SYNTHETIC STUDIES TO IMPROVE THE DEUTERIUM LABELLING IN NUCLEOSIDES FOR FACILITATING STRUCTURAL STUDIES OF LARGE RNAS BY HIGH-FIELD NMR SPECTROSCOPY
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1081/NCN-100002549
Reference11 articles.
1. The Use of Non-Uniform Deuterium Labelling ['NMR-Window'] To Study the NMR Structure of a 21mer RNA Hairpin
2. The NMR structure of 31mer RNA domain of Escherichia coli RNase P RNA using its non-uniformly deuterium labelled counterpart [the 'NMR- window' concept]
3. The identification of the A-type RNA helices in a 55mer RNA by selective incorporation of deuterium-labelled nucleotide residues (Uppsala NMR-window concept)
4. Synthesis of 1′#,2′,3′,4′#,5′,5″-2H6-β-D-ribonucleosides and 1′#, 2′,2″,3′,4′#,5′,5″-2H7-β-D-2′-deoxyribonucleosides for selective suppression of proton resonances in partially-deuterated oligo-DNA, oligo-RNA and in 2,5A core (1H-NMR window)
5. Diastereospecific chemical synthesis of ribonucleosides-3′,4′,5′,5″ -d4
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3. Synthesis of[2′-2H1]-Ribonucleosides;Helvetica Chimica Acta;2004-03
4. Studies on the Stereoselective Synthesis of Deuterated D-Ribose Derivatives;Helvetica Chimica Acta;2003-03
5. Total Synthesis of 2‘,3‘,4‘,5‘,5‘ ‘-2H5-Ribonucleosides: The Key Building Blocks for NMR Structure Elucidation of Large RNA;The Journal of Organic Chemistry;2001-09-08
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