Synthesis of monomers bearing at the 2′-position cyanomethoxycarbonyl group for phosphoramidite oligonucleotide synthesis

Nucleosides, Nucleotides and Nucleic Acids

Volumn 23, Issue 6-7, 2004, Pages 993-998

  Vasilyeva, Svetlana V ^a   Abramova, Tatyana V ^a   Silnikov, Vladimir N ^a  

^a INSTITUTE OF CHEMICAL BIOLOGY AND FUNDAMENTAL MEDICINE   (Russian Federation)

Author keywords

Cyanomethyl esters, 2 amino uridine, 2 amino arabinoadenosine, Cyanomethoxycarbonyl; Modified nucleosides; Reactive linker groups

Indexed keywords

2' AMINOARABINOADENOSINE; 2' AMINOURIDINE; CARBONIC ACID DERIVATIVE; CARBONYL DERIVATIVE; CYANOMETHYLCARBONYL DERIVATIVE; MONOMER; NUCLEOSIDE; OLIGONUCLEOTIDE; PHOSPHORAMIDIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ACIDIFICATION; CHEMICAL REACTION; CONFERENCE PAPER; NUCLEOTIDE METABOLISM; PROTEIN STRUCTURE; STRUCTURE ANALYSIS; SYNTHESIS;

AMIDES; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; OLIGONUCLEOTIDES; PHOSPHORIC ACIDS; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 7644237492     PISSN: 15257770     EISSN: None     Source Type: Journal    
DOI: 10.1081/NCN-200026053     Document Type: Conference Paper

References (6)

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2. Polushin, N.N. The precursor strategy: terminus methoxyoxalamido modifiers for single and multiple functionalization of oligodeoxyribonucleotides. Nucleic Acids Res. 2000, 28, 3125-3133.
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