Triphenylmethanesulfenyl Group. A New Protecting Group for the Uracil Residue in Oligoribonucleotide Synthesis
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference20 articles.
1. Reaction between 1-arenesulphonyl-3-nitro-1,2,4-triazoles and nucleoside base residues. Elucidation of the nature of side-reactions during oligonucleotide synthesis.
2. The protection of uracil and guanine residues in oligonucleotide synthesis
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1. Nucleobase Protection of Deoxyribo‐ and Ribonucleosides;Current Protocols in Nucleic Acid Chemistry;2017-06
2. Synthesis of Branched DNA Using Oxidatively Cleavable Tritylsulfenyl as a Hydroxy Protecting Group;Current Protocols in Nucleic Acid Chemistry;2014-09
3. Protection for the Phosphate Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
4. Protection for the Amino Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
5. cis-Tetrahydrofuran-3,4-diol Structure as a Key Skeleton of New Protecting Groups Removable by Self-Cyclization under Oxidative Conditions;The Journal of Organic Chemistry;2006-08-26
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