87256-58-4

Upstream product

• 71748-62-4 2-O-Methyl-methyl-β-D-fucopyranosid 
• 100-39-0 benzyl bromide 
• 75-08-1 ethanethiol 
• 71695-47-1 (3aS,4R,6R,7R,7aS)-6,7-Dimethoxy-2,2,4-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 73111-71-4 (3aR,4S,6R,7R,7aR)-4-Bromomethyl-6-methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-ol 
• 110715-29-2 methyl 4,6-O-benzylidene-2-O-methyl-α-D-glucopyranoside 
• 110618-67-2 Methanesulfonic acid (2R,3R,4R,5R,6S)-4-benzyloxy-2-methanesulfonyloxymethyl-5,6-dimethoxy-tetrahydro-pyran-3-yl ester 
• 109280-62-8 methyl 3-O-benzyl-4,6-O-benzylidene-2-O-methyl-α-D-glucopyranoside 
• 82160-01-8 methyl 3-O-benzyl-6-deoxy-2-O-methyl-D-arabino-hexopyranosid-4-ulose 
• 95058-34-7 methyl 3-O-benzyl-6-deoxy-2-O-methyl-α-D-glucopyranoside 
• 110594-89-3 3,4,6-tri-O-acetyl-2-O-methyl-1-deoxy-1-piperidino-β-D-glucose 
• 2140-41-2 2-O-methyl-D-glucopyranose 
• 50705-62-9 methyl 3-O-benzyl-2-O-methyl-α-D-glucopyranoside 
• 81024-47-7 methyl 2-O-methylglucopyraniside 

Downstream Products

• 120264-67-7 (2S,3R)-2-((1S,2R)-1-Benzyloxy-3,3-bis-ethylsulfanyl-2-methoxy-propyl)-3-methyl-1,4-dioxa-spiro[4.5]decane 
• 120329-89-7 Ethyl D-galacto-5-(benzyloxy)-6,7-dihydroxy-4-methoxyoct-2(E)-enoate 6,7-cyclohexyl ketal 
• 87256-56-2 (2R,3S)-3-Benzyloxy-2-methoxy-3-((2S,3R)-3-methyl-1,4-dioxa-spiro[4.5]dec-2-yl)-propionaldehyde 

Relevant academic research and scientific papers

Aureolic acid antibiotics: Synthesis of the cyclohexenone segment from D-glucose

The cyclohexenone segment which is common to all the aureolic acid group of antibiotics has been synthesised from D-glucose.Two routes have been designed to obtain methyl 3-O-benzyl-6-deoxy-2-O-methyl-D-galactopyranoside.Route-A involves the introduction

Aureolic Acid Group of Antibiotics: A Stereospecific Synthesis of Side Chain of Aglycone

A stereospecific synthesis of the side chain (4) present in the aureolic acid group of antibiotics, starting from a D-glucose derivative (5) is described.

Studies on the Synthesis of Olivin: Diastereoselective Synthesis of a Functionalized D-Fucose Derivative

A short, highly diastereoselective synthesis of D-fucose derivative 4 by a route involving the addition of allylboronate reagent 7 to aldehyde 6 is described.