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Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds
The synthesis of complex cyclic compounds is extremely challenging for organic chemists. Many transition-metal-salt-mediated cyclizations are reported in literature. Hg(II) salts have been successfully employed in cyclizations to form complex heterocyclic and carbocyclic structures that are impossib...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450975/ https://www.ncbi.nlm.nih.gov/pubmed/34621398 http://dx.doi.org/10.3762/bjoc.17.153 |
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author | Mandal, Sumana Chaudhari, Raju D Biswas, Goutam |
author_facet | Mandal, Sumana Chaudhari, Raju D Biswas, Goutam |
author_sort | Mandal, Sumana |
collection | PubMed |
description | The synthesis of complex cyclic compounds is extremely challenging for organic chemists. Many transition-metal-salt-mediated cyclizations are reported in literature. Hg(II) salts have been successfully employed in cyclizations to form complex heterocyclic and carbocyclic structures that are impossible to synthesize with other transition metal salts. In this review, we have summarized cyclization reactions that are performed with Hg(II) salts. These salts are also successfully applied in stoichiometric or catalytic amounts to form complex cyclic structures and natural products. |
format | Online Article Text |
id | pubmed-8450975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-84509752021-10-06 Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds Mandal, Sumana Chaudhari, Raju D Biswas, Goutam Beilstein J Org Chem Review The synthesis of complex cyclic compounds is extremely challenging for organic chemists. Many transition-metal-salt-mediated cyclizations are reported in literature. Hg(II) salts have been successfully employed in cyclizations to form complex heterocyclic and carbocyclic structures that are impossible to synthesize with other transition metal salts. In this review, we have summarized cyclization reactions that are performed with Hg(II) salts. These salts are also successfully applied in stoichiometric or catalytic amounts to form complex cyclic structures and natural products. Beilstein-Institut 2021-09-09 /pmc/articles/PMC8450975/ /pubmed/34621398 http://dx.doi.org/10.3762/bjoc.17.153 Text en Copyright © 2021, Mandal et al. https://creativecommons.org/licenses/by/4.0/https://www.beilstein-journals.org/bjoc/terms/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms/terms) |
spellingShingle | Review Mandal, Sumana Chaudhari, Raju D Biswas, Goutam Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds |
title | Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds |
title_full | Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds |
title_fullStr | Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds |
title_full_unstemmed | Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds |
title_short | Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds |
title_sort | advances in mercury(ii)-salt-mediated cyclization reactions of unsaturated bonds |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450975/ https://www.ncbi.nlm.nih.gov/pubmed/34621398 http://dx.doi.org/10.3762/bjoc.17.153 |
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