80524-17-0

Upstream product

• 532-32-1 sodium benzoate 
• 81668-68-0 Toluene-4-sulfonic acid (2S,3S,4R)-3-hydroxy-2-methoxy-tetrahydro-pyran-4-yl ester 
• 109606-19-1 Methyl-2,3-anhydro-β-L-ribopyranosid 
• 20679-23-6 trans-3,4-Epoxy-2-methoxy-tetrahydropyran 
• 65-85-0 benzoic acid 
• 98-88-4 benzoyl chloride 
• 75754-41-5 4-desoxy-1,2-O-isopropylidene-β-D,L-threo-pentopyranose 
• 67-56-1 methanol 
• 80524-16-9 O-benzoyl-3-desoxy-4-O-isopropylidene-1,2-β-DL-threo-pentopyranose 

Downstream Products

• 92050-98-1 methyl-3-O-benzoyl-4-desoxy-2-O-methoxymethyl-β-D,L-threo-pentopyranoside 
• 81686-58-0 methyl O-benzyl-2-desoxy-4-α-DL-threo-pentopyranoside 
• 83750-48-5 methyl O-benzoyl-3-desoxy-4-O-methyl-2-α-DL-threo-pentopyranoside 
• 83750-52-1 methyl O-benzoyl-3-O-benzyl-2-desoxy-4-α-DL-threo-pentopyranoside 
• 81686-58-0 methyl O-benzyl-2-desoxy-4-β-DL-threo-pentopyranoside 
• 83750-48-5 methyl O-benzoyl-3-desoxy-4-O-methyl-2-β-DL-threo-pentopyranoside 
• 83750-52-1 methyl O-benzoyl-3-O-benzyl-2-desoxy-4-β-DL-threo-pentopyranoside 
• 83956-18-7 (O-benzoyl-3-desoxy-4-α-DL-threo-pentopyranosyl)-1-methoxy-4-pyrimidinone-2 

Relevant academic research and scientific papers

Syntese de nucleosides pyrimidiques a partir de bromures de desoxy-4-pentopyranosyles non totalement proteges

The synthesis of nucleosides 15-19 has been completed in high yield following the method of Hilbert-Johnson, by condensation of 2,4-dimethoxypyrimidine with bromo-4-deoxypento pyranosides in which the C-3 hydroxyl group is free.The presence of this group

OUVERTURE D'EPOXYDES PAR DES ACIDES ORGANIQUES DANS L'H.M.P.T. : NOUVELLE VOIE D'ACCES A DES DESOXYPENTOPYRANOSIDES

The opening of pyranic epoxides with organic acids in HMPA leads to regioselectively esterified methyl deoxythreopentopyranosides ; one of them is a convenient intermediate to provide erythro isomers.