scholarly journals The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups

1987 ◽  
Vol 15 (2) ◽  
pp. 397-416 ◽  
Author(s):  
J.C. Schulhof ◽  
D. Molko ◽  
R. Teoule
1986 ◽  
Vol 17 (32) ◽  
Author(s):  
L. J. MCBRIDE ◽  
R. KIERZEK ◽  
S. L. BEAUCAGE ◽  
M. H. CARUTHERS

2010 ◽  
Vol 12 (11) ◽  
pp. 2496-2499 ◽  
Author(s):  
Akihiro Ohkubo ◽  
Yasukazu Kuwayama ◽  
Yudai Nishino ◽  
Hirosuke Tsunoda ◽  
Kohji Seio ◽  
...  

1998 ◽  
Vol 45 (4) ◽  
pp. 949-976 ◽  
Author(s):  
K Kamaike ◽  
H Takahashi ◽  
K Morohoshi ◽  
N Kataoka ◽  
T Kakinuma ◽  
...  

A comparative study on the utility of 2-(levulinyloxymethyl)-5-nitrobenzoyl (LMNBz) and 2-(levulinyloxymethyl)benzoyl (LMBz) protecting groups for the 5'-positions of nucleoside 3'-phosphoramidite derivatives in the oligonucleotide synthesis is presented in terms of the syntheses of TpTpT, TpTpTpT, and UpCpApGpUpUpGpG. In addition we describe the synthesis, using the LMNBz protecting group, of the CpCpA terminus triplet of tRNAs bearing exocyclic amino groups with 15N-labeling, and the trimer Gp[A*]pG containing 2'-O-(beta-D-ribofuranosyl)adenosine ([A*]), the latter of which is found at position 64 in the yeast initiator tRNA(Met).


ChemInform ◽  
2010 ◽  
Vol 22 (14) ◽  
pp. no-no
Author(s):  
R. K. SINGH ◽  
A. DIKSHIT ◽  
M. CHADDHA ◽  
G. WATAL ◽  
K. MISRA

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