Post‐Synthetic Modification of Oligonucleotides Through Oxidative Amination of 4‐Thio‐2′‐Deoxyuridine-Reference-Cited by-同舟云学术

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Post‐Synthetic Modification of Oligonucleotides Through Oxidative Amination of 4‐Thio‐2′‐Deoxyuridine

Published:2021-10 Issue:10 Volume:1 Page:
ISSN:2691-1299
Container-title:Current Protocols
language:en
Short-container-title:Current Protocols

Author:

Wang Jingyi¹,Shang Jiachen¹,Xiang Yu¹,Tong Aijun¹

Affiliation:

1. Department of Chemistry, Beijing Key Laboratory for Microanalytical Methods and Instrumentation, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education) Tsinghua University Beijing China

Publisher

Wiley

Subject

Medical Laboratory Technology,Health Informatics,General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cpz1.274

Reference13 articles.

1. The Functionalization of Oligonucleotides Via Phosphoramidite Derivatives

2. Synthesis and Postsynthetic Modification of Oligodeoxynucleotides Containing 4-Thio-2'-deoxyuridine (ds4U)

3. Synthesis of a 4-thio-2'-deoxyuridine containing oligonucleotide. Development of the thiocarbonyl group as a linker element.

4. Thiation of Nucleosides. II. Synthesis of 5-Methyl-2'-deoxycytidine and Related Pyrimidine Nucleosides1

5. Permanganate oxidation of 4-thiouracil derivatives. Isolation and properties of 1-substituted-2-pyrimidone-4-sulfonates

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