Synthesis of fully protected trinucleotide building blocks on a disulphide-linked soluble support
Author:
Affiliation:
1. University Greifswald
2. Institute for Biochemistry
3. 17487 Greifswald
4. Germany
5. University of Turku
6. Department of Chemistry
7. 20014 Turku
8. Finland
Abstract
Fully protected trinucleotides are synthesized on a tetrapodal soluble support using a disulphide linkage that upon reductive cleavage allows release of the trinucleotide with free 3′-OH group for further conversion to a phosphoramidite.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/RA/D0RA10941J
Reference32 articles.
1. Trinucleotide phosphoramidites: ideal reagents for the synthesis of mixed oligonucleotides for random mutagenesis
2. Developments in Directed Evolution for Improving Enzyme Functions
3. Random Mutagenesis Methods for In Vitro Directed Enzyme Evolution
4. Preparation of trinucleotide phosphoramidites as synthons for the synthesis of gene libraries
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1. Tuning the Solubility of Soluble Support Constructs in Liquid Phase Oligonucleotide Synthesis;The Journal of Organic Chemistry;2024-09-09
2. 5'‐O‐(2‐Isopropoxyprop‐2‐yl)‐protected Phosphoramidite Building Blocks in the Liquid Phase Oligonucleotide Synthesis;European Journal of Organic Chemistry;2023-08-11
3. Stereo-Controlled Liquid Phase Synthesis of Phosphorothioate Oligonucleotides on a Soluble Support;The Journal of Organic Chemistry;2023-07-10
4. A P(V) platform for oligonucleotide synthesis;Science;2021-09-10
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