58341-57-4

Upstream product

• 203717-51-5 methyl 2-O-benzyl-3-O-allyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 15038-71-8 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 76375-66-1 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 

Downstream Products

• 142967-65-5 Methyl 3-O-allyl-2-O-benzyl-6-O-p-tolylsulfonyl-α-D-glucopyranoside 
• 58341-58-5 (2R,3R,4S,5R,6S)-4-Allyloxy-3,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran 
• 134311-55-0 Methyl 3-O-allyl-2,4-di-O-benzyl-6-deoxy-α-D-glucopyranoside 
• 142967-66-6 Methyl 3-O-allyl-2,4-di-O-benzyl-6-O-p-tolylsulfonyl-α-D-glucopyranoside 
• 114283-90-8 1,3-Di-O-acetyl-2,4-di-O-benzyl-6-deoxy-α,β-D-glucopyranose 
• 127874-91-3 3-O-allyl-2,4-di-O-benzyl-6-deoxy-α/β-D-glucopyranose 
• 42822-31-1 2,4-Di-O-benzyl-6-deoxy-α,β-D-glucopyranose 
• 141942-25-8 1,3-Anhydro-2,4-di-O-benzyl-β-D-glucopyranose 
• 134311-58-3 3-O-Acetyl-2,4-di-O-benzyl-6-deoxy-α-D-glucopyranosyl chloride 
• 502621-12-7 methyl 3-O-(2-hydroxyethyl)-4-azido-2-O-benzyl-4,6-dideoxy-α-D-glucopyranoside 
• 502621-11-6 methyl 3-O-allyl-4-azido-2-O-benzyl-4,6-dideoxy-α-D-glucopyranoside 
• 502621-10-5 methyl 3-O-allyl-2-O-benzyl-6-deoxy-α-D-galactopyranoside 
• 502621-09-2 methyl 3-O-allyl-2-O-benzyl-6-deoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Exploring the optimal site for modifications of pyranmycins with the extended arm approach.

[reaction: see text] Continuing from the syntheses and the antibacterial studies of a library of pyranmycins, we further probed the proximity around ring III of pyranmycin by introducing an "extended arm" that has hydroxyethyl or aminoethyl groups at the

Synthesis and conformational analysis of substituted 2,6-dioxabicycloheptanes: 1,3-anhydro-2,4-di-O-benzyl-6-deoxy-β-D-glucopyranose by 1H-NMR spectroscopy and molecular mechanics calculation

A highly selective ring opening reduction of methyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside provided the 2,4-di-O-benzyl derivative.This was toluenesulfonylated or iodinated and subsequently reduced to give crystalline methyl 3-O-allyl-