On the Application of t-Butyldimethylsilyl Group in Chemical RNA Synthesis. Part I.31P NMR Study of 2′-O-t-BDMSi Group Migration During Nucleoside 3′-OH Phosphorylation and Phosphitylation Reactions-Reference-Cited by-同舟云学术

On the Application of t-Butyldimethylsilyl Group in Chemical RNA Synthesis. Part I.31P NMR Study of 2′-O-t-BDMSi Group Migration During Nucleoside 3′-OH Phosphorylation and Phosphitylation Reactions

Published:1989-01 Issue:4 Volume:8 Page:463-474
ISSN:0732-8311
Container-title:Nucleosides and Nucleotides
language:en
Short-container-title:Nucleosides and Nucleotides

Author:

Milecki Jan,Dembek Piotr,Antkowiak Wieslaw Z.,Gdaniec Zofia,Mielewczyk Slawomir,Adamiak Ryszard W.

Publisher

Informa UK Limited

Subject

Genetics,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/07328318908054189

Reference40 articles.

1. The chemical synthesis of oligo- and poly-nucleotides by the phosphotriester approach

2. The Problem of 2′-Protection in Rapid Oligoribonucleotide Synthesis

3. Solid phase synthesis of the 3′-terminal nonadecaribonucleoside octadecaphosphate sequence of yeast alanine transfer ribonucleic acid

4. Chemical Synthesis of a Pentaribonucleoside Tetraphosphate Constituting the 3'-Acceptor Stem Sequence of E. coli tRNAIle Using 2'-O-(3-Methoxy-1,5-dicarbomethoxypentan-3-yl)-ribonucleoside Building Blocks. Application of a New Achiral and Acid-labile 2'-Hydroxyl Protecting Group in tRNA Synthesis.

5. The use of silyl groups in protecting the hydroxyl functions of ribonucleosides

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