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

DOI: 10.1248/cpb.31.2164

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2164 - 2167 (1983)

Update date:2022-08-02

Topics:

Authors:

Tanaka Tanaka

Matsuda Matsuda

Iijima Iijima

Hayakawa

Miyasaka

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Article abstract of DOI:10.1248/cpb.31.2164

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

Full text of DOI:10.1248/cpb.31.2164

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Product name:2',3'-O-isopropylidene-5'-O-methoxy-methyl-6-phenylthiouridine

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