23110-90-9

Upstream product

• 22860-25-9 methyl 2,3-dideoxy-4,6-dihydroxy-α-D-erythro-hex-2-enopyranoside 
• 98-88-4 benzoyl chloride 
• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 3169-98-0 methyl 4,6-O-benzylidene-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 

Downstream Products

• 343930-10-9 Benzoic acid (2R,3S,6S)-3-methanesulfonyloxy-6-methoxy-3,6-dihydro-2H-pyran-2-ylmethyl ester 
• 1241380-55-1 methyl 6-O-benzoyl-4-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 343930-11-0 6-Methoxy-3,6-dihydro-2H-pyran-2-carbaldehyde 

Relevant academic research and scientific papers

Effective and chemoselective glycosylations using 2,3-unsaturated sugars

Glycosyl donors containing a double bond between C2 and C3 were designed by mimicking the reaction mechanism of lysozyme-initiated hydrolysis of mucopolysaccharides. It was found that, under various glycosylation conditions, the reactivities of 2,3-unsatu

Total synthesis of S-(+)-argentilactone

Asymmetric total synthesis of S-(+)-argentilactone (2) was accomplished, using methyl-α-D-glucopyranoside (3) as carbohydrate template. Benzylidene acetal 5 was hydrolysed with tBuOOH/AlCl3 and further manipulated to produce the alde