STUDIES ON REACTIONS OF NUCLEOSIDE H-PHOSPHONATES WITH BIFUNCTIONAL REAGENTS .3. FURTHER-STUDIES ON TRANSESTERIFICATION OF NUCLEOSIDE H-PHOSPHONATE DIESTERS WITH AMINO-ALCOHOLS
[2] UNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN
来源:
NUCLEOSIDES & NUCLEOTIDES
|
1995年
/
14卷
/
3-5期
基金:
瑞典研究理事会;
关键词:
D O I:
10.1080/15257779508012484
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:
Reactions of 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl 2-cyanoethyl phosphonate with alcohols, amines and amino alcohols in pyridine are described. Transesterification was found to be faster than beta-elimination of 2-cyanoethyl group.