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Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives
[Image: see text] Herein we describe the construction of hexadecameric self-assembled dendrimers (SADs) using a series of dendronized 8-(m-acetylphenyl)-2′-deoxyguanosine (mAG) subunits. The azido-substituted mAG subunits were covalently linked to alkynyl polyester dendrons using a copper-catalyzed...
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Formato: | Texto |
Lenguaje: | English |
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American Chemical Society
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654094/ https://www.ncbi.nlm.nih.gov/pubmed/18452304 http://dx.doi.org/10.1021/ol800701j |
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author | Betancourt, José E. Rivera, José M. |
author_facet | Betancourt, José E. Rivera, José M. |
author_sort | Betancourt, José E. |
collection | PubMed |
description | [Image: see text] Herein we describe the construction of hexadecameric self-assembled dendrimers (SADs) using a series of dendronized 8-(m-acetylphenyl)-2′-deoxyguanosine (mAG) subunits. The azido-substituted mAG subunits were covalently linked to alkynyl polyester dendrons using a copper-catalyzed 1,3-dipolar cycloaddition reaction. Discrete SADs are formed with high fidelity and thermal stability even with the increased steric hindrance offered by the dendrons. |
format | Text |
id | pubmed-2654094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-26540942009-03-20 Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives Betancourt, José E. Rivera, José M. Org Lett [Image: see text] Herein we describe the construction of hexadecameric self-assembled dendrimers (SADs) using a series of dendronized 8-(m-acetylphenyl)-2′-deoxyguanosine (mAG) subunits. The azido-substituted mAG subunits were covalently linked to alkynyl polyester dendrons using a copper-catalyzed 1,3-dipolar cycloaddition reaction. Discrete SADs are formed with high fidelity and thermal stability even with the increased steric hindrance offered by the dendrons. American Chemical Society 2008-05-02 2008-06-05 /pmc/articles/PMC2654094/ /pubmed/18452304 http://dx.doi.org/10.1021/ol800701j Text en Copyright © 2008 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. 40.75 |
spellingShingle | Betancourt, José E. Rivera, José M. Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives |
title | Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives |
title_full | Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives |
title_fullStr | Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives |
title_full_unstemmed | Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives |
title_short | Hexadecameric Self-Assembled Dendrimers Built from 2′-Deoxyguanosine Derivatives |
title_sort | hexadecameric self-assembled dendrimers built from 2′-deoxyguanosine derivatives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654094/ https://www.ncbi.nlm.nih.gov/pubmed/18452304 http://dx.doi.org/10.1021/ol800701j |
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