Synthesis of Peptide Nucleic Acids Containing Pyridazine Derivatives As Cytosine and Thymine Analogs, and Their Duplexes with Complementary Oligodeoxynucleotides-Reference-Cited by-同舟云学术

Synthesis of Peptide Nucleic Acids Containing Pyridazine Derivatives As Cytosine and Thymine Analogs, and Their Duplexes with Complementary Oligodeoxynucleotides

Published:2015-03-10 Issue:6 Volume:17 Page:1609-1612
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tomori Takahito¹,Miyatake Yuya¹,Sato Yuta¹,Kanamori Takashi¹,Masaki Yoshiaki¹,Ohkubo Akihiro¹,Sekine Mitsuo¹,Seio Kohji¹

Affiliation:

1. Department of Life Science, Tokyo Institute of Technology, 4259 Nagatsuta, Midoriku, Yokohama 226-8501, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00522

Reference35 articles.

1. Modular and Practical Synthesis of 6-Substituted Pyridin-3-yl C-Nucleosides

2. Conversion of 2-deoxy-d-ribose into 2-amino-5-(2-deoxy-β-d-ribofuranosyl)pyridine, 2′-deoxypseudouridine, and other C-(2′-deoxyribonucleosides)

3. Synthesis of 5-(β-D-ribofuranosyl)-pyridin-2-one: A “deletion-modiffied” analogue of uridine

4. An unnatural base pair for incorporating amino acid analogs into proteins

5. Synthesis of 6-Substituted 2(1H)-Pyridon-3-yl C-2′-Deoxyribonucleosides

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