114861-37-9

Basic information

• Product Name: 3-deoxy-5-O-(phenylmethyl)-α-L-xylofuranose
• Synonyms: 3-deoxy-5-O-(phenylmethyl)-α-L-xylofuranose
• CAS NO: 114861-37-9
• Molecular Weight: 224.257
• Mol File: 114861-37-9.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 3-deoxy-5-O-(phenylmethyl)-α-L-xylofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-deoxy-5-O-(phenylmethyl)-α-L-xylofuranose(114861-37-9)
• EPA Substance Registry System: 3-deoxy-5-O-(phenylmethyl)-α-L-xylofuranose(114861-37-9)

Safety Data

• Hazardous Substances Data: 114861-37-9(Hazardous Substances Data)

Upstream product

• 532-20-7 α-D-xylofuranose 
• 20590-53-8 1,2-O-isopropylidene-5-O-trityl-α-D-xylofuranose 
• 41546-31-0 L-xylose 
• 114861-22-2 1,2-O-isopropylidene-α-L-xylofuranose 
• 114861-15-3 Thiocarbonic acid O-[(3aS,5S,6R,6aS)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl] ester O-phenyl ester 
• 220827-73-6 5-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-α-L-xylofuranose 
• 106799-16-0 tert-Butyl-((3aS,5R,6aS)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethoxy)-diphenyl-silane 
• 114861-23-3 3-deoxy-1,2-O-isopropylidene-α-L-erythro-pentofuranose 
• 100-39-0 benzyl bromide 
• 114861-24-4 3-deoxy-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-L-xylofuranose 
• 3396-71-2 3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 
• 116306-89-9 (3αR,5S,6αR)-5-(benzyloxymethyl)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole 
• 41107-64-6 Acetic acid (3aR,5R,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester 
• 14260-66-3 ((3αR,5S,6αR)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol 

Downstream Products

• 72369-93-8 (2S,4R)-1-benzyloxy-2,4,5-trihydroxypentane 
• 142941-57-9 1-[(3R,5R)-5-(hydroxymethyl)tetrahydrothiophen-3-yl]pyrimidine-2,4-dione 
• 142941-59-1 (3'R,5')-1-<5'-(hydroxymethyl)tetrahydro-3'-thienyl>-5-methylpyrimidine-2,4(1H,3H)-dione 
• 142941-51-3 (2R,4S)-2-<(benzyloxy)methyl>-4-<(methylsulfonyl)oxy>tetrahydrothiophene 
• 142952-69-0 6-amino-9-[(3R,5R)-5-(hydroxymethyl)tetrahydrothiophen-3-yl]purine 
• 142941-49-9 (2R,4S)-2-benzoyloxy-5-(benzyloxy)pentane-1,4-diol 
• 142941-60-4 (2R,4R)-4-(2'-amino-6'-chloro-9'H-purin-9'-yl)tetrahydrothiophene-2-methanol 
• 132813-67-3 (2R,4S)-4-benzoyloxy-2-<(benzyloxy)methyl>tetrahydrothiophene 
• 142941-53-5 (3'R,5'R)-4-amino-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>pyrimidin-2(1H)-one 
• 142941-52-4 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>pyrimidine-2,4-(1H,3H)-dione 
• 142941-46-6 methyl 2-O-benzoyl-5-O-benzyl-3-deoxy-D-erythropentofuranoside 
• 142941-54-6 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>5-methylpyrimidine-2,4-(1H,3H)-dione 
• 142941-55-7 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>-9H-purin-6-amine 
• 142941-56-8 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>-6-chloro-9H-purin-6-amine 

Relevant articles and documents

METHODS FOR TREATING ARENAVIRIDAE AND CORONAVIRIDAE VIRUS INFECTIONS

Provided are methods for treating Arenaviridae and Coronaviridae virus infections by administering nucleosides and prodrugs thereof, of Formula I: wherein the 1′ position of the nucleoside sugar is substituted. The compounds, compositions, and methods provided are particularly useful for the treatment of Lassa virus and Junin virus infections.

A general strategy for the formal synthesis of (-)-trans-kumausyne and total synthesis of (5R)-Hagen's gland lactones from diacetone-D-glucose

A general strategy for the formal synthesis of (-)-trans-kumausyne 1 via the bicyclic lactone (3aR,5R,6aR)-4 and total synthesis of (5R)-Hagen's gland lactones 2 and 3 via bicyclic lactone (3aR,5S,6aR)-5 starting from diacetone-D-glucose 6 is described. Syntheses of 4 and 5 were achieved by Wittig olefination-lactonization-Michael addition of the corresponding lactols 16 and 17, respectively. Copyright (C) 2000 Elsevier Science Ltd.

Stereocontrolled synthesis of all stereoisomers of the proposed flavolipin

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