56933-07-4

Upstream product

• 140420-69-5 allyl α-D-xylopyranoside 
• 96789-04-7 1,2,3,4-tetra-O-benzoyl-D-xylopyranose 
• 145374-03-4 tri-O-benzoyl-ξ-D-xylopyranosyl bromide 
• 14262-83-0 2,3,4-tri-O-benzoyl-α-D-xylopyranosyl bromide 
• 30319-44-9 1,2,3,4-tetra-O-benzoyl-α-D-xylopyranose 
• 6763-34-4 D-xylose 
• 87-72-9 D-Xylose 
• 98-88-4 benzoyl chloride 
• 1423987-82-9 2,3,4-tri-O-benzoyl-N-methoxy-N-methyl-β-D-xylopyranosylamine 
• 502765-01-7 allyl 3-O-benzoyl-α-D-xylopyranoside 
• 502765-02-8 allyl 2,3,4-tri-O-benzoyl-α-D-xylopyranoside 

Downstream Products

• 351900-98-6 O-4-methoxybenzyl-O-[(2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->2)]-O-[(2,3,4-tri-O-benzoyl-β-D-xylosyl)-(1->3)]-6-O-methyl-4-O-acetyl-β-D-glucuronate 
• 432519-23-8 2,3,4-tri-O-benzoyl-α-D-xylopyranosyl trichloroacetimidate 
• 502765-04-0 2,3,4-tri-O-benzoyl-α,β-D-xylopyranosyl trichloroacetimidate 
• 1423987-82-9 2,3,4-tri-O-benzoyl-N-methoxy-N-methyl-β-D-xylopyranosylamine 
• 145374-03-4 tri-O-benzoyl-ξ-D-xylopyranosyl bromide 
• 3862-87-1 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl fluoride 
• 4163-50-2 Tri-O-benzoyl-α-D-xylopyranosylfluorid 

Relevant academic research and scientific papers

Synthesis of the hyper-branched core tetrasaccharide motif of chloroviruses

Chemical synthesis of complex oligosaccharides, especially those possessing hyper-branched structures with one or multiple 1,2-cisglycosidic bonds, is a challenging task. Complementary reactivity of glycosyl donors and acceptors and proper tuning of the s

Delta-oleanolic acid saponin compound and medical application thereof

The invention discloses a delta-oleanolic acid saponin compound and medical application thereof. The delta-oleanolic acid saponin compound is a compound with a structural formula shown as a formula (I), and pharmaceutically acceptable salt or ester or pro

Total syntheses of schizandriside, saracoside and (±)-isolariciresinol with antioxidant activities

Lignans are widely distributed in plants and exhibit significant pharmacological effects, including anti-tumor and antioxidative activities. Here, we describe the total synthesis of schizandriside (1), a compound we previously isolated from Saraca asoca b

Convergent strategy for the synthesis of S-linked oligoxylans

Arabinoxylans (AX) are a major class of hemicellulose and an important polysaccharide component of lignocellulosic biomass. To utilize the glycan polymer effectively, it is desirable to learn more about the enzymatic hydrolysis of AXs. Well-defined glycan

THIOPYRANOSE COMPOUND AND METHOD FOR PRODUCING SAME

There is provided a production method of a thiopyranose compound represented by the following Formula (2) by reacting a compound represented by the following Formula (1) with a sulfur compound. X represents a leaving group. A represents an oxygen atom or

Tandem Allylboration-Prins Reaction for the Rapid Construction of Substituted Tetrahydropyrans: Application to the Total Synthesis of (-)-Clavosolide A

Tetrahydropyrans are common motifs in natural products and have now been constructed with high stereocontrol through a three-component allylboration-Prins reaction sequence. This methodology has been applied to a concise (13 steps) and efficient (14 % ove

Facile synthesis of the pentasaccharide repeating unit of the exopolysaccharide from Cryptococcus neoformans serotype D

Abstract β-D-GlcpA-(1→2)-[β-D-Xylp-(1→2)-α-D-Manp-(1→3)]-α-D-Manp-(1→3)-α-D-Manp, the repeating unit of the exopolysaccharide from Cryptococcus neoformans serotype D, was synthesized as its 4-methoxyphenyl glycoside. The approach presented here also provi

Total Synthesis of Linckosides A and B, the Representative Starfish Polyhydroxysteroid Glycosides with Neuritogenic Activities

Linckosides A and B, two starfish metabolites with promising neuritogenic activities, are synthesized in a longest linear sequence of 32 steps and 0.5% overall yield; this represents the first synthesis of members of the polyhydroxysteroid glycoside family, which occur widely in starfishes.

A new method for selective deprotection of anomeric N,O -dimethylhydroxylamine promoted by TMSCl

TMSCl was shown to be an efficient reagent for selective deprotection of the anomeric position protected as N,O-dimethylhydroxylamine glycoside. This deprotection condition was proved to be compatible with a number of protecting groups, such as the TBDPS, acetyl, benzyl, benzylidene, and benzoyl groups.Copyright Taylor and Francis Group, LLC.

Synthesis and evaluation of four hederagenin glycosides as α-glucosidase inhibitor

The four hederagenin glycosides 1-4 were efficiently synthesized through one-pot sequential glycosylations with glycose 1-(trichloroacetimidate)s as donors, resulting in a significantly simplified synthetic procedure without isolation of glycosylation intermediates. The activity of the synthetic hederagenin glycosides 1-4 against α-glucosidase type IV was evaluated; hederagenin glycoside 4 containing an α-L-rhamnopyranosyl unit showed the best activity with an IC50 value of 47.9 μM. Copyright