82160-01-8

Upstream product

• 82159-78-2 methyl 3-O-benzyl-6-deoxy-2-O-methyl-α-D-altropyranoside 
• 95058-34-7 methyl 3-O-benzyl-6-deoxy-2-O-methyl-α-D-glucopyranoside 
• 110594-92-8 methyl 3-O-benzyl-6-deoxy-2-O-methyl-β-D-glucopyranoside 
• 6752-76-7 methyl 4,6-O-benzylidene-2-O-methyl-α-D-altropyranoside 
• 95058-33-6 methyl 3-O-benzyl-2-O-methyl-6-O-p-tolylsulfonyl-α-D-glucopyranoside 
• 50705-60-7 Methyl 3-O-benzyl-4.6-O-benzyliden-2-O-methyl-α-D-glucopyranosid 
• 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 
• 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 
• 110715-30-5 methyl 4,6-O-benzylidene-2-O-methyl-β-D-glucopyranoside 

Downstream Products

• 82160-03-0 methyl 3-O-benzyl-6-deoxy-4-C-methyl-2-O-methyl-α-D-idopyranoside 
• 101155-55-9 (2S,3S,4R,6R)-4-Benzyloxy-2,3-dimethoxy-6-methyl-5-methylene-tetrahydro-pyran 
• 95058-61-0 (2R,3R,4R,5R,6S)-4-Benzyloxy-5,6-dimethoxy-2,3-dimethyl-tetrahydro-pyran-3-ol 
• 87256-58-4 3-O-benzyl-6-deoxy-2-O-methyl-D-galactose diethyldithioacetal 
• 95058-34-7 methyl 3-O-benzyl-6-deoxy-2-O-methyl-α-D-glucopyranoside 
• 110594-91-7 methyl 3-O-benzyl-6-deoxy-2-O-methyl-α-D-ggalactopyranoside 
• 71695-51-7 methyl 3-O-benzyl-6-deoxy-2-O-methyl-α-D-glucopyranoside 
• 110594-92-8 methyl 3-O-benzyl-6-deoxy-2-O-methyl-β-D-glucopyranoside 
• 101155-57-1 (4R,6S,7S,8R)-8-Benzyloxy-1,1-dichloro-6,7-dimethoxy-4-methyl-5-oxa-spiro[2.5]octane 
• 82160-02-9 methyl 3-O-benzyl-6-deoxy-4-C-methyl-2-O-methyl-α-D-altropyranoside 

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.

SYNTHESIS OF 2,3-ANHYDRO- AND 3,4-ANHYDRO-HEXOPYRANOSIDES HAVING A METHYL BRANCH ON THE OXIRANE RING, AND THEIR REACTIONS WITH SOME LITHIUM METHYLCUPRATE REAGENTS

Three 2,3-anhydroaldohexopyranosides having a 2-C-methyl or 3-C-methyl branch, as well as three 3,4-anhydroaldohexopyranosides having a 3-C-methyl (7) or 4-C-methyl branch, were newly synthesized.The reactions of these, together with those of a known 3-C-

STEREOSELETIVITIES IN THE REACTIONS OF α-D-HEXOPYRANOSID-4-ULOSES WITH DIAZOMETHANE

The stetreoselectivities in the reactions of diazomethane with various α-D-hexopyranosid-4-uloses are compared with those in Grignard reactions.The results support the hypothesis that the stereoselectivity of the diazomethane reaction is mainly controlled