Biomimetic protecting-group-free 2′, 3′-selective aminoacylation of nucleosides and nucleotides
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2011/OB/C0OB00795A
Reference32 articles.
1. The use of 5′-pbospho-2 deoxyribocytidylylriboadenosine as a facile route to chemical aminoacylation of tRNA
2. A general and efficient route for chemical aminoacylation of transfer RNAs
3. Preparation of '2,('3)-O-Acyl-pCpA derivatives as substrates for T4 RNA ligase-mediated “chemical aminoacylation”
4. Mechanism of aminoacylation of tRNA. Proof of the aminoacyl adenylate pathway for the isoleucyl- and tyrosyl-tRNA synthetases from Escherichia coli K12
5. Mechanism of aminoacylation of transfer RNA. A pre-steady-state analysis of the reaction pathway catalyzed by the methionyl-tRNA synthetase of Bacillus stearothermophilus
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