A New Method for the Preparation of Modified Oligonucleotides
Olga Gorchs, Marta Cabrero Hernández, Lourdes Garriga, Enrique Pedroso, Anna Grandas, Jaume Farràs
Abstract
Olga Gorchs, Marta Cabrero Hernández, Lourdes Garriga, Enrique Pedroso, Anna Grandas, Jaume Farràs
Abstract
[reaction-see text] N-Nitrothymidine can be transformed into a phosphoramidite building block suitable for oligonucleotide synthesis using the standard phosphite triester solid-phase approach. The N-nitrothymidine residues remain stable during the elongation cycles and react smoothly with primary amines, furnishing oligonucleotides containing N3-modified thymidines. A number of N3-substituted oligonucleotides have been prepared using this methodology, some of them incorporating aminoalkyl or hydroxyalkyl groups.
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[reaction-see text] N-Nitrothymidine can be transformed into a phosphoramidite building block suitable for oligonucleotide synthesis using the standard phosphite triester solid-phase approach. The N-nitrothymidine residues remain stable during the elongation cycles and react smoothly with primary amines, furnishing oligonucleotides containing N3-modified thymidines. A number of N3-substituted oligonucleotides have been prepared using this methodology, some of them incorporating aminoalkyl or hydroxyalkyl groups.
Key concepts: Phosphoramidite, Oligonucleotide, Chemistry, Combinatorial chemistry, Elongation, Block (permutation group theory), Solid-phase synthesis, Biochemistry