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Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid
IsoGNA, an isomer of glycerol nucleic acid GNA, is a flexible (acyclic) nucleic acid with bases directly attached to its linear backbone. IsoGNA exhibits (limited) base-pairing properties which are unique compared to other known flexible nucleic acids. Herein, we report on the details of the prepara...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168771/ https://www.ncbi.nlm.nih.gov/pubmed/25246971 http://dx.doi.org/10.3762/bjoc.10.220 |
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author | Kim, Keunsoo Punna, Venkateshwarlu Karri, Phaneendrasai Krishnamurthy, Ramanarayanan |
author_facet | Kim, Keunsoo Punna, Venkateshwarlu Karri, Phaneendrasai Krishnamurthy, Ramanarayanan |
author_sort | Kim, Keunsoo |
collection | PubMed |
description | IsoGNA, an isomer of glycerol nucleic acid GNA, is a flexible (acyclic) nucleic acid with bases directly attached to its linear backbone. IsoGNA exhibits (limited) base-pairing properties which are unique compared to other known flexible nucleic acids. Herein, we report on the details of the preparation of isoGNA phosphoramidites and an alternative route for the synthesis of the adenine derivative. The synthetic improvements described here enable an easy access to isoGNA and allows for the further exploration of this structural unit in oligonucleotide chemistry thereby spurring investigations of its usefulness and applicability. |
format | Online Article Text |
id | pubmed-4168771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-41687712014-09-22 Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid Kim, Keunsoo Punna, Venkateshwarlu Karri, Phaneendrasai Krishnamurthy, Ramanarayanan Beilstein J Org Chem Full Research Paper IsoGNA, an isomer of glycerol nucleic acid GNA, is a flexible (acyclic) nucleic acid with bases directly attached to its linear backbone. IsoGNA exhibits (limited) base-pairing properties which are unique compared to other known flexible nucleic acids. Herein, we report on the details of the preparation of isoGNA phosphoramidites and an alternative route for the synthesis of the adenine derivative. The synthetic improvements described here enable an easy access to isoGNA and allows for the further exploration of this structural unit in oligonucleotide chemistry thereby spurring investigations of its usefulness and applicability. Beilstein-Institut 2014-09-08 /pmc/articles/PMC4168771/ /pubmed/25246971 http://dx.doi.org/10.3762/bjoc.10.220 Text en Copyright © 2014, Kim et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Kim, Keunsoo Punna, Venkateshwarlu Karri, Phaneendrasai Krishnamurthy, Ramanarayanan Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid |
title | Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid |
title_full | Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid |
title_fullStr | Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid |
title_full_unstemmed | Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid |
title_short | Synthesis of phosphoramidites of isoGNA, an isomer of glycerol nucleic acid |
title_sort | synthesis of phosphoramidites of isogna, an isomer of glycerol nucleic acid |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168771/ https://www.ncbi.nlm.nih.gov/pubmed/25246971 http://dx.doi.org/10.3762/bjoc.10.220 |
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