Modeling Duplex DNA Oligonucleotides with Modified Pyrimidine Bases

Author(s):  
John Miller ◽  
Michael Cooney ◽  
Karol Miaskiewicz ◽  
Roman Osman
2004 ◽  
Vol 126 (9) ◽  
pp. 2877-2884 ◽  
Author(s):  
Chu-Sheng Liu ◽  
Rigoberto Hernandez ◽  
Gary B. Schuster

Lab on a Chip ◽  
2012 ◽  
Vol 12 (24) ◽  
pp. 5160 ◽  
Author(s):  
Namhyun Choi ◽  
Kangsun Lee ◽  
Dong Woo Lim ◽  
Eun Kyu Lee ◽  
Soo-Ik Chang ◽  
...  

2004 ◽  
Vol 80 (3) ◽  
pp. 456 ◽  
Author(s):  
Lezah W. Roberts ◽  
Gary B. Schuster
Keyword(s):  

2020 ◽  
Author(s):  
Bapurao Bhoge ◽  
Ishu Saraogi

Chemo- and site-specific modifications in oligonucleotides have wide applicability as mechanistic probes in chemical biology. Here we have employed a classical reaction in organic chemistry, reductive amination, to selectively functionalize the N<sup>2</sup>-amine of guanine/2’-deoxyguanine monophosphate. This method specifically modifies guanine in several tested DNA oligonucleotides, while leaving the other bases unaffected. Using this approach, we have successfully incorporated desired handles chemoselectively into DNA oligomers.


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