85451-50-9

Upstream product

• 80614-90-0 2',3'-O-isopropylidene-5'-O-methoxy-methyl-6-phenylthiouridine 
• 80614-78-4 2',3'-O-isopropylidene-5'-O-methoxymethyl-uridine 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 85451-51-0 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(2,4-dioxo-6-phenylsulfanyl-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 87060-14-8 6-phenylthiouridine 5'-phosphate 
• 58367-11-6 6-benzylthiouridine 

Relevant academic research and scientific papers

Synthesis and biological activities of 5-substituted 6-phenylthio and 6-iodouridines, a new class of antileukemic nucleosides

A new class of 5,6-disubstituted uridines, in which the C-6 position was occupied by phenylthio group or iodine, were synthesized via lithiation of the corresponding 5-substituted 2',3'-O-isopropylidene-5'-O-methoxymethyl-uridines and subsequent electroph

"UMPOLUNG" OF REACTIVITY AT THE C-6 POSITION OF URIDINE: A SIMPLE AND GENERAL METHOD FOR 6-SUBSTITUTED URIDINES

Lithiated 2',3'-O-isopropylidene-5'-O-methoxymethyl-uridine was found to react with a variety of electrophilic reagents regiospecifically at the C-6 position.The protecting groups of the ribose moiety in the 6-functionalized products were concurrently rem