72369-95-0

Upstream product

• 78038-32-1 5-O-benzyl-3-deoxy-D-pentitol 
• 78038-30-9 methyl 5-O-benzoyl-2,3-di-O-methyl-D-xylofuranoside 
• 81227-14-7 5-O-benzyl-2,3-di-O-methyl-D-xylofuranose 
• 3396-71-2 3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 
• 116306-89-9 (3αR,5S,6αR)-5-(benzyloxymethyl)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole 
• 72369-92-7 5-O-benzyl-3-deoxy-D-glycero-2-pentulose 
• 81227-15-8 5-O-benzoyl-3-deoxy-2-O-methyl-D-glycero-pent-2-enofuranose 
• 100-39-0 benzyl bromide 

Downstream Products

• 191600-58-5 ((3S,5S)-5-Benzyloxymethyl-tetrahydro-furan-3-yl)-[6-chloro-5-(2,2-diethoxy-ethyl)-pyrimidin-4-yl]-amine 
• 191600-62-1 2-amino-7-[(2S,4S)-(2-benzyloxymethyl)-tetrahydrofuran-4-yl]-4-chloropyrrolo[2,3-d]pyrimidine 
• 191600-64-3 2-amino-7-[(2S,4S)-(2-benzyloxymethyl)-tetrahydrofuran-4-yl]pyrrolo[2,3-d]pyrimidin-4(3H)-one 
• 191600-59-6 7-[(2S,4S)-(2-benzyloxymethyl)-tetrahydrofuran-4-yl]-4-chloropyrrolo[2,3-d]pyrimidine 
• 191600-60-9 4-amino-7-[(2S,4S)-(2-benzyloxymethyl)-tetrahydrofuran-4-yl]pyrrolo[2,3-d]pyrimidine 
• 191600-61-0 7-[(2S,4S)-(2-benzyloxymethyl)-tetrahydrofuran-4-yl]pyrrolo[2,3-d]pyrimidin-4(3H)-one 
• 191600-56-3 (2S,4S)-4-azido-2-(benzyloxymethyl)tetrahydrofuran 
• 191600-57-4 (2S,4S)-4-amino-2-(benzyloxymethyl)tetrahydrofuran 
• 72369-98-3 (2S,4S)-4-amino-2-(benzyloxymethyl)tetrahydrofuran-4-carboxilic acid 
• 72369-98-3 (3R,5S)-3-Amino-5-benzyloxymethyl-tetrahydro-furan-3-carboxylic acid 
• 72369-97-2 (2S,4R)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran 
• 72402-17-6 (2S,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran 
• 72369-96-1 (2S)-benzyloxymethyl-4-oxo-tetrahydrofuran 
• 81275-26-5 (2R,4S)-2-benzyloxymethyl-4-C-(spiro-5-hydantoin)tetrahydrofuran 

Relevant academic research and scientific papers

Synthesis of some pyrrolo[2,3-

The pynolo[2,3-d]pyrimidine isodideoxynucleosides 7,8, and 9, related to the (S.S)-enantiomers of iso-2',3'-dideoxy-adenosine, -inosine and -guanosine respectively, have been prepared from D-xylose. Copyright

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