129575-88-8

Usage

Chemical Properties

White to light yellow solid

InChI:InChI=1/C35H31NO8/c1-39-24-16-18-25(19-17-24)42-35-29(36-32(37)26-14-8-9-15-27(26)33(36)38)31(40-20-22-10-4-2-5-11-22)30-28(43-35)21-41-34(44-30)23-12-6-3-7-13-23/h2-19,28-31,34-35H,20-21H2,1H3/t28-,29-,30-,31-,34-,35-/m1/s1

Upstream product

• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose 
• 85-44-9 phthalic anhydride 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranose 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 150-76-5 4-methoxy-phenol 
• 138906-42-0 p-Methoxyphenyl 2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-41-9 4-methoxylphenzyl 2-deoxy-2-phthalimido-3,4,6-tri-O-acetyl-β-D-glucopyranoside 
• 138906-43-1 4-methoxyphenyl 4,6-di-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 140615-77-6 4-methoxyphenyl 4-O-acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 129575-90-2 p-Methoxyphenyl O-(2,4-di-O-acetyl-3,6-di-O-allyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 129575-91-3 p-Methoxyphenyl O-(6-O-acetyl-2,4-di-O-benzyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 129575-84-4 O-(6-O-Acetyl-2,4-di-O-benzyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate 
• 138906-46-4 p-Methoxyphenyl O-(2,4-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-53-3 p-Methoxyphenyl O-(2,4-di-O-benzyl-6-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138935-14-5 p-Methoxyphenyl O-(2,4-di-O-benzyl-3-O-levulinoyl-6-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 134296-64-3 O-(2,4-di-O-Benzyl-3-O-levulinoyl-6-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate 
• 138935-12-3 p-Methoxyphenyl O-(3,6-di-O-allyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-47-5 p-Methoxyphenyl O-(6-O-acetyl-2,4-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-45-3 p-Methoxyphenyl O-(3,6-di-O-allyl-2,4-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 866635-77-0 4-methoxyphenyl O-(3,6-di-O-acetyl-2,4-di-O-benzyl-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 

Relevant academic research and scientific papers

Chemoenzymatic approach for the preparation of asymmetric bi-, tri-, and tetra-antennary N-glycans from a common precursor

Progress in glycoscience is hampered by a lack of well-defined complex oligosaccharide standards that are needed to fabricate the next generation of microarrays, to develop analytical protocols to determine exact structures of isolated glycans, and to elu

NOVEL INTERMEDIATES FOR THE PREPARATION OF GBS POLYSACCHARIDE ANTIGENS

The present invention generally refers to novel intermediate polysaccharide units, useful for the preparation of polysaccharide antigen of GBS Ia, Ib and III; the invention also refers to a process for their preparation and their use as intermediate for t

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A new and efficient Ionic Liquid-Supported Oligosaccharide Synthesis (ILSOS) strategy for an N-linked core pentasaccharide on a 10 g scale is reported. This new ILSOS includes a new spacer for an IL support, a new tagging strategy, and fast, efficient and orthogonal removal of the ionic-liquid support, producing the N-linked core pentasaccharide with direct applicability potential in a short time, with high yield and on a large gram scale.

REAGENTS AND METHODS FOR GLYCOSYLATION

The invention provides methods and regents for the glycosylation of organic molecules. In one aspect, the invention provides a method for glycosylating a hydroxyl-containing organic compound (i.e., a glycosyl acceptor) comprising contacting a glycosyl don

Preparation of Thiosugars and Their Use

A process for the preparation of a thiosaccharide represented by Saccharide-S-H wherein Saccharide comprises at least 4 sugar units, comprises subjecting a corresponding compound of the formula (P)Saccharide-S-(P) wherein (P) represents an O- or S-protecting group(s), to Birch reduction.

Synthesis of sulfated glucuronyl glycosphingolipids; carbohydrate epitopes of neural cell-adhesion molecules

The sulfated glucuronyl glycosphingolipids isolated from the human peripheral nervous system, HO3S-3-β-GlcpA-(1 → 3)-{β-D-Galp-(1 → 4)-β-D-GlcpNAc-(1 → 3)}(n)-β-D-Galp-(1 → 4)-β-D-Glcp-(1 → 1)-Cer (n = 1, 2) (1 and 2) were synthesized. The glyc

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A total synthesis of a sulfated glucuronyl glycosphingolipid isolated from human peripheral nervous system was achieved for the first time.