An Efficient Method for the Synthesis of [4–15N]Cytidine, 2′-Deoxy[4–15N]Cytidine, [6–15N]adenosine, and 2′-Deoxy [6–15N]adenosine Derivatives-Reference-Cited by-同舟云学术

An Efficient Method for the Synthesis of [4–15N]Cytidine, 2′-Deoxy[4–15N]Cytidine, [6–15N]adenosine, and 2′-Deoxy [6–15N]adenosine Derivatives

Published:1996-01 Issue:1-3 Volume:15 Page:749-769
ISSN:0732-8311
Container-title:Nucleosides and Nucleotides
language:en
Short-container-title:Nucleosides and Nucleotides

Author:

Kamaike Kazuo¹,Takahashi Mihoko¹,Utsugi Kazuyuki¹,Tomizuka Kazue¹,Okazaki Yasunori¹,Tamada Yuri¹,Kinoshita Kazutomo¹,Masuda Hiroyuki¹,Ishido Yoshiharu¹

Affiliation:

1. a Laboratory of Pharmaceutical Chemistry, School of Pharmacy, Tokyo University of Pharmacy and Life Science , 1432-1 Horinouchi, Hachioji , Tokyo , 192-03 , Japan

Publisher

Informa UK Limited

Subject

Genetics,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/07328319608002421

Reference28 articles.

1. An efficient method for the synthesis of [4-15N]cytidine and [6-15N]adenosine derivatives from uridine and inosine

2. NMR studies of the complex between the decadeoxynucleotide d(GCATTAATGC)2 and a minor-groove-binding drug

3. Conformation of the DNA undecamer 5′d(A-A-G-T-G-T-G-A-T-A-T) bound to the single-stranded DNA binding protein of Escherichia coli

4. 1H NMR sudy of the interaction of bacteriophageλ Cro protein with the OR3 operator. Evidence for a change of the conformation of the OR3 operator on binding

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