A Versatile Photocleavable Bifunctional Linker for Facile Synthesis of Substrate−DNA Conjugates for the Selection of Nucleic Acid Catalysts

2007 ◽  
Vol 18 (1) ◽  
pp. 275-279 ◽  
Author(s):  
Dayal Saran ◽  
Donald H. Burke
ChemInform ◽  
2010 ◽  
Vol 27 (23) ◽  
pp. no-no
Author(s):  
J. R. LORSCH ◽  
J. W. SZOSTAK

1996 ◽  
Vol 29 (2) ◽  
pp. 103-110 ◽  
Author(s):  
Jon R. Lorsch ◽  
Jack W. Szostak

2018 ◽  
Vol 54 (50) ◽  
pp. 6927-6930 ◽  
Author(s):  
Kazuma Yokoo ◽  
Keiji Mori

We report a divergent synthesis of CF3-substituted fused skeletons based on precise control of the activation site through the selection of acid catalysts.


2020 ◽  
Vol 18 (46) ◽  
pp. 9461-9472
Author(s):  
Shinji Kumagai ◽  
Hiroaki Sawamoto ◽  
Tomo Takegawa-Araki ◽  
Yuuki Arai ◽  
Shuhei Yamakoshi ◽  
...  

Facile synthesis of GuNA (guanidine-bridged nucleic acid) phosphoramidites bearing thymine, adenine, guanine, and 5-methylcytosine nucleobases and a robust method for the preparation of GuNA-modified oligonucleotides are described.


2003 ◽  
Vol 33 (12) ◽  
pp. 1309-1317 ◽  
Author(s):  
H.Ulrich Göringer ◽  
Matthias Homann ◽  
Mihaela Lorger

2015 ◽  
Vol 6 (7) ◽  
pp. 3692-3696 ◽  
Author(s):  
G. Adornetto ◽  
A. Porchetta ◽  
G. Palleschi ◽  
K. W. Plaxco ◽  
F. Ricci

Here we explore a general strategy for the rational design of nucleic acid catalysts that can be allosterically activated by specific nucleic-acid binding proteins.


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