Alternatives to the 4,4′-dimethoxytrityl (DMTr) protecting group
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Studies on Polynucleotides. XXIV.1 The Stepwise Synthesis of Specific Deoxyribopolynucleotides (4).2 Protected Derivatives of Deoxyribonucleosides and New Syntheses of Deoxyribonucleoside-3″ Phosphates3
2. The 9-phenylxanthen-9-yl protecting group
3. Some substituted 9-phenylxanthen-9-yl protecting groups
4. An acetal group suitable for the protection of 2′-hydroxy functions in rapid oligoribonucleotide synthesis
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1. An Update on Protection of 5′‐Hydroxyl Functions of Nucleosides and Oligonucleotides;Current Protocols;2024-03
2. Regioselective 2,7-dimethyl-9-phenyl xanthen-9-yl protection and deprotection of nucleosides under mild conditions;Tetrahedron Letters;2023-05
3. Novel 1‐O‐Sulfono‐α‐d‐Fructofuranosyl Sulfones as Possible Inhibitors of Human GnT‐I Enzyme;ChemistrySelect;2020-04-28
4. Renewable amberlyst-15 catalyzed highly regioselective tritylation and deprotection of sugar-based diols;Journal of Carbohydrate Chemistry;2018-06-13
5. DDQ mediated regiospecific protection of primary alcohol and deprotection under neutral conditions: Application of new p -methoxy benzyl-pixyl ether as reagent of choice for nucleoside protection;Tetrahedron Letters;2017-06
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