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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...

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Autores principales: Mandal, Sumana, Chaudhari, Raju D, Biswas, Goutam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2021
Materias:
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.
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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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