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Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
Maleimide-containing fluorinated porphyrins and chlorins were prepared based on the reaction of Zn(II) or Ni(II) complexes of 5,10,15,20-tetrakis(4-amino-2,3,5,6-tetrafluorophenyl)porphyrin and chlorin with maleic anhydride. Porphyrin maleimide derivatives were also prepared by the reaction of 5,10,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880841/ https://www.ncbi.nlm.nih.gov/pubmed/31807205 http://dx.doi.org/10.3762/bjoc.15.263 |
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author | Ol’shevskaya, Valentina A Kononova, Elena G Zaitsev, Andrei V |
author_facet | Ol’shevskaya, Valentina A Kononova, Elena G Zaitsev, Andrei V |
author_sort | Ol’shevskaya, Valentina A |
collection | PubMed |
description | Maleimide-containing fluorinated porphyrins and chlorins were prepared based on the reaction of Zn(II) or Ni(II) complexes of 5,10,15,20-tetrakis(4-amino-2,3,5,6-tetrafluorophenyl)porphyrin and chlorin with maleic anhydride. Porphyrin maleimide derivatives were also prepared by the reaction of 5,10,15,20-tetrakis(4-azido-2,3,5,6-tetrafluorophenyl)porphyrinato Zn(II) or Ni(II) with N-propargylmaleimide via the CuAAC click reaction to afford fluorinated porphyrin–triazole–maleimide conjugates. New maleimide derivatives were isolated in reasonable yields and identified by UV–vis, (1)H NMR, (19)F NMR spectroscopy and mass-spectrometry. |
format | Online Article Text |
id | pubmed-6880841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-68808412019-12-05 Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization Ol’shevskaya, Valentina A Kononova, Elena G Zaitsev, Andrei V Beilstein J Org Chem Letter Maleimide-containing fluorinated porphyrins and chlorins were prepared based on the reaction of Zn(II) or Ni(II) complexes of 5,10,15,20-tetrakis(4-amino-2,3,5,6-tetrafluorophenyl)porphyrin and chlorin with maleic anhydride. Porphyrin maleimide derivatives were also prepared by the reaction of 5,10,15,20-tetrakis(4-azido-2,3,5,6-tetrafluorophenyl)porphyrinato Zn(II) or Ni(II) with N-propargylmaleimide via the CuAAC click reaction to afford fluorinated porphyrin–triazole–maleimide conjugates. New maleimide derivatives were isolated in reasonable yields and identified by UV–vis, (1)H NMR, (19)F NMR spectroscopy and mass-spectrometry. Beilstein-Institut 2019-11-13 /pmc/articles/PMC6880841/ /pubmed/31807205 http://dx.doi.org/10.3762/bjoc.15.263 Text en Copyright © 2019, Ol’shevskaya et al. https://creativecommons.org/licenses/by/4.0https://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/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Letter Ol’shevskaya, Valentina A Kononova, Elena G Zaitsev, Andrei V Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization |
title | Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization |
title_full | Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization |
title_fullStr | Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization |
title_full_unstemmed | Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization |
title_short | Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization |
title_sort | fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880841/ https://www.ncbi.nlm.nih.gov/pubmed/31807205 http://dx.doi.org/10.3762/bjoc.15.263 |
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