CHEMICAL SYNTHESIS OF RNA-FRAGMENT ANALOGS THAT HAVE PHOSPHOROTHIOATE LINKAGES OF IDENTICAL CONFIGURATION
被引:3
作者:
ALMER, H
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h-index: 0
机构:
UNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDENUNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN
ALMER, H
[1
]
STAWINSKI, J
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h-index: 0
机构:
UNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDENUNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN
STAWINSKI, J
[1
]
STROMBERG, R
论文数: 0引用数: 0
h-index: 0
机构:
UNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDENUNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN
STROMBERG, R
[1
]
机构:
[1] UNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN
来源:
NUCLEOSIDES & NUCLEOTIDES
|
1995年
/
14卷
/
3-5期
关键词:
D O I:
10.1080/15257779508012494
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:
Oligouridine all-Rp-phosphorothioates were synthesized using the H-phosphonate approach followed by silfurisation with S-8 and treatment with nuclease P1. The degree of stereoselection in the couplings is reported for different 2'-O-silyl protecting groups. The influence of the heterocyclic base was also investigated.