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Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis

Most of the polyvalent organoiodine compounds derive from iodoarenes, which are released in stoichiometric amounts in any reaction mediated by λ(3)- or λ(5)-iodanes. In parallel to the development of solid-supported reagents or reactions catalytic in iodine, a third strategy has emerged to address t...

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Detalles Bibliográficos
Autores principales: Grelier, Gwendal, Darses, Benjamin, Dauban, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037006/
https://www.ncbi.nlm.nih.gov/pubmed/30013678
http://dx.doi.org/10.3762/bjoc.14.128
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author Grelier, Gwendal
Darses, Benjamin
Dauban, Philippe
author_facet Grelier, Gwendal
Darses, Benjamin
Dauban, Philippe
author_sort Grelier, Gwendal
collection PubMed
description Most of the polyvalent organoiodine compounds derive from iodoarenes, which are released in stoichiometric amounts in any reaction mediated by λ(3)- or λ(5)-iodanes. In parallel to the development of solid-supported reagents or reactions catalytic in iodine, a third strategy has emerged to address this issue in terms of sustainability. The atom-economy of transformations involving stoichiometric amounts of λ(3)- or λ(5)-iodanes, thus, has been improved by designing tandem reactions that allows for incorporating the aryl motif into the products through a subsequent one-pot nucleophilic addition or catalytic coupling reaction. This review summarizes the main achievements reported in this area.
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spelling pubmed-60370062018-07-16 Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis Grelier, Gwendal Darses, Benjamin Dauban, Philippe Beilstein J Org Chem Review Most of the polyvalent organoiodine compounds derive from iodoarenes, which are released in stoichiometric amounts in any reaction mediated by λ(3)- or λ(5)-iodanes. In parallel to the development of solid-supported reagents or reactions catalytic in iodine, a third strategy has emerged to address this issue in terms of sustainability. The atom-economy of transformations involving stoichiometric amounts of λ(3)- or λ(5)-iodanes, thus, has been improved by designing tandem reactions that allows for incorporating the aryl motif into the products through a subsequent one-pot nucleophilic addition or catalytic coupling reaction. This review summarizes the main achievements reported in this area. Beilstein-Institut 2018-06-21 /pmc/articles/PMC6037006/ /pubmed/30013678 http://dx.doi.org/10.3762/bjoc.14.128 Text en Copyright © 2018, Grelier 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), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Grelier, Gwendal
Darses, Benjamin
Dauban, Philippe
Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis
title Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis
title_full Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis
title_fullStr Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis
title_full_unstemmed Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis
title_short Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis
title_sort hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037006/
https://www.ncbi.nlm.nih.gov/pubmed/30013678
http://dx.doi.org/10.3762/bjoc.14.128
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