Title
Post-Synthetic Chemical Functionalization Of Oligonucleotides
Keywords
Amide; Cycloaddition; Disulfide; Hydrazone; Native chemical ligation; Oligonucleotide conjugation; Oxime; Photo-induced reaction; Thioether; Transferases
Abstract
The rapidly growing interest in synthetic oligonucleotides originates from their capability to regulate gene expressions, their high binding affinity to molecular targets, and their ability to exert enzymatic functions. However, the therapeutic and diagnostic applications of oligonucleotides are limited by their intrinsic properties. To address these challenges, chemical modifications have been applied to oligonucleotides to achieve greater potency, enhanced stability, and desired bioavailability. This chapter focuses on the major protocols developed in recent years for oligonucleotide postsynthetic modifications and provides detailed examples of each reaction category along with the relevant applications of the resulting oligonucleotide conjugates. © 2014 Elsevier Ltd. All rights reserved.
Publication Date
1-1-2014
Publication Title
Comprehensive Organic Synthesis: Second Edition
Volume
9
Number of Pages
463-493
Document Type
Article; Book Chapter
Personal Identifier
scopus
DOI Link
https://doi.org/10.1016/B978-0-08-097742-3.00908-3
Copyright Status
Unknown
Socpus ID
84903493143 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/84903493143
STARS Citation
Yuan, Yu and Wang, Weimin, "Post-Synthetic Chemical Functionalization Of Oligonucleotides" (2014). Scopus Export 2010-2014. 9064.
https://stars.library.ucf.edu/scopus2010/9064