250696-90-3

Upstream product

• 1774-47-6 trimethylsulfoxonium iodide 
• 89956-14-9 [3-(2-Benzyloxyethyl)oxiran-2-yl]methanol 
• 250696-85-6 Benzoic acid (3aR,5R,6R,6aR)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 250696-99-2 Benzoic acid (3aR,5R,6R,6aR)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-(imidazole-1-carbothioyloxy)-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 250697-00-8 Benzoic acid (2R,3R,4S)-2-(2-benzyloxy-ethyl)-4-(imidazole-1-carbothioyloxy)-tetrahydro-furan-3-yl ester 
• 250696-86-7 3-O-benzoyl-6-O-(tert-butyldimethylsilyl)-5-deoxy-1,2-O-isopropylidene-α-D-ribo-hexofuranose 
• 250696-87-8 6-O-benzyl-3-O-benzoyl-5-deoxy-1,2-O-isopropylidene-D-allofuranose 
• 250696-88-9 6-O-benzyl-3-O-benzoyl-1,5-dideoxy-D-allofuranose 
• 2595-05-3 Diacetone D-glucose 
• 113808-25-6 3-O-benzoyloxy-5-deoxy-1,2-O-isopropylidene-α-D-ribohexofuranose 
• 31795-13-8 3-O-benzoyl-1,2-O-isopropylidene-α-D-allofuranose 
• 29474-73-5 (+)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranos-3-yl benzoate 
• 250696-89-0 Benzoic acid (2R,3S)-2-(2-benzyloxy-ethyl)-tetrahydro-furan-3-yl ester 

Downstream Products

• 250696-92-5 9-[(2R,3R)-2-(2-Benzyloxy-ethyl)-tetrahydro-furan-3-yl]-9H-purin-6-ylamine 
• 250696-93-6 1-[(2R,3R)-2-(2-Benzyloxy-ethyl)-tetrahydro-furan-3-yl]-5-methyl-1H-pyrimidine-2,4-dione 
• 250696-94-7 1-[(2R,3R)-2-(2-Benzyloxy-ethyl)-tetrahydro-furan-3-yl]-1H-pyrimidine-2,4-dione 
• 250696-91-4 6-O-benzyl-3-O-mesyl-1,2,5-trideoxy-D-allofuranose 

Relevant academic research and scientific papers

Synthesis of diastereomerically and enantiomerically pure 2,3-disubstituted tetrahydrofurans using a sulfoxonium ylide

Nucleophilic substitution reactions of 2,3-epoxy alcohols, easily prepared via Sharpless asymmetric epoxidation chemistry, offer access to a wide variety of enantiomerically pure compounds. In this communication, we describe the use of a Payne rearrangement to control regioselectivity in the ring-opening of a series of 2,3-epoxy alcohols with dimethylsulfoxonium methylide to yield diastereomerically and/or enantiomerically pure disubstituted tetrahydrofuran rings. The factors influencing the success and substitution pattern of the THF ring products are discussed, including steric, electronic, and solvent effects. Copyright

Homologues of isomeric dideoxynucleosides as potential antiviral agents: Synthesis of isodideoxy-nucleosides with a furanethanol sugar moiety

The synthesis of a homologues series of compounds related to (R, S)- isodideoxynucleosides has been completed by coupling a variety of natural purine and pyrimidine bases with a modified sugar intermediate. This sugar precursor was prepared regiospecifica