio-β-D-xylopyranoside 
• 1415218-47-1 N-O-[2, 3-di-O-benzoyl-4-O-p-methoxybenzyl-β-D-xylopyranosyl]-L-serine benzyl ester 
• 1415218-48-2 N-acetyl-O-[2,3-di-O-benzoyl-4-O-p-methoxybenzyl-β-D-xylopyranosyl]-L-serine benzyl ester 
• 1415218-49-3 N-acetyl-O-[2,3-di-O-benzoyl-β-D-xylopyranosyl]-L-serine 
• 1415217-99-0 p-tolyl 2, 3-di-O-benzoyl-4-chloroacetyl-1-thio-β-D-xylopyranose 
• 1415218-01-7 p-tolyl 2,3-isopropylidene-4-p-methoxybenzyl-1-thio-β-D-xylopyranose 
• 1415218-02-8 p-tolyl 4-p-methoxybenzyl-1-thio-β-D-xylopyranose 
• 1415218-03-9 p-tolyl 2,3-di-O-benzoyl-4-p-methoxybenzyl-1-thio-β-D-xylopyranose 
• 1415218-09-5 4-methylphenyl 2,3-di-O-benzoyl-1-thio-β-D-xylopyranoside 
• 1415218-04-0 p-tolyl 2,3-isopropylidene-4-benzyl-1-thio-β-D-xylopyranose 
• 1269466-59-2 p-methylphenyl 4-O-benzyl-1-thio-β-D-xylopyranoside 
• 1415218-05-1 p-tolyl 2,3-di-O-benzoyl-4-benzyl-1-thio-β-D-xylopyranose 
• 1415218-06-2 p-tolyl 2,3-isopropylidene-4-levulinoyl-1-thio-β-D-xylopyranose 
• 1415218-07-3 p-tolyl 4-levulinoyl-1-thio-β-D-xylopyranose 

Relevant academic research and scientific papers

Synthesis and Antiproliferative Activities of OSW-1 Analogues Bearing 2”-O-p-Acylaminobenzoyl Residues?

OSW-1 is a well-known natural saponin with potent antitumor activities. We have designed and prepared a small library of 22 OSW-1 analogues with a variety of p-acylamino-benzoyl groups installed at C2” of the xylose residue, wherein a regioselective (1→3)

Tailormade Polysaccharides with Defined Branching Patterns: Enzymatic Polymerization of Arabinoxylan Oligosaccharides

The heterogeneous nature of non-cellulosic polysaccharides, such as arabinoxylan, makes it difficult to correlate molecular structure with macroscopic properties. To study the impact of specific structural features of the polysaccharides on crystallinity

A Kinsenoside and GoodyerosideA analogs of the preparation and use thereof

The invention discloses a preparation method and application of compounds as shown in formula I and II, and in particular relates to preparation of Kinsenoside or GoodyerosideA analogue and medical application of the Kinsenoside or GoodyerosideA analogue

Chemical synthesis of a heparan sulfate glycopeptide: Syndecan-1

Finishing first: The highly complex structure of the title compound (see picture) was assembled. The protective groups utilized, as well as the sequences for formation of the glycosyl linkages and protecting group removal are critical to the success of the synthesis. This first preparation of a heparan sulfate glycopeptide lays the foundation for accessing other members of this class of molecules. Copyright

Facile synthesis of three bidesmosidic oleanolic acid saponins with strong inhibitory activity on pancreatic lipase

The first synthesis of scabiosaponins E (1), F (2), and G (3), three new oleanolic acid saponins with strong inhibitory activity on pancreatic lipase isolated from the Chinese traditional medicinal herb Scabiosa tschiliensis, was efficiently achieved in an one-pot strategy under the combined use of glycosyl trichloroacetimidates and p-toluene 1-thioglycosides (STol) as donors.