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New strategies for the synthesis of unmodified and modified oligonucleotides
Author(s) -
Masayuki Sekine,
Akihiro Ohkubo,
Kohji Seio
Publication year - 2008
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/nrn020
Subject(s) - oligonucleotide , nucleobase , combinatorial chemistry , dna , cytosine , dna synthesis , base pair , chemistry , base (topology) , oligonucleotide synthesis , biochemistry , mathematics , mathematical analysis
In this paper, our recent studies on the synthesis of unmodified and modified oligonucleotides are comprehensively reviewed. We have developed a new synthetic strategy using TrS, a new 5'-protecting group, that enabled us to reduce one of the steps previously required for DNA synthesis. The "activated phosphite method" without base protection could provide a new tool for the synthesis of DNA oligomers involving base-labile functional groups such as N-acylated nucleobases capable of Watson-Crick base pairing. This new method was successfully applied to the synthesis of oligodeoxynucleotides incorporating cytosine N-oxide or adenine N-oxide that could not be synthesized by the current methods. Furthermore, several approaches we recently developed for the synthesis of several kinds of 2'-O-modified RNA oligomers will be reported.

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