Synthesis of novel tetrazole C5-linked C0- and C2-ribonucleoside phosphoramidites using MePOM and POM groups for probing RNA catalysis
Research output: Contribution to journal › Article
- Shinya Harusawa
- Hiroki Yoneyama
- Daiki Fujisue
- Masayoshi Nishiura
- Mihoyo Fujitake
- Yoshihide Usami
- Zheng-yun Zhao
- Scott A. Mcphee
- Timothy J. Wilson
- David M.J. Lilley
| Original language | English |
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| Number of pages | 4 |
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| Pages | 5891-5894 |
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| Journal | Tetrahedron Letters |
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| Journal publication date | 2012 |
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| Journal number | 44 |
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| Volume | 53 |
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| DOIs | |
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| State | Published |
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Novel C5-linked C0- and C2-tetrazole ribonucleoside phosphoramidites were designed and synthesized via tetrazole C-nucleosides. Pivaloyloxymethyl (POM) and methyl-substituted POM (MePOM) groups were introduced as N-protecting groups in the tetrazole ring that can be readily removed under mild basic conditions. The phosphoramidites were successfully incorporated into the VS ribozyme substrate and hence providing a chemogenetic approach to determine which nucleobases of ribozymes function as the acid or base, in the studies of ribozyme general acid and base catalysis. © 2012 Elsevier Ltd. All rights reserved.