Efficient Solid Phase Synthesis of Cleavable Oligodeoxynucleotides Based on a Novel Strategy for the Synthesis of 5?-S-(4,4?-Dimethoxytrityl)-2?-deoxy-5?-thionucleoside Phosphoramidites-Reference-Cited by-同舟云学术

Efficient Solid Phase Synthesis of Cleavable Oligodeoxynucleotides Based on a Novel Strategy for the Synthesis of 5?-S-(4,4?-Dimethoxytrityl)-2?-deoxy-5?-thionucleoside Phosphoramidites

Published:2004-11 Issue:11 Volume:87 Page:2812-2828
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Jahn-Hofmann Kerstin,Engels Joachim?W.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference30 articles.

1. Chemical synthesis of oligonucleotides containing a free sulphydryl group and subsequent attachment of thiol specific probes

2. The synthesis of protected 5′-mercapto-2′,5′-dideoxyribonucleoside-3′-0-phosphorainidites; uses of 5′-mercapto-oligodeoxyribonucleotides

3. Synthesis and properties of dithymidine phosphate analogues containing 3′-thiothymidine

4. Synthesis and selective cleavage of an oligodeoxynucleotide containing a bridged intemucleotide 5′-phosphorothioate linkage

5. Cleavage properties of an oligonuclotide containing a bridged internucleotide 5′-phosphorothioate RNA linkage

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