Reaction of S-geranyl-2-thiouracil modified oligonucleotides with alkyl amines leads to the N2-alkyl isocytosine derivatives
Author:
Affiliation:
1. Institute of Organic Chemistry
2. Lodz University of Technology
3. 90-924 Lodz
4. Poland
5. Department of Bioorganic Chemistry
6. Centre of Molecular and Macromolecular Studies
7. Polish Academy of Sciences
8. 90-363 Lodz
Abstract
The yield of the synthesis ofS-geranylated oligomers depends on the alkaline conditions of oligomer deprotection; a routinely used alkyl amine protocol deliversN2-alkylisocytosine-modified side products.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01012E
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5. S-Geranyl-2-thiouridine wobble nucleosides of bacterial tRNAs; chemical and enzymatic synthesis ofS-geranylated-RNAs and their physicochemical characterization
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