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Convenient synthesis of 5′-methyl-2′-desoxyuridines
Authors:S. N. Mikhailov  N. Sh. Padyukova  K. I. Panov
Affiliation:(1) Institute of Molecular Biology, Academy of Sciences of the USSR, 117984 Moscow
Abstract:A convenient method has been developed for the synthesis of 5prime-methyl-2prime-desoxyuridines. Chlorination of 5prime-O-benzoyl-5prime-methyluridines with a mixture of Ph3P and CCl4 in DMF affords the 2prime-desoxy-2prime-chloro-derivatives, which are then reduced with tributyltin hydride. The crystalline 5prime-O-benzoyl-5prime-methyl-2prime-desoxyuridines were obtained in overall yields of 40–60%. In a similar way, 5prime-O-benzoyluridine has given 5prime-O-benzoyl-2prime-desoxyuridine.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 246–248, February, 1989.
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