65462-15-9

Upstream product

• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 68354-70-1 3-O-benzyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 110237-79-1 5-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 1333476-18-8 methyl 5-O-benzoyl-β-L-arabinoside 
• 6893-72-7 5-O-benzoyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 3795-69-5 methyl β-L-arabinofuranoside 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 168103-01-3 3-O-benzyl-1,2-O-isopropylidene-5-O-(tert-butyldiphenylsilyl)-β-L-arabinofuranose 
• 103763-14-0 (3aR,5S,6S,6aR)-5-{[(tert-butyldiphenylsilyl)oxy]methyl}-2,2-dimethyltetrahydro-2H-furo[2,3-d][1,3]dioxol-6-ol 
• 100-44-7 benzyl chloride 
• 65451-98-1 3-O-benzyl-1,2:5,6-di-O-isopropylidene-α-D-galactofuranose 
• 2774-28-9 3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-erythro-hex-3-enofuranose 
• 10368-86-2 1,2:5,6-di-O-isopropylidene-α-D-galactofuranose 
• 65434-49-3 3-O-benzyl-1,2-O-isopropylidene-α-D-galactofuranose 

Downstream Products

• 65434-50-6 3-O-benzyl-5,6-dideoxy-6-C-(n-hexyl)-1,2-O-isopropylidene-β-L-arabino-hex-5-enofuranose 
• 599196-25-5 C₁₅⁽¹³⁾CH₂₀O₄ 
• 599196-29-9 C₁₅⁽¹³⁾CH₂₀O₅ 
• 599196-31-3 C₁₅⁽¹³⁾CH₂₂O₆ 
• 98855-09-5 3-O-benzyl-5-deoxy-5-C-(n-heptyl)-1,2-O-isopropylidene-β-L-arabinofuranose 
• 1234573-87-5 3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone 
• 1361026-55-2 C₂₀H₁₈O₄ 
• 1457973-59-9 C₂₀H₂₀O₄ 
• 18439-43-5 3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-D-gluco-pentafuranose 
• 20715-20-2 3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-D-xylo-pent-5-ulo-furanose 
• 1457973-40-8 3-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-β-L-ido-pentofuranose 
• 1361026-56-3 3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone 
• 899436-70-5 5-O-benzoyl-3-O-benzyl-1,2-isopropylidene-5-C-phenyl-α-D-gluco-pentofuranose 
• 18439-42-4 3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-L-ido-pentofuranose 

Relevant academic research and scientific papers

Divergent total synthesis of crassalactones B and C and evaluation of their antiproliferative activity

A divergent total synthesis of cytotoxic natural products (+)-crassalactones B (2) and C (3) has been achieved by utilizing diacetone d-glucose (4) as a chiral precursor. The key steps of the synthesis of both targets 2 and 3 were a stereo-selective addit

Heteroannelated and 7-deoxygenated goniofufurone mimics with antitumour activity: Design, synthesis and preliminary SAR studies

Cytotoxic (+)-goniofufurone mimic such as benzoxepane 2 was preferentially formed after the treatment of 7-O-benzoyl-5-O-benzyl (+)-goniofufurone derivative 6 with titanium(IV) fluoride. However, the corresponding 7-epimer 5 (derivative of 7-epi-goniofufu

Tetrofuranose nucleoside phosphonic acids: Synthesis and properties

New isoelectronic, non-isosteric phosphonate analogues of nucleoside 5'-phosphates featuring the phosphorus moiety directly attached on the sugar ring in the C4' position are described. The analogues were synthesised by a nucleosidation reaction from tetr

Practical synthesis of [1-13C]- and [6-13C]-D-galactose

The chemical synthesis of 13C-labeled D-galactose as useful molecular probes for studying the conformation of oligosaccharides attached to proteins was performed. The method for synthesizing the title labeled compounds was newly developed via t

The Raction of Acetyliron 5-C5H5)Fe(CO)(PPh3)(COCH3)> with Sugar Aldehydes. New Synthesis of Deoxysugars

Aldol reactions of sugar aldehydes (5-13) with enolate 2 of racemic and both enantiomeric forms of acetyliron were investigated.The steric course of reactions depended strongly on the counterions used.High stereocontrol was achieved with the following cat