Synthesis, Characterization, and Binding Property of Isoelectronic Analogues of Nucleobases, B(6)-Substituted 5-Aza-6-borauracils and -thymines-Reference-Cited by-同舟云学术

Synthesis, Characterization, and Binding Property of Isoelectronic Analogues of Nucleobases, B(6)-Substituted 5-Aza-6-borauracils and -thymines

Published:2010-06-29 Issue:15 Volume:12 Page:3386-3389
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ito Hiroshi¹,Yumura Kyohei¹,Saigo Kazuhiko¹

Affiliation:

1. Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-8656, Japan, and School of Environmental Science and Engineering, Kochi University of Technology, Miyanokuch, Tosayamada-cho, Kami-shi, Kochi 782-8502, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol1012058

Reference37 articles.

1. For a review see:

2. B-N as a C-C substitute in aromatic systems

3. 624. New heteroaromatic compounds. Part I. 9-Aza-10-boraphenanthrene

4. 625. New heteroaromatic compounds. Part II. Boron compounds isoconjugate with indole, 2 : 3-benzofuran, and thionaphthen

5. New Heteroaromatic Compounds. XIV.1 Boron-containing Analogs of Purine, Quinazoline and Perimidine

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