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Synthesis of spirocyclic scaffolds using hypervalent iodine reagents

Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Various synthetically and biologically important scaffol...

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Autores principales: Singh, Fateh V, Kole, Priyanka B, Mangaonkar, Saeesh R, Shetgaonkar, Samata E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071689/
https://www.ncbi.nlm.nih.gov/pubmed/30112083
http://dx.doi.org/10.3762/bjoc.14.152
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author Singh, Fateh V
Kole, Priyanka B
Mangaonkar, Saeesh R
Shetgaonkar, Samata E
author_facet Singh, Fateh V
Kole, Priyanka B
Mangaonkar, Saeesh R
Shetgaonkar, Samata E
author_sort Singh, Fateh V
collection PubMed
description Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Various synthetically and biologically important scaffolds have been developed using hypervalent iodine reagents either in stoichiometric or catalytic amounts. In addition, hypervalent iodine reagents have been employed for the synthesis of spirocyclic scaffolds via dearomatization processes. In this review, various approaches for the synthesis of spirocyclic scaffolds using hypervalent iodine reagents are covered including their stereoselective synthesis. Additionally, the applications of these reagents in natural product synthesis are also covered.
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spelling pubmed-60716892018-08-15 Synthesis of spirocyclic scaffolds using hypervalent iodine reagents Singh, Fateh V Kole, Priyanka B Mangaonkar, Saeesh R Shetgaonkar, Samata E Beilstein J Org Chem Review Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Various synthetically and biologically important scaffolds have been developed using hypervalent iodine reagents either in stoichiometric or catalytic amounts. In addition, hypervalent iodine reagents have been employed for the synthesis of spirocyclic scaffolds via dearomatization processes. In this review, various approaches for the synthesis of spirocyclic scaffolds using hypervalent iodine reagents are covered including their stereoselective synthesis. Additionally, the applications of these reagents in natural product synthesis are also covered. Beilstein-Institut 2018-07-17 /pmc/articles/PMC6071689/ /pubmed/30112083 http://dx.doi.org/10.3762/bjoc.14.152 Text en Copyright © 2018, Singh 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). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Singh, Fateh V
Kole, Priyanka B
Mangaonkar, Saeesh R
Shetgaonkar, Samata E
Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
title Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
title_full Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
title_fullStr Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
title_full_unstemmed Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
title_short Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
title_sort synthesis of spirocyclic scaffolds using hypervalent iodine reagents
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071689/
https://www.ncbi.nlm.nih.gov/pubmed/30112083
http://dx.doi.org/10.3762/bjoc.14.152
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