528584-56-7

Upstream product

• 139086-86-5 2-(1,3-dioxan-2-yl)benzaldehyde 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 233253-69-5 (S)-1-[2-(1,3-Dioxan-2-yl)phenyl]ethane-1,2-diol 
• 233253-68-4 [2-(1,3-dioxan-2-yl)phenyl]ethene 
• 98-88-4 benzoyl chloride 
• 474778-70-6 3,5-O-(S)-(2-ethenylbenzylidene)-1,2-O-isopropylidene-α-D-xylofuranose 
• 337903-22-7 3,5-O-(2-formylbenzylidene)-1,2-O-isopropylidene-α-D-xylofuranose 
• 549513-42-0 3,5-O-(S)[2-((S)-2-benzoyloxy-1-hydroxyethyl)benzylidene]-1,2-O-isopropylidene-α-D-xylofuranose 
• 446242-23-5 3,5-O-(S)[2-((S)-1,2-dihydroxyethyl)benzylidene]-1,2-O-isopropylidene-α-D-xylofuranose 
• 320600-36-0 (S)-1-O-Benzoyl-2-[2-(1,3-dioxan-2-yl)phenyl]ethane-1,2-diol 

Downstream Products

• 233253-71-9 (1S,3S)-3-Benzoyloxymethyl-1,3-dihydro-1-methoxybenzo[c]furan 
• 320600-38-2 (1'R,3'S)-1-(3'-benzoyloxymethyl-1',3'-dihydrobenzo[c]furan-1-yl)uracil 
• 320600-40-6 (1'S,3'S)-1-(3'-benzoyloxymethyl-1',3'-dihydrobenzo[c]furan-1-yl)uracil 

Relevant academic research and scientific papers

Asymmetric synthesis of (3S) 3-benzoyloxymethylisobenzofuranone and its 3R enantiomer as analogues of α,β-butenolides

Both enantiomers of 3-benzoyloxymethylisobenzofuranone have been obtained in good yield in six steps from phthalaldehyde using a D-xylose derivative as a chiral protecting group. The two chiral heterocycles are γ-hydroxymethyl-α,β-butenolide analogues hav

Stereoisomeric pyrimidine nucleoside analogues based on the 1,3-dihydrobenzo[c]furan core

Stereoisomeric pyrimidine nucleoside analogues based on the 1,3-dihydrobenzo[c]furan core was described. The overall yield of 3-benzoyloxymethyl-1,3-dihydro-1-methoxybenzo[c]furan from aldehyde was 42%. After removal of the protecting group the four stere

Simple and stereoselective syntheses of nucleoside analogues with a benzo[c]furan glycone moiety

A series of d4T analogues have been synthesised in which the 2',3'- didehydro-2',3'-dideoxyribose moiety is replaced by a benzo[c]furan core. A simple strategy has been developed to access a range of compounds for biological screening. In addition, a ster