Synthesis of Oligoribonucleotides Containing 4‐Thiouridine Using the Convertible Nucleoside Approach and the 1‐(2‐Fluorophenyl)‐4‐Methoxypiperidin‐4‐yl Group-Reference-Cited by-同舟云学术

Synthesis of Oligoribonucleotides Containing 4‐Thiouridine Using the Convertible Nucleoside Approach and the 1‐(2‐Fluorophenyl)‐4‐Methoxypiperidin‐4‐yl Group

Published:2004-01-01 Issue:11 Volume:23 Page:1767-1777
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Aviñó Anna¹,García Ramon Güimil¹²,Eritja Ramon¹

Affiliation:

1. a Instituto de Biología Molecular de Barcelona , C.S.I.C. Jordi Girona 18‐26, E‐08034, Barcelona, Spain

2. b Febit ag, Käfertaler Strasse 190, Mannheim, D‐68167, Germany

Publisher

Informa UK Limited

Subject

Genetics,Molecular Medicine,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1081/NCN-200034044

Reference20 articles.

1. Photochemical cross-linking analysis of protein-nucleic acid interactions in Escherichia coli transcription complexes from lambda PR′ promoter

2. Site-specific RNA crosslinking with 4-thiouridine

3. Recombinant photoreactive tRNA molecules as probes for cross-linking studies

4. A convenient synthesis of S-cyanoethyl-protected 4-thiouridine and its incorporation into oligoribonucleotides

5. Synthesis of Uridine Phosphoramidite Analogs: Reagents for Site-Specific Incorporation of Photoreactive Sites into RNA Sequences

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