Use of isobutyloxycarbonyl as a blocking group in preparation of 3'-O-(p-methoxytrityl)thymidine

Kelvin K. Ogilvie, and Robert L. Letsinger

J. Org. Chem., 1967, 32 (7), pp 2365–2366

DOI: 10.1021/jo01282a066

Publication Date: July 1967

Cite this:J. Org. Chem. 32, 7, 2365-2366

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Article

Use of isobutyloxycarbonyl as a blocking group in preparation of 3'-O-(p-methoxytrityl)thymidine

N-Terminal Protein Modification Using Simple Aminoacyl Transferase Substrates

Oligonucleotide N-alkylphosphoramidates: synthesis and binding to polynucleotides

Syntheses and configurational analyses of thymidine 4-nitrophenyl [17O,18O]phosphates and the stereochemical course of a reaction catalyzed by bovine pancreatic deoxyribonuclease I

Duplex formation of a nonionic oligo(deoxythymidylate) analog [heptadeoxythymidylyl-(3'-5')-deoxythymidine heptaethyl ester (d-[Tp(Et)]₇T)]with poly(deoxyadenylate). Evaluation of the electrostatic interaction

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Article

Use of isobutyloxycarbonyl as a blocking group in preparation of 3'-O-(p-methoxytrityl)thymidine

N-Terminal Protein Modification Using Simple Aminoacyl Transferase Substrates

Oligonucleotide N-alkylphosphoramidates: synthesis and binding to polynucleotides

Syntheses and configurational analyses of thymidine 4-nitrophenyl [17O,18O]phosphates and the stereochemical course of a reaction catalyzed by bovine pancreatic deoxyribonuclease I

Duplex formation of a nonionic oligo(deoxythymidylate) analog [heptadeoxythymidylyl-(3'-5')-deoxythymidine heptaethyl ester (d-[Tp(Et)]7T)]with poly(deoxyadenylate). Evaluation of the electrostatic interaction

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Duplex formation of a nonionic oligo(deoxythymidylate) analog [heptadeoxythymidylyl-(3'-5')-deoxythymidine heptaethyl ester (d-[Tp(Et)]₇T)]with poly(deoxyadenylate). Evaluation of the electrostatic interaction