Use of Carbonyl Group Addition−Elimination Reactions for Synthesis of Nucleic Acid Conjugates-Reference-Cited by-同舟云学术

Use of Carbonyl Group Addition−Elimination Reactions for Synthesis of Nucleic Acid Conjugates

Published:2005-05-01 Issue:3 Volume:16 Page:471-489
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Zatsepin Timofei S.¹,Stetsenko Dmitry A.¹,Gait Michael J.¹,Oretskaya Tatiana S.¹

Affiliation:

1. Department of Chemistry, M. V. Lomonossov Moscow State University, 1 Leninskie Gory, Moscow, 119992, Russia, and Medical Research Council, Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/bc049712v

Reference168 articles.

1. Synthesis of fluorescently labelled oligonucleotides and nucleic acids

2. Ferrocene-containing nucleic acids. Synthesis and electrochemical properties

3. Site-Specific Incorporation of Nitroxide Spin-Labels into Internal Sites of the TAR RNA; Structure-Dependent Dynamics of RNA by EPR Spectroscopy

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