104012-76-2

Upstream product

• 67-56-1 methanol 
• 128057-04-5 (3R,4S)-3-O-benzyl-4,5-O-isopropylidene-3,4,5-trihydroxypentanal 
• 128112-00-5 (2R,3S)-2-<3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 128057-00-1 (3R,4R)-3-O-benzyl-4,5-O-isopropylidene-3,4,5-trihydroxypentanal 
• 103795-36-4 (3S,4R)-3-O-benzyl-4,5-O-isopropylidene-3,4,5-trihydroxypentanal 
• 105386-66-1 methyl 3-O-benzyl-5-O-(t-butyldimethylsilyl)-2-deoxyribofuranoside 
• 128161-77-3 (2S,3R)-2-<2-O-benzyl-3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 128111-92-2 (2S,3R)-2-<3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 105454-48-6 3-O-Benzyl-2-deoxy-5-(triphenylmethyl)-D-erythro-pentofuranoside 
• 128111-95-5 (2R,3R)-2-<2-O-benzyl-3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 128111-94-4 (2R,3R)-2-<3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 128112-01-6 (2R,3S)-2-<2-O-benzyl-3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 

Downstream Products

• 103954-56-9 methyl 2-deoxy-3-O-benzyl-5-O-hexadecyl-α-D-erythro-pentofuranoside 
• 494211-90-4 (2R,3S,5S)-3-(benzyloxy)-5-methoxy-2-[4-(phenylthio)pent-4-enyl]tetrahydrofuran 
• 494211-87-9 (2R,3S,5S)-3-(benzyloxy)-5-methoxy-2-[3-(phenylthio)but-3-enyl]tetrahydrofuran 
• 494212-30-5 (1R,6R,7S)-7-(benzyloxy)-9-oxabicyclo[4.2.1]nonan-3-one 
• 494211-89-1 (2R,3S,5S)-2-allyl-3-(benzyloxy)-5-methoxytetrahydrofuran 
• 494211-86-8 (2R,3S,5S)-3-(benzyloxy)-5-methoxy-2-vinyltetrahydrofuran 
• 161606-70-8 Methyl 3-O-benzyl-2-deoxy-5-α-D-erythro-pentodialdo-1,4-furanoside 
• 51255-17-5 1-O-methyl-α-2-deoxy-D-erythro-pentofuranose 

Relevant academic research and scientific papers

Sugar-modified foldamers as conformationally defined and biologically distinct glycopeptide mimics

To fold or not to fold? It is shown that attached sugars play a defining role in the conformations adopted by a pair of novel SAA-derived foldamers in water and that these differences are reflected in the contrasting interactions of these glycofoldamers with various biological targets. C green, O red, N blue, H gray; yellow oval=mannose. Copyright

Stereoselectivity of Addition of Organometallic Reagents to Pentodialdo-1,4-furanoses: Synthesis of L-Axenose and D-Evermicose from a Common Intermediate

The additions of organometallic reagents to two pentodialdo-1,4-furanosides (methyl 3-O-benzyl-2-deoxy-α-D-erythro-pentofuranoside and its β-anomer) were carried out under a variety of experimental conditions.Methylmagnesium halides, methyllithium, methyl

Chemistry of L-Ascorbic and D-Isoascorbic Acids. An Efficient Synthesis of 2-Deoxypentofuranoses

L-Ascorbic and D-isoascorbic acids have been converted to methyl 3-O-benzyl-2-deoxypentofuranosides.The synthetic routes are enantiospecific, efficient, and economic and proceed in high yields.