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Synthetic Applications of Aziridinium Ions
Nonactivated aziridine with an electron-donating group at the ring nitrogen should be activated to an aziridinium ion prior to being converted to cyclic and acyclic nitrogen-containing molecules. This review describes ways to generate aziridinium ions and their utilization for synthetic purposes. Sp...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004105/ https://www.ncbi.nlm.nih.gov/pubmed/33809951 http://dx.doi.org/10.3390/molecules26061774 |
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author | Ranjith, Jala Ha, Hyun-Joon |
author_facet | Ranjith, Jala Ha, Hyun-Joon |
author_sort | Ranjith, Jala |
collection | PubMed |
description | Nonactivated aziridine with an electron-donating group at the ring nitrogen should be activated to an aziridinium ion prior to being converted to cyclic and acyclic nitrogen-containing molecules. This review describes ways to generate aziridinium ions and their utilization for synthetic purposes. Specifically, the intra- and intermolecular formation of aziridinium ions with proper electrophiles are classified, and their regio- and stereoselective transformations with nucleophiles are described on the basis of recent developments. |
format | Online Article Text |
id | pubmed-8004105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80041052021-03-28 Synthetic Applications of Aziridinium Ions Ranjith, Jala Ha, Hyun-Joon Molecules Review Nonactivated aziridine with an electron-donating group at the ring nitrogen should be activated to an aziridinium ion prior to being converted to cyclic and acyclic nitrogen-containing molecules. This review describes ways to generate aziridinium ions and their utilization for synthetic purposes. Specifically, the intra- and intermolecular formation of aziridinium ions with proper electrophiles are classified, and their regio- and stereoselective transformations with nucleophiles are described on the basis of recent developments. MDPI 2021-03-22 /pmc/articles/PMC8004105/ /pubmed/33809951 http://dx.doi.org/10.3390/molecules26061774 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ranjith, Jala Ha, Hyun-Joon Synthetic Applications of Aziridinium Ions |
title | Synthetic Applications of Aziridinium Ions |
title_full | Synthetic Applications of Aziridinium Ions |
title_fullStr | Synthetic Applications of Aziridinium Ions |
title_full_unstemmed | Synthetic Applications of Aziridinium Ions |
title_short | Synthetic Applications of Aziridinium Ions |
title_sort | synthetic applications of aziridinium ions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004105/ https://www.ncbi.nlm.nih.gov/pubmed/33809951 http://dx.doi.org/10.3390/molecules26061774 |
work_keys_str_mv | AT ranjithjala syntheticapplicationsofaziridiniumions AT hahyunjoon syntheticapplicationsofaziridiniumions |