101703-83-7

Basic information

• Product Name: 1,3,4-tribenzyloxy-D-erythritol
• Synonyms: 1,3,4-tribenzyloxy-D-erythritol
• CAS NO: 101703-83-7
• Molecular Weight: 392.495
• Mol File: 101703-83-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3,4-tribenzyloxy-D-erythritol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4-tribenzyloxy-D-erythritol(101703-83-7)
• EPA Substance Registry System: 1,3,4-tribenzyloxy-D-erythritol(101703-83-7)

Safety Data

• Hazardous Substances Data: 101703-83-7(Hazardous Substances Data)

Upstream product

• 101703-81-5 Benzoic acid (1R,2R,3S)-2,3-bis-benzyloxy-1-benzyloxymethyl-4-oxo-butyl ester 
• 16838-89-4 2,3,5-tri-O-benzyl-D-arabinose 
• 4645-59-4 4-O-Benzoyl-2,3,5-tri-O-benzyl-D-arabinose-diaethyldithioacetal 
• 114184-95-1 (R)-3,4-Dihydroxy-5-((R)-2-phenyl-[1,3]dioxolan-4-yl)-5H-furan-2-one 
• 114184-96-2 ethyl (2R,3R)-3,4,-O-benzylidene-2,3,4-trihydroxybutanoate 
• 100-52-7 benzaldehyde 
• 100-39-0 benzyl bromide 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 333363-59-0 (4R,5S)-4,5-Bis-benzyloxymethyl-2-hept-1-ynyl-[1,3]dioxolane 
• 69010-01-1 (2R*,3S*)-1,4-bis(benzyloxy)butane-2,3-diol 
• 199122-82-2 (1S,4R,5R,6S)-5-[(R)-((1R,2S)-2,3-Bis-benzyloxy-1-benzyloxymethyl-propoxy)-methoxy-methyl]-6-methyl-bicyclo[2.2.1]hept-2-ene 
• 114185-02-3 (2S,3R)-1,2-epoxy-3,4-bis(benzyloxy)butane 
• 100-51-6 benzyl alcohol 
• 114185-01-2 (2R,3S)-3,4-di-O-benzyl-1,2-O-benzylidenebutane-1,2,3,4-tetrol 

Downstream Products

• 101703-86-0 2-Amino-9-((1R,2S)-2,3-bis-benzyloxy-1-benzyloxymethyl-propoxymethyl)-1,9-dihydro-purin-6-one 
• 101703-85-9 9-((1R,2S)-2,3-Bis-benzyloxy-1-benzyloxymethyl-propoxymethyl)-6-chloro-9H-purin-2-ylamine 
• 117486-37-0 ethyl 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxylate 
• 117486-38-1 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxamide 
• 101703-84-8 2R-chloromethoxy-1,3S,4-tribenzyloxybutane 

Relevant articles and documents

Desymmetrization of meso-1,2-diols via chiral Lewis acid-mediated ring-cleavage of 1,3-dioxolane derivatives

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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.

The chemistry of L-ascorbic and D-isoascorbic acids. I. The preparation of chiral butanetriols and -tetrols

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