128461-94-9

Upstream product

• 136459-89-7 acetyl 3,4-di-O-benzoyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 106988-66-3 C₂₀H₂₀O₆ 
• 32476-34-9 Methyl 3,4-di-O-benzoyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 88999-65-9 C₂₂H₂₂O₇ 

Downstream Products

• 128462-00-0 C₃₁H₂₈O₇ 
• 128461-99-4 C₃₁H₂₈O₇ 
• 128462-02-2 C₃₇H₃₄O₉ 
• 128461-97-2 C₃₀H₂₆O₆ 
• 128461-95-0 C₃₀H₂₆O₆ 
• 128461-96-1 C₃₀H₂₆O₆ 
• 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 

Relevant academic research and scientific papers

Stereocontrolled halofluorination of glycals with silicon tetrafluoride, leading to a facile synthesis of glycosyl fluorides

Bromofluorination of glycals was carried out with SiF4, 1,3-dibromo-5,5-dimethylhydantoin (DBH), and H2O in 1,4-dioxane in the presence of HMPA to give bromofluoro sugars in good yields with good selectivities. Subsequent debrominati

Synthetic Study toward Vineomycins. Synthesis of C-Aryl Glycoside Sector via Cp2HfCl2-AgClO4-Promoted Tactics

Regio- and stereo-controlled formation of C-aryl β-D-olivoside linkage is achieved by the reaction of naphthol or anthrol derivatives with D-olivosyl fluoride.The reaction is efficiently promoted by Cp2HfCl2-AgClO4 and the bond formation occurs selectivit