Use of p-nitrophenyl chloroformate in blocking hydroxyl groups in nucleosides

Robert L. Letsinger, and Kelvin K. Ogilvie

J. Org. Chem., 1967, 32 (2), pp 296–300

DOI: 10.1021/jo01288a011

Publication Date: February 1967

Cite this:J. Org. Chem. 32, 2, 296-300

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Article

Use of p-nitrophenyl chloroformate in blocking hydroxyl groups in nucleosides

cis-Tetrahydrofuran-3,4-diol Structure as a Key Skeleton of New Protecting Groups Removable by Self-Cyclization under Oxidative Conditions

Solid-Phase Oligodeoxynucleotide Synthesis: A Two-Step Cycle Using Peroxy Anion Deprotection

Chemical Synthesis and Properties of Conformationally Fixed Diuridine Monophosphates as Building Blocks of the RNA Turn Motif

Chemical synthesis of oligonucleotides

Reactions of Nucleosides on Polymer Supports. Synthesis of Thymidylylthymidylylthymidine^*

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Article

Use of p-nitrophenyl chloroformate in blocking hydroxyl groups in nucleosides

cis-Tetrahydrofuran-3,4-diol Structure as a Key Skeleton of New Protecting Groups Removable by Self-Cyclization under Oxidative Conditions

Solid-Phase Oligodeoxynucleotide Synthesis: A Two-Step Cycle Using Peroxy Anion Deprotection

Chemical Synthesis and Properties of Conformationally Fixed Diuridine Monophosphates as Building Blocks of the RNA Turn Motif

Chemical synthesis of oligonucleotides

Reactions of Nucleosides on Polymer Supports. Synthesis of Thymidylylthymidylylthymidine*

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Reactions of Nucleosides on Polymer Supports. Synthesis of Thymidylylthymidylylthymidine^*