Synthesis 2014; 46(20): 2815-2825
DOI: 10.1055/s-0034-1378451
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of C4-Linked C0- and C2-Imidazole 2′-Deoxyribonucleoside Phos­phoramidites and Imidazole Base-Pairing Effects on DNA

Shinya Harusawa*
a   Laboratory of Pharmaceutical Organic Chemistry, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan   Fax: +81(72)6901086   eMail: harusawa@gly.oups.ac.jp
,
Hiroki Yoneyama
a   Laboratory of Pharmaceutical Organic Chemistry, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan   Fax: +81(72)6901086   eMail: harusawa@gly.oups.ac.jp
,
Yoshihide Usami
a   Laboratory of Pharmaceutical Organic Chemistry, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan   Fax: +81(72)6901086   eMail: harusawa@gly.oups.ac.jp
,
Daisuke Yamamoto
b   Biomedical Computation Center, Osaka Medical College, 2-7 Daigakucho, Takatsuki, Osaka 569-8686, Japan
,
Zheng-yun Zhao
c   Centre for Plant Science & Bio-polymer Research, Faculty of Engineering, Computing and Creative Industries, Edinburgh Napier University, 10 Colinton Road, Edinburgh, EH10 5DT, UK
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Publikationsverlauf

Received: 20. Mai 2014

Accepted after revision: 17. Juni 2014

Publikationsdatum:
31. Juli 2014 (online)


Abstract

The synthesis of C4-linked imidazole C0- and C2-2′-deoxyribonucleoside phosphoramidites (dPAs), in which the final phosphitylations are greatly improved by 4,5-dicyanoimidazole-promoted conversion, is described. The respective dPAs are successfully incorporated into the sequence of a 15-nt DNA, and the abilities of one or two imidazoles to pair with different bases are investigated through thermal melting (T m) experiments on the resulting DNA duplexes. Furthermore, computational models of the imidazole-modified DNAs are found to be in good agreement with the results of the thermal melting experiments.

Supporting Information