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Synthesis of a Convertible Linker Containing a Disulfide Group for Oligonucleotide Functionalization

Authors: Pontarelli ALiu JTMovasat HMénard SOh JKWilds CJ


Affiliations

1 Department of Chemistry and Biochemistry, Faculty of Arts and Science, Concordia University, 7141 Rue Sherbrooke Ouest, Montréal, Québec H4B 1R6, Canada.

Description

The synthesis and incorporation of a tosylated phosphoramidite linker containing a disulfide bond is described. Incorporation of the linker into short DNA and RNA oligomers proceeded efficiently using automated solid phase synthesis. Treatment of the support bound oligonucleotide followed by cleavage from the solid support provided a variety of common functional handles, expanding the strategies of bifunctional modification of synthetic oligonucleotides for conjugation applications.


Links

PubMed: https://pubmed.ncbi.nlm.nih.gov/35863757/

DOI: 10.1021/acs.orglett.2c02149