Nucleotide chemistry. XIII. Synthesis of oligothymidylates via phosphotriester intermediates

Robert L. Letsinger, and Kelvin K. Ogilvie

J. Am. Chem. Soc., 1969, 91 (12), pp 3350–3355

DOI: 10.1021/ja01040a042

Publication Date: June 1969

Cite this:J. Am. Chem. Soc. 91, 12, 3350-3355

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Article

Nucleotide chemistry. XIII. Synthesis of oligothymidylates via phosphotriester intermediates

Cleavable β-Cyanoethyl Isocyanide in the Ugi Tetrazole Reaction

Synthetic Method for Oligonucleotide Block by Using Alkyl-Chain-Soluble Support

Coding Macromolecules: Inputting Information in Polymers Using Monomer-Based Alphabets

An Introduction to Sequence-Controlled Polymers

Matrix Isolation Infrared and DFT Study of the Trimethyl Phosphite–Hydrogen Chloride Interaction: Hydrogen Bonding versus Nucleophilic Substitution

Matrix Assisted Synthetic Transformations: A Mosaic of Diverse Contributions. II. The Pattern Is Completed

Nuclear magnetic resonance studies of cis-syn, trans-syn, and 6-4 photodimers of thymidylyl(3'-5')thymidine monophosphate and cis-syn photodimers of thymidylyl(3'-5')thymidine cyanoethyl phosphotriester

Nonionic nucleic acid analogs. Synthesis and characterization of dideoxyribonucleoside methylphosphonates

Synthesis of ribooligonucleotides having sequences of transfer ribonucleic acids

Nucleotide synthesis. III. Nucleotide synthesis. Derivatives of thymidine containing m- and p-haloacetamidophenyl phosphate groups

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