Sulfoxide-metal exchange for the synthesis of the 2′-tributylstannyl derivative of 2′,3′-didehydro-2′,3′-dideoxyuridine (d4U):: A general entry to 2′-carbon-substituted analogues of d4U

被引:4
|
作者
Kumamoto, H
Onuma, S
Tsuchiya, K
Egusa, Y
Tanaka, H
Satoh, T
机构
[1] Showa Univ, Sch Pharmaceut Sci, Shinagawa Ku, Tokyo 1428555, Japan
[2] Tokyo Univ Sci, Fac Sci, Dept Chem, Shinjyuku Ku, Tokyo 1628601, Japan
来源
关键词
D O I
10.1081/NCN-120006826
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
`Methods are described for the synthesis of the 2'-tributylstannyl derivative of 2',3'-didehydro-2',3'-dideoxyuridine (d4U). Two approaches were investigated: radical-mediated desulfonylative stannylation of the 2'-benzenesulfonyl derivative of d4U and sulfoxide-metal exchange reaction of the 2'-benzenesulfinyl derivative. The latter approach was found to give the desired 2'-stannyl derivative in good yield. It was also shown that manipulations of the stannyl group allowed the introduction of a variety of carbon-substituents to the 2'-position by applying the Stille reaction. The whole reaction sequence has opened up a highly general entry to 2'-carbon-substituted analogues of d4U.
引用
收藏
页码:275 / 286
页数:12
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