145772-63-0

Upstream product

• 41546-30-9 β-L-arabinose 
• 172949-39-2 1,2-O-Isopropylidene-5-O-triphenylmethyl-α-L-xylofuranose 
• 114861-22-2 1,2-O-isopropylidene-α-L-xylofuranose 
• 609-06-3 L-xylose 
• 945621-29-4 (3aS,5S,6R,6aS)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 131156-47-3 (3aS,3bR,7aS,8aS)-2,2,5,5-tetramethyltetrahydro-3aH-[1,3]dioxolo[4',5':4,5]furo[3,2-d][1,3]dioxane 
• 166411-39-8 5-O-benzoyl-1,2-O-isopropylidene-7α-L-xylofuranose 
• 41546-31-0 L-xylose 
• 1333476-27-9 C₁₉H₂₂O₈ 
• 1333476-25-7 5-O-allyloxycarbonyl-1,2-O-isopropylidene-α-L-xylofuranose 
• 391201-57-3 [(3aS,5S,6R,6aS)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methanol 
• 528593-79-5 (3aS,5S,6R,6aS)-6-Benzyloxy-2,2-dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxole 

Downstream Products

• 29514-33-8 6,6,7,7-tetradehydro-6,7-dideoxy-α-D-gluco-heptofuranose 
• 29514-34-9 6,6,7,7-tetradehydro-6,7-dideoxy-β-L-ido-heptofuranose 
• 917222-29-8 Benzyl-[1-((3aS,5S,6R,6aS)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-meth-(E)-ylidene]-amine 
• 1333476-29-1 diethyl (5S)-(3-O-benzyl-1,2-O-isopropylidene-α-L-xylofuranos-5-C-yl)phoshonate 
• 1333476-30-4 diethyl (4S)-(1,3-di-O-acetyl-2-O-benzyl-α-L-threofuranos-4-yl)phosphonate 
• 1333476-31-5 diethyl (4S)-(1,3-di-O-acetyl-2-O-benzoyl-α-L-threofuranos-4-yl)phosphonate 
• 1333476-33-7 diethyl (4S)-[3-O-acetyl-2-O-benzoyl-1-deoxy-1-(thymin-1-yl)-α-L-threofuranos-4-yl]phosphonate 
• 1333476-34-8 diethyl (4S)-[3-O-acetyl-2-O-benzoyl-1-(4-N-benzoylcytosin-1-yl)-1-deoxy-α-L-threofuranos-4-yl]phosphonate 
• 528593-81-9 (2S,3S,4S,5R)-1-Benzyl-4-benzyloxy-2-methyl-piperidine-3,5-diol 
• 449729-69-5 1,6-dideoxy-L-nojirimycin 

Relevant academic research and scientific papers

Total Synthesis of 5-Hydroxygoniothalamin

The total synthesis of 5-hydroxygoniothalamin is achieved from commercially available l -xylose. The α,β-unsaturated-δ-lactone core is constructed in very good yield by utilizing one-carbon and two-carbon cis -Wittig olefinations and δ-lactonization using Yamaguchi conditions. Subsequent Grubbs cross-metathesis followed by desilylation results in 5-hydroxygoniothalamin.

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

First stereocontrolled synthesis and biological evaluation of 1,6-dideoxy-L-nojirimycin

The first synthesis of 1,6-dideoxy-L-nojirimycin in enantiomerically pure form has been achieved in nine steps from L-xylose in an overall yield of 15%. The biological activity of this compound as a glycosidase inhibitor provided useful information on str