130931-97-4

Basic information

• Product Name: (-)-(3R,4S)-4-benzyloxytetrahydrofuran-3-ol
• Synonyms: (-)-(3R,4S)-4-benzyloxytetrahydrofuran-3-ol
• CAS NO: 130931-97-4
• Molecular Weight: 194.23
• Mol File: 130931-97-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (-)-(3R,4S)-4-benzyloxytetrahydrofuran-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(3R,4S)-4-benzyloxytetrahydrofuran-3-ol(130931-97-4)
• EPA Substance Registry System: (-)-(3R,4S)-4-benzyloxytetrahydrofuran-3-ol(130931-97-4)

Safety Data

• Hazardous Substances Data: 130931-97-4(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 4358-64-9 cis-1,4-anhydroerythritol 
• 199122-72-0 (3S,4R)-3-Benzyloxy-4-[(R)-methoxy-((1R,2R,3S,4S)-3-methyl-bicyclo[2.2.1]hept-5-en-2-yl)-methoxy]-tetrahydro-furan 
• 130871-07-7 Acetic acid (3R,4S)-4-benzyloxy-tetrahydro-furan-3-yl ester 

Downstream Products

• 183387-05-5 4-Nitro-benzoic acid (3S,4S)-4-benzyloxy-tetrahydro-furan-3-yl ester 
• 183387-09-9 9-((3S,4R)-4-Benzyloxy-tetrahydro-furan-3-yl)-9H-purin-6-ylamine 
• 183387-10-2 9-((3R,4R)-4-Benzyloxy-tetrahydro-furan-3-yl)-9H-purin-6-ylamine 
• 183387-07-7 (3S,4S)-4-benzyloxy-tetrahydro-furan-3-ol 
• 153922-95-3 Methanesulfonic acid (3R,4S)-4-benzyloxy-tetrahydro-furan-3-yl ester 

Relevant articles and documents

Dimethyltin Dichloride Catalyzed Regioselective Alkylation of cis-1,2-Diols at Room Temperature

Here, we have developed a mild and general method for the regioselective installation of benzyl, allyl, para-methoxybenzyl and naphthyl groups on cis-1,2-diols. The optimized method operates at room temperature using dimethyltin dichloride as catalyst and

Asymmetric desymmetrization of saturated and unsaturated meso-1,2-diols

An asymmetric desymmetrization of saturated and unsaturated cyclic and acyclic meso-1,2-diols has been developed from the ene acetals, prepared from the norbornene carboxyaldehyde and meso-1,2-diols. The intramolecular haloetherification of the ene acetals as a key step afforded 8-membered acetals in a stereoselective manner just by the reaction of norbornene olefin even when the ene acetals from unsaturated meso-1,2-diols having olefins in the same molecule were used. Subsequent reductive elimination, followed by protecting the hydroxy group and transacetalization, gave optically active 1,2-diol derivatives and the starting ene acetals in good yields. (C) 2000 Elsevier Science Ltd.

Highly enantioselective asymmetrization of meso-1,2-diols through a novel and efficient reaction cycle

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