51433-17-1

Upstream product

• 876659-94-8 methyl-(O²,O³-dibenzyl-O⁴-methyl-O⁶-trityl-β-D-glucopyranoside) 
• 6988-40-5 methyl 2,3-di-O-benzyl-β-D-glucopyranoside 
• 151807-96-4 methyl 2,3-di-O-benzyl-6-O-deoxy-6-iodo-β-D-glucopyranoside 
• 17791-36-5 methyl 2,3-di-O-benzyl-α-D-glucopyranoside 
• 54522-57-5 methyl-2,3-di-O-benzyl-6-O-(4-toluenesulfonyl)-α-D-glucopyranoside 
• 67776-12-9 methyl 2,3-di-O-benzyl-6-chloro-6-deoxy-α-D-glucopyranoside 
• 193287-39-7 methyl 2,3-di-O-benzyl-4-O-methyl-6-O-p-toluenesulfonyl-α-D-glucopyranoside 
• 193287-42-2 methyl 2,3-di-O-benzyl-6-chloro-6-deoxy-4-O-methyl-α-D-glucopyranoside 
• 709-50-2 methyl beta-D-glucopyranoside 
• 156881-26-4 methyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzyl)-β-D-glucopyranoside 
• 117605-33-1 methyl 4,6-O-(4’-methoxybenzylidene)-α-D-glucopyranoside 
• 1319723-49-3 methyl 4,6-O-p-methoxybenzylidene-2,3-di-O-benzyl-β-D-glucopyranoside 
• 1403227-82-6 methyl 2,3-di-O-benzyl-6-O-p-methoxybenzyl-4-O-methyl-β-D-glucopyranoside 
• 51842-38-7 methyl 2,3-di-O-benzyl-6-O-trityl-β-D-glucopyranoside 

Downstream Products

• 102475-61-6 (2S,3S,4S,5R,6R)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-carboxylic acid 
• 124579-83-5 Methyl (methyl 2,3-di-O-benzyl-4-O-methyl-β-D-glucopyranosid)uronate 
• 321907-90-8 3-(4-Methoxyphenyl)propyl methyl 4-O-methyl-α-D-glucopyranosiduronate 

Relevant academic research and scientific papers

Synthesis of l -Pyranosides by Hydroboration of Hex-5-enopyranosides Revisited

Extensive study of the diastereoselective synthesis of l-pyranosides utilizing hydroboration of substituted exo-glucals (5-enopyranosides) obtained from d-sugars is presented. On the basis of this study we present the empirical rules describing the reacti

Chiroptical properties of an alternatingly functionalized cellotriose bearing two porphyrin groups

Right-handedness derived from bisporphyrins attached to a cellotriose backbone at O-6 and O′′-6 positions is revealed for the first time. This cellotriose is proposed as a model of alternatingly functionalized cellulosics, which have promising properties for applications in optoelectronics and molecular receptors owing to the chirality and rigid backbone effects. This journal is

Synthesis of novel amino acid glycoside conjugates

A new class of non-anomeric amino acid glycoconjugates can be prepared starting from either ω-amino- or ω-halodeoxyglucosides. Treatment of an ether-protected methyl 7-amino-6,7-dideoxy-α-D-glucoheptopyranoside with methyl aspartate isocyanate gave an urea-linked conjugate of methyl glucoheptopyranoside and aspartic acid. Nucleophilic displacement of the ether-protected methyl 6-chloro-6-deoxy-α-D-glucopyranoside with potassium succinimide followed by imide ring opening and amidation of the succinic acid monoamide with dimethyl iminodiacetate led to a conjugate of methyl 6-amino-6-deoxy-α-D-glucopyranoside and iminoodiacetate bridged by succinate.

SYNTHESIS OF A PRECURSOR OF 3-O-(2-ACETAMIDO-2-DEOXY-3-O-METHYL-α-D-GALACTOPYRANOSYL)-4-O-(4-O-METHYL-β-D-GLUCOPYRANOSYLURONIC ACID)-L-FUCOSE

The glycosphingolipids isolated from spermatozoa of a fresh-water bivalve, Hyriopsis schlegelii, have a unique structure containing one or two mannosyl residues, novel linkages including an internal fucopyranosyl residue, as well as terminal xylosyl and 4