Synthesis of Oligoribonucleotides Containing N 6 ‐Alkyladenosine and 2‐Methylthio‐ N 6 ‐Alkyladenosine
Author:
Affiliation:
1. Institute of Bioorganic Chemistry, Polish Academy of Sciences Poznan Poland
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc0423s17
Reference19 articles.
1. The chemical synthesis of the anticodon loop of an eukaryotic initiator tRNA containing the hypermodified nucleoside N6-/N-threonylcarbonyl/-adenosine/t6A/1
2. Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
3. Synthesis of the Anticodon HairpintRNAfMet ContainingN-{[9-(β-D-Ribofuranosyl)-9H-purin-6-yl]carbamoyl}-L-threonine (=N6-{{[(1S,2R)-1-Carboxy-2-hydroxypropyl]amino}carbonyl}adenosine, t6A)
4. Thionation reactions of lawesson's reagents
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1. Unlocked nucleic acids: implications of increased conformational flexibility for RNA/DNA triplex formation;Biochemical Journal;2014-11-14
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