The isopropoxyacetic group for convenient base protection during solid-support synthesis of oligodeoxyribonucleotides and their triester analogs
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/17/12/4863/7043868/17-12-4863.pdf
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1. Modified internucleoside linkages for nuclease-resistant oligonucleotides;RSC Chemical Biology;2021
2. Nucleobase Protection of Deoxyribo‐ and Ribonucleosides;Current Protocols in Nucleic Acid Chemistry;2017-06
3. Solid-Phase Synthesis, Hybridizing Ability, Uptake, and Nuclease Resistant Profiles of Position-Selective Cationic and Hydrophobic Phosphotriester Oligonucleotides;The Journal of Organic Chemistry;2015-09-03
4. Application of activated nucleoside analogs for the treatment of drug-resistant tumors by oral delivery of nanogel-drug conjugates;Journal of Controlled Release;2013-04
5. An Efficient One-pot N-Acylation of Deoxy- and Ribo-cytidine Using Carboxylic Acids Activated in situ with 2-Chloro-4,6-dimethoxy-1,3,5-triazine;Bulletin of the Korean Chemical Society;2010-07-20
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