320592-10-7

Upstream product

• 100-39-0 benzyl bromide 
• 172949-42-7 (3aS,5S,6S,6aS)-5-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,2-d][1,3]dioxol-6-ol 
• 41546-31-0 L-xylose 
• 144490-03-9 1,2,3,5-tetra-O-acetyl-β-L-ribofuranose 
• 1439372-63-0 ((3aS,5S,6S,6aS)-6-acetoxy-2,2-dimethyltetrahydrofuro[3,2-d][1,3]dioxol-5-yl)methyl acetate 
• 171721-11-2 5-O-benzoyl-1,2-O-isopropylidene-α-L-ribofuranose 
• 100-44-7 benzyl chloride 
• 320592-05-0 5-O-(p-chlorobenzoyl)-1,2-O-isopropylidene-α-L-ribofuranose 
• 320591-97-7 5-O-(p-chlorobenzoyl)-1,2-O-isopropylidene-α-L-xylofuranose 
• 320592-02-7 5-O-(p-chlorobenzoyl)-1,2-O-isopropylidene-α-L-erythro-pentofuranos-3-ulose 
• 114861-22-2 1,2-O-isopropylidene-α-L-xylofuranose 

Downstream Products

• 320592-15-2 1,4-anhydro-3,5-di-O-benzyl-2-deoxy-L-erythro-pent-1-enitol 
• 320592-25-4 3-fluoro-4-(β-L-glyceropentofuran-3-ulos-1-yl)aniline 
• 320592-21-0 4-(5-((benzyloxy)methyl)-4-(benzyloxy)-2,5-dihydro-β-L-furan-2-yl)-3-fluoroaniline 
• 1439372-97-0 (1R,2S,3R,8aR)-2-(benzyloxy)-3-(benzyloxymethyl)-1,2,3,5,6,8a-hexahydroindolizin-1-ol 
• 1439372-80-1 (2S,3R,4R,E)-1,3-bis(benzyloxy)-5-((R)-pent-4-en-2-ylamino)-7-phenylhept-6-ene-2,4-diol 
• 1439372-89-0 (2S,3R,4R,E)-1,3-bis(benzyloxy)-5-(but-3-enylamino)-7-phenylhept-6-ene-2,4-diol 
• 1439372-82-3 (2R,3R,4S,5R)-4-(benzyloxy)-5-(benzyloxymethyl)-1-((R)-pent-4-en-2-yl)-2-styrylpyrrolidin-3-ol 
• 1439372-93-6 (2R,3R,4S,5R)-4-(benzyloxy)-5-(benzyloxymethyl)-1-(but-3-enyl)-2-styrylpyrrolidin-3-ol 
• 1439372-84-5 (1R,2S,3R,5R,8aR)-2-(benzyloxy)-3-(benzyloxymethyl)-5-methyl-1,2,3,5,6,8a-hexahydroindolizin-1-ol 

Relevant academic research and scientific papers

Synthesis of a 3′-Fluoro-3′-deoxytetrose Adenine Phosphonate

A new synthetic route to a 3′-fluoro-3′-deoxytetrose adenine phosphonate has been developed. The synthesis starts from l-xylose and key steps include the stereospecific introduction of the phosphonomethoxy group and adenine. In addition, a regioselective

Concise synthesis of (-)-steviamine and analogues and their glycosidase inhibitory activities

A concise synthesis of (-)-steviamine is reported along with the synthesis of its analogues 10-nor-steviamine, 10-nor-ent-steviamine and 5-epi-ent-steviamine. These compounds were tested against twelve glycosidases (at 143 μg mL-1 concentrations) and were found to have in general poor inhibitory activity against most enzymes. The 10-nor analogues however, showed 50-54% inhibition of α-l-rhamnosidase from Penicillium decumbens while one of these, 10-nor-steviamine, showed 51% inhibition of N-acetyl-β-d-glucosaminidase (from Jack bean) at the same concentration (760 μM). This journal is The Royal Society of Chemistry 2013.