Specific chemical synthesis of ribonucleoside O-benzyl ethers

Leon F. Christensen, and Arthur D. Broom

J. Org. Chem., 1972, 37 (22), pp 3398–3401

DOI: 10.1021/jo00795a003

Publication Date: November 1972

Cite this:J. Org. Chem. 37, 22, 3398-3401

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Article

Specific chemical synthesis of ribonucleoside O-benzyl ethers

Structure-Guided Design of a Methyl Donor Cofactor That Controls a Viral Histone H3 Lysine 27 Methyltransferase Activity

Comparing In Vitro and In Vivo Activity of 2′-O-[2-(Methylamino)-2-oxoethyl]- and 2′-O-Methoxyethyl-Modified Antisense Oligonucleotides

Synthesis of 2‘-C-α-(Hydroxyalkyl) and 2‘-C-α-Alkylcytidine Phosphoramidites: Analogues for Probing Solvent Interactions with RNA

Facile Deprotection of O-Cbz-Protected Nucleosides by Hydrogenolysis: An Alternative to O-Benzyl Ether-Protected Nucleosides

Synthesis of 2‘-O-[2-[(N,N-Dimethylamino)oxy]ethyl] Modified Nucleosides and Oligonucleotides

Single addition substrates for the synthesis of specific oligoribonucleotides with polynucleotide phosphorylase. Synthesis of 2'-O-(α-methoxyethyl)nucleoside 5'-diphosphates

Verbesserte Einsatzm�glichkeiten des 4-Methoxybenzylrestes als 2?-OH-Schutz bei Ribonucleotidsynthesen durch TFA-Acidolyse

2-O-Benzyl-D-ribose und 2′-O-Benzyladenosin

Nucleotide, IV. Stereochemie von Diuridyl-phenylphosphaten

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