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Synthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes
[Image: see text] A phthaloyl-protected aminooxymethyl-C-2′-deoxyriboside building block has been prepared and incorporated in the middle of an oligodeoxyribonucleotide. Removal of the phthaloyl protection followed by on-support oximation with either mercurated or palladated benzaldehydes yielded ol...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854833/ https://www.ncbi.nlm.nih.gov/pubmed/31737842 http://dx.doi.org/10.1021/acsomega.9b02804 |
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author | Maity, Sajal Kumar Lönnberg, Tuomas A. |
author_facet | Maity, Sajal Kumar Lönnberg, Tuomas A. |
author_sort | Maity, Sajal Kumar |
collection | PubMed |
description | [Image: see text] A phthaloyl-protected aminooxymethyl-C-2′-deoxyriboside building block has been prepared and incorporated in the middle of an oligodeoxyribonucleotide. Removal of the phthaloyl protection followed by on-support oximation with either mercurated or palladated benzaldehydes yielded oligonucleotides bearing the respective benzaldoxime metallacycles. |
format | Online Article Text |
id | pubmed-6854833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-68548332019-11-15 Synthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes Maity, Sajal Kumar Lönnberg, Tuomas A. ACS Omega [Image: see text] A phthaloyl-protected aminooxymethyl-C-2′-deoxyriboside building block has been prepared and incorporated in the middle of an oligodeoxyribonucleotide. Removal of the phthaloyl protection followed by on-support oximation with either mercurated or palladated benzaldehydes yielded oligonucleotides bearing the respective benzaldoxime metallacycles. American Chemical Society 2019-11-01 /pmc/articles/PMC6854833/ /pubmed/31737842 http://dx.doi.org/10.1021/acsomega.9b02804 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Maity, Sajal Kumar Lönnberg, Tuomas A. Synthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes |
title | Synthesis of Organometallic Oligonucleotides through
Oximation with Metalated Benzaldehydes |
title_full | Synthesis of Organometallic Oligonucleotides through
Oximation with Metalated Benzaldehydes |
title_fullStr | Synthesis of Organometallic Oligonucleotides through
Oximation with Metalated Benzaldehydes |
title_full_unstemmed | Synthesis of Organometallic Oligonucleotides through
Oximation with Metalated Benzaldehydes |
title_short | Synthesis of Organometallic Oligonucleotides through
Oximation with Metalated Benzaldehydes |
title_sort | synthesis of organometallic oligonucleotides through
oximation with metalated benzaldehydes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854833/ https://www.ncbi.nlm.nih.gov/pubmed/31737842 http://dx.doi.org/10.1021/acsomega.9b02804 |
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