34370-91-7

Basic information

• Product Name: 3-O-Benzyl-1-O,2-O-isopropylidene-β-L-lyxofuranose
• Synonyms: 3-O-Benzyl-1-O,2-O-isopropylidene-β-L-lyxofuranose;1,2-O-(1-Methylethylidene)-3-O-(phenylmethyl)-beta-L-lyxofuranose;3-O-Benzyl-1,2-O-isopropylidene-b-L-lyxofuranose
• CAS NO: 34370-91-7
• Molecular Formula: C₁₅H₂₀O₅
• Molecular Weight: 280.3163
• Mol File: 34370-91-7.mol
• Article Data: 53

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-O-Benzyl-1-O,2-O-isopropylidene-β-L-lyxofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-Benzyl-1-O,2-O-isopropylidene-β-L-lyxofuranose(34370-91-7)
• EPA Substance Registry System: 3-O-Benzyl-1-O,2-O-isopropylidene-β-L-lyxofuranose(34370-91-7)

Safety Data

• Hazardous Substances Data: 34370-91-7(Hazardous Substances Data)

Upstream product

• 167500-61-0 3-O-benzyl-5-O-(tert-butyldimethylsilyl)-1,2-O-isopropylidene-α-D-xylofuranose 
• 100-39-0 benzyl bromide 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 40429-53-6 5-O-p-toluenesulfonyl-3-O-benzyl-1,2-O-isopropylidene-β-D-arabinofuranose 
• 126308-97-2 (3aR,5R,6S,6aR)-6-Benzyloxy-5-(3,4-dimethoxy-benzyloxymethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole 
• 42926-89-6 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose 
• 29581-48-4 O-benzyl-1,2-di-O-isopropylidene-5-O-(p-toluenesulfonyl)-α-D-xylofuranose 
• 168608-39-7 (3S,4S,5R)-5-(((tert-butyldiphenylsilyl)oxy)methyl)tetrahydrofuran-2,3,4-triol 
• 10323-20-3 D-Arabinose 
• 7151-04-4 5-O-benzoyl-D-arabinose diethyl dithioacetal 
• 40429-51-4 1,2-O-isopropylidene-5-O-toluene-p-sulphonyl-β-D-arabinofuranose 
• 100-44-7 benzyl chloride 
• 114738-04-4 (3aS,5R,6R,6aS)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 168103-00-2 (((3aS,5R,6R,6aS)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methoxy)(tert-butyl)diphenylsilane 

Downstream Products

• 89747-32-0 3-O-benzyl-1,2-O-isopropylidene-5-O-sulfamyl-β-D-arabinofuranose 
• 117661-89-9 3-O-benzyl-1,2-O-isopropylidene-5-O-trifluoromethanesulphonyl-α-D-xylofuranose 
• 79083-39-9 1-O-methyl 3,5-di-O-benzyl β(D)xylo-pentoaldofuranose 
• 79083-38-8 1-O-methyl 3,5-di-O-benzyl α(D)xylo-pentoaldofuranose 
• 87060-33-1 (2R,3R)-2-Benzyloxy-4-octadecyloxy-butane-1,3-diol 
• 87060-34-2 (2R,3R)-3-Benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-1-octadecyloxy-butan-2-ol 
• 87060-35-3 (2R,3R)-2,3-Bis-benzyloxy-4-octadecyloxy-butan-1-ol 
• 87060-37-5 C₄₁H₇₀NO₇P 
• 74644-88-5 2,3-trans-3,4-trans-3,4-dihydroxy-L-proline 
• 131053-22-0 5-deoxy-1,2-O-(1-isopropylidene)-3-O-benzyl-α-D-xylohexofuranonitrile 
• 131053-15-1 5-azido-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-D-xylofuranose 
• 100937-52-8 1,4-dideoxy-1,4-imino-D-arabitol 
• 131102-04-0 methyl 3-O-benzyl-2,5-dideoxy-2,5-imino-β-D-lyxofuranoside 
• 131053-18-4 methyl 3-O-benzyl-2,5-dideoxy-2,5-imino-α-D-lyxofuranoside 

Relevant articles and documents

Synthesis of Benz-Fused Azoles via C-Heteroatom Coupling Reactions Catalyzed by Cu(I) in the Presence of Glycosyltriazole Ligands

Glycosyl triazoles are conveniently accessible and contain multiple metal-binding units that may assist in metal-mediated catalysis. Azide derivatives of d-glucose have been converted to their respective aryltriazoles and screened as ligands for the synthesis of 2-substituted benz-fused azoles and benzimidazoquinazolinones by Cu-catalyzed intramolecular Ullmann type C-heteroatom coupling. Good to excellent yields for a variety of benz-fused heterocyles were obtained for this readily accessible catalytic system.

Visible-Light-Mediated, Chemo- and Stereoselective Radical Process for the Synthesis of C-Glycoamino Acids

An approach for efficient synthesis of C-glycosyl amino acids is described. Different from typical photoredox-catalyzed reactions of imines, the new process follows a pathway in which α-imino esters serve as electrophiles in chemoselective addition reactions with nucleophilic glycosyl radicals. The process is highlighted by the mild nature of the reaction conditions, the highly stereoselectivity attending C-C bond formation, and its applicability to C-glycosylations using both armed and disarmed pentose and hexose derivatives.

Furan glucosyl triazole type compound and preparation method and bactericide thereof

The invention relates to the field of bactericidal compounds, in particular to a furan glucosyl triazole type compound and a preparation and a bactericide thereof. The molecular formula of the furan glucosyl triazole type compound is shown in the following description, wherein R1 is methyl or benzyl, and R2 are phenyl and derivative of the phenyl or ethyl derivatives. Based on structural characteristics of the substrate fructose-6-phosphate and an ISOM catalytic hypothesis mechanism, the inventor adopts a five-membered furan glucose derivative with a similar structure as a basic skeleton, introduces an effective active group triazole structure of pesticides, designs a series of novel furan glucosyl triazole type compounds for the first time, studies the biological activities of the furan glucosyl triazole type compound, examines structure-activity relationships of the furan glucosyl triazole type compound, and lays the foundation for selecting better inhibitors.