1, 1, 3, 3-Tetraisopropyl-3-(2-(triphenylmethoxy)ethoxy)disiloxane-1-yl group, a potential 5′-O-protecting group for solid-phase RNA synthesis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Preparation of ribonucleoside 3′-O-phosphoramidites and their application to the automated solid phase synthesis of oligonucleotides
2. The automated chemical synthesis of long oligoribuncleotides using 2'-O-silylated ribonucleoside 3'-O-phosphoramidites on a controlled-pore glass support: synthesis of a 43-nucleotide sequence similar to the 3'-half molecule of an Escherichia coli formylmethionine tRNA
3. An Efficient Method for the Isolation and Purification of Oligoribonucleotides
4. Chemical synthesis of RNA using fast oligonucleotide deprotection chemistry
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1. Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols;Greene's Protective Groups in Organic Synthesis;2014-08-11
2. Ruthenium-Catalyzed N-Alkylation of Amines and Sulfonamides Using Borrowing Hydrogen Methodology;Journal of the American Chemical Society;2009-01-21
3. Protecting groups for RNA synthesis: an increasing need for selective preparative methods;Chemical Society Reviews;2008
4. Alkylboron and -silicon Compounds;Comprehensive Organic Functional Group Transformations II;2005
5. Synthesis and Properties of O-β-D-Ribofuranosyl-(1″-2′)-Adenosine-5″-O-Phosphate and Its Derivatives;Nucleosides, Nucleotides and Nucleic Acids;2000-10
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