78038-33-2

Upstream product

• 77977-38-9 5-O-benzyl-3-deoxy-4-O-mesyl-D-pentitol 
• 77977-37-8 5-O-benzyl-3-deoxy-1,2-O-isopropylidene-4-O-(methylsulfonyl)-D-pentitol 
• 163956-65-8 methyl 5-O-benzyl-3-deoxy-L-erythro-pentofuranoside 
• 32785-98-1 3-deoxy-1,2:5,6-di-O-isopropylidene-β-D-lyxo-hexose 
• 114861-23-3 3-deoxy-1,2-O-isopropylidene-α-L-erythro-pentofuranose 
• 114861-24-4 3-deoxy-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-L-xylofuranose 
• 4005-46-3 3-deoxy-1,2-O-isopropylidene-α-L-glucose 
• 4613-68-7 (3aS,5R,6aS)-2,2-Dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 
• 100638-80-0 1,2:5,6-di-O-isopropylidene-3-O-(methylthio)thiocarbonyl-β-D-idose 
• 38166-60-8 1,2:5,6-di-O-isopropylidene-α-L-glucofuranoside 

Downstream Products

• 77977-39-0 (2R)-benzyloxymethyl-4oxo-tetrahydrofuran 
• 72369-98-3 (2R,4S)-4-amino-2-(benzyloxymethyl)tetrahydrofuran-4-carboxylic acid 
• 72369-98-3 (3S,5R)-3-Amino-5-benzyloxymethyl-tetrahydro-furan-3-carboxylic acid 
• 81275-25-4 (2R,4R)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran 
• 81275-26-5 (2R,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran 
• 72369-96-1 (2S)-benzyloxymethyl-4-oxo-tetrahydrofuran 
• 72402-17-6 (2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran 
• 72369-97-2 (2S,4R)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran 
• 72369-98-3 (3R,5S)-3-Amino-5-benzyloxymethyl-tetrahydro-furan-3-carboxylic acid 
• 72369-98-3 (2S,4S)-4-amino-2-(benzyloxymethyl)tetrahydrofuran-4-carboxilic acid 
• 142941-41-1 (2R,4S)-2-<(benzyloxy)methyl>-4-<(methylsulfonyl)oxy>tetrahydrofuran 
• 127682-75-1 IsoddA 
• 132813-69-5 (3'R,5'R)-4-amino-1-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>-5-methylpyrimidine-2(1H)-one 
• 132813-68-4 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>-pyrimidine-2,4(1H,3H)-dione 

Relevant academic research and scientific papers

Enantiospecific Synthesis of 3'-Hetero-dideoxy Nucleoside Analogues as Potential Anti-HIV Agents

Two series of analogues of 2',3'-dideoxy carbocyclic nucleosides, in which the 3'-carbon atom is replaced by either an oxygen or a sulfur atom, have been prepared enantiospecifically from diacetone-L-glucose and diacetone-D-glucose respectively.Within eac

SYNTHESIS OF FOUR STEREOISOMERS OF 4-AMINO-2-(HYDROXY-METHYL)TETRAHYDROFURAN-4-CARBOXYLIC ACID

The 5-benzyl ether, 15, of a 1,2,,4,5-pentanetetrol of known 2S configuration was made by a multistep synthesis from D-ribose.Ring-closure of the 1-O-otosyl derivative, 17, with retention of configuration, followed by oxidation, gave the 2S enantiomer, 22