320600-40-6

Upstream product

• 233253-71-9 (1S,3S)-3-Benzoyloxymethyl-1,3-dihydro-1-methoxybenzo[c]furan 
• 73416-11-2 bis-trimethylsilyluracil 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 139086-86-5 2-(1,3-dioxan-2-yl)benzaldehyde 
• 98-88-4 benzoyl chloride 
• 320600-36-0 (S)-1-O-Benzoyl-2-[2-(1,3-dioxan-2-yl)phenyl]ethane-1,2-diol 
• 528584-56-7 Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester 
• 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 

Relevant academic research and scientific papers

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