130780-25-5

Upstream product

• 64429-65-8 methyl 3,4-di-O-benzoyl-2,6-dideoxy-β-L-lyxo-hexopyranoside 
• 108-24-7 acetic anhydride 
• 106988-66-3 C₂₀H₂₀O₆ 

Downstream Products

• 136459-98-8 Benzoic acid (R)-2-benzyloxy-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5,9,10-tetramethoxy-anthracen-2-yl}-2-methyl-pent-4-enyl ester 
• 136459-98-8 Benzoic acid (S)-2-benzyloxy-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5,9,10-tetramethoxy-anthracen-2-yl}-2-methyl-pent-4-enyl ester 
• 136459-99-9 Benzoic acid (R)-2-benzyloxy-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5-dimethoxy-9,10-dioxo-9,10-dihydro-anthracen-2-yl}-2-methyl-pent-4-enyl ester 
• 136459-99-9 Benzoic acid (S)-2-benzyloxy-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5-dimethoxy-9,10-dioxo-9,10-dihydro-anthracen-2-yl}-2-methyl-pent-4-enyl ester 
• 136459-97-7 (R)-2-Benzyloxy-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5,9,10-tetramethoxy-anthracen-2-yl}-2-methyl-pent-4-en-1-ol 
• 136459-97-7 (S)-2-Benzyloxy-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5,9,10-tetramethoxy-anthracen-2-yl}-2-methyl-pent-4-en-1-ol 
• 136460-00-9 Benzoic acid (S)-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5-dimethoxy-9,10-dioxo-9,10-dihydro-anthracen-2-yl}-2-hydroxy-2-methyl-pent-4-enyl ester 
• 136460-00-9 Benzoic acid (R)-1-{6-[(2R,4R,5R,6R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yl]-1,5-dimethoxy-9,10-dioxo-9,10-dihydro-anthracen-2-yl}-2-hydroxy-2-methyl-pent-4-enyl ester 
• 136459-92-2 C₃₈H₃₆O₉ 
• 128461-96-1 C₃₀H₂₆O₆ 
• 128461-95-0 C₃₀H₂₆O₆ 
• 128462-02-2 C₃₇H₃₄O₉ 
• 128461-97-2 C₃₀H₂₆O₆ 
• 128461-94-9 3,4-di-O-benzoyl-2,6-dideoxy-α-D-arabinopyranosyl fluoride 

Relevant academic research and scientific papers

Improvement in O -> C Glycoside Rearrangement Approach to C-Aryl Glycosides: Use of 1-O-Acetyl Sugar as Stable but Efficient Glycosyl Donor

1-O-Acetyl sugars serve as efficient glycosyl donor in the O -> C-glycoside rearrangement approach to C-aryl glycosides.Model study was carried out on three types of 2-deoxy-glycosyl acetates including amino sugar derivative.Comparison of the promoters, Cp2HfCl2-AgClO4, SnCl4, BF3*OEt2 is described.