Journal of the American Chemical Society · 2006 · 35 citations · 8 references
PharmacyMolecular BiologyBioorthogonal ChemistryNucleic Acid ChemistrySynthetic BiologyDna ChemistryDna StructureNucleic Acid EngineeringNucleic Acid SynthesisOligonucleotide ChemistryChemical Modification Of OligonucleotidesOligonucleotide SynthesisPhosphoramidate OligonucleotidesPhosphoramidite ChemistryPhosphorothioate ChemistrySilyl Ether ProtectionSolid-phase Dna SynthesisSolid-phase Oligonucleotide Synthesis
A novel solid-phase phosphoramidite-based method has been developed for the synthesis of borane phosphonate DNA. Keys to this new approach are replacement of the common 5'-dimethoxytrityl blocking group with a 5'-silyl ether and the use of new protecting groups on the bases (adenine, N6-dimethoxytrityl; cytosine, N4-trimethoxytrityl; guanine, N2-[9-fluorenylmethoxycarbonyl]; thymine, N3-anisoyl). Because of these developments, it is now possible for the first time to synthesize oligodeoxynucleotides having any combination of the four 2'-deoxynucleosides and both phosphate and borane phosphonate internucleotide linkages (including oligomers having exclusively borane phosphonate linkages).
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