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Higher Analogues of Resorcinarenes and Pyrogallolarenes: Bricks for Supramolecular Chemistry
[Image: see text] Easy scalable and eco-friendly syntheses of resorcin[5]arene, pyrogallol[5]arene, (2-nitro)resorcin[5]arene, (2-carboxyl)resorcin[5]arene, and resorcin[7]arene are presented and a wide range of upper-rim modifications is demonstrated. The macrocycles open the door toward expanding...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498192/ https://www.ncbi.nlm.nih.gov/pubmed/32820930 http://dx.doi.org/10.1021/acs.orglett.0c02357 |
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author | Chwastek, Monika Szumna, Agnieszka |
author_facet | Chwastek, Monika Szumna, Agnieszka |
author_sort | Chwastek, Monika |
collection | PubMed |
description | [Image: see text] Easy scalable and eco-friendly syntheses of resorcin[5]arene, pyrogallol[5]arene, (2-nitro)resorcin[5]arene, (2-carboxyl)resorcin[5]arene, and resorcin[7]arene are presented and a wide range of upper-rim modifications is demonstrated. The macrocycles open the door toward expanding the rich covalent and supramolecular chemistry of [4]arenes with analogues having unique 5-fold and 7-fold symmetry. |
format | Online Article Text |
id | pubmed-7498192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74981922020-09-18 Higher Analogues of Resorcinarenes and Pyrogallolarenes: Bricks for Supramolecular Chemistry Chwastek, Monika Szumna, Agnieszka Org Lett [Image: see text] Easy scalable and eco-friendly syntheses of resorcin[5]arene, pyrogallol[5]arene, (2-nitro)resorcin[5]arene, (2-carboxyl)resorcin[5]arene, and resorcin[7]arene are presented and a wide range of upper-rim modifications is demonstrated. The macrocycles open the door toward expanding the rich covalent and supramolecular chemistry of [4]arenes with analogues having unique 5-fold and 7-fold symmetry. American Chemical Society 2020-08-21 2020-09-04 /pmc/articles/PMC7498192/ /pubmed/32820930 http://dx.doi.org/10.1021/acs.orglett.0c02357 Text en Copyright © 2020 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 | Chwastek, Monika Szumna, Agnieszka Higher Analogues of Resorcinarenes and Pyrogallolarenes: Bricks for Supramolecular Chemistry |
title | Higher Analogues of Resorcinarenes and Pyrogallolarenes:
Bricks for Supramolecular
Chemistry |
title_full | Higher Analogues of Resorcinarenes and Pyrogallolarenes:
Bricks for Supramolecular
Chemistry |
title_fullStr | Higher Analogues of Resorcinarenes and Pyrogallolarenes:
Bricks for Supramolecular
Chemistry |
title_full_unstemmed | Higher Analogues of Resorcinarenes and Pyrogallolarenes:
Bricks for Supramolecular
Chemistry |
title_short | Higher Analogues of Resorcinarenes and Pyrogallolarenes:
Bricks for Supramolecular
Chemistry |
title_sort | higher analogues of resorcinarenes and pyrogallolarenes:
bricks for supramolecular
chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498192/ https://www.ncbi.nlm.nih.gov/pubmed/32820930 http://dx.doi.org/10.1021/acs.orglett.0c02357 |
work_keys_str_mv | AT chwastekmonika higheranaloguesofresorcinarenesandpyrogallolarenesbricksforsupramolecularchemistry AT szumnaagnieszka higheranaloguesofresorcinarenesandpyrogallolarenesbricksforsupramolecularchemistry |