The 1,1- dianisyl-2,2,2-trichloroethyl group as 2′-hydroxyl protection of ribonucleotides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. 1,1-Dianisyl-2,2,2-trichloroethyl ethers — A new protection for the hydroxyl group
2. Fragmentation with supernucleophiles—VI
3. New methods in peptide synthesis, based on supernucleophiles
4. Synthesis of deoxyoligonucleotides on a polymer support
5. [15] Chemical synthesis of deoxyoligonucleotides by the phosphoramidite method
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Protective groups in the chemical synthesis of oligoribonucleotides;Russian Journal of Bioorganic Chemistry;2013-01
2. ChemInform Abstract: The 1,1-Dianisyl-2,2,2-trichloroethyl Group as 2′-Hydroxyl Protection of Ribonucleotides.;ChemInform;2010-08-05
3. Nucleotides, Part LXVIII, Acetals as New 2′-O-Protecting Functions for the Synthesis of Oligoribonucleotides: Synthesis of Monomeric Building Units and Oligoribonucleotides;Helvetica Chimica Acta;2001-05-16
4. Reactions at Oxygen Atoms;Glycoscience: Chemistry and Chemical Biology I–III;2001
5. Strategies for Oligoribonucleotide Synthesis According to the Phosphoramidite Method;Current Protocols in Nucleic Acid Chemistry;2000-02
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