Universal 2‐(4‐Nitrophenyl)ethyl and 2‐(4‐Nitrophenyl)ethoxycarbonyl Protecting Groups for Nucleosides and Nucleotides-Reference-Cited by-同舟云学术

Universal 2‐(4‐Nitrophenyl)ethyl and 2‐(4‐Nitrophenyl)ethoxycarbonyl Protecting Groups for Nucleosides and Nucleotides

Published:2007-09 Issue:1 Volume:30 Page:
ISSN:1934-9270
Container-title:Current Protocols in Nucleic Acid Chemistry
language:en
Short-container-title:Current Protocols in Nucleic Acid Chemistry

Author:

Pfleiderer Wolfgang¹

Affiliation:

1. Konstanz University Konstanz Germany

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc0213s30

Reference31 articles.

1. In situactivation of bis-dialkylaminophosphines—a new method for synthesizing deoxyoligonucleotides on polymer supports

2. Growth Inhibition of Escherichia coli by New Thymidine Analogs

3. Über methylierte Nucleoside und Purine und ihre pharmakologischen Wirkungen, I. Mitteil.: Methylierung von Nucleosiden durch Diazomethan

4. 462. Nucleotides. Part XXXVII. The structure of uridylic acids a and b, and a synthesis of spongouridine (3-β-D-arabofuranosyluracil)

5. M.H. Caruthers S.L. Beaucage C. Becker W. Efcavitch E.F. Fisher G. Galluppi P. DdeHaseth F. Martin M. Mateucci Y. Stabinsky J.K. Setlow A. Hollaender 1982 Plenum Press New York 1

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1. Nucleobase Protection of Deoxyribo‐ and Ribonucleosides;Current Protocols in Nucleic Acid Chemistry;2017-06

2. 2′-Deoxyriboguanylurea, the primary breakdown product of 5-aza-2′-deoxyribocytidine, is a mutagen, an epimutagen, an inhibitor of DNA methyltransferases and an inducer of 5-azacytidine-type fragile sites;Nucleic Acids Research;2012-07-31