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α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds

This minireview aims to cover the developments of the last few years in the design of reagents able to accomplish the umpolung of the azomethine carbon in diazo compounds namely, α-diazo-λ(3)-iodanes and α-diazo sulfonium salts. Specifically, the routes available for their preparation and a classifi...

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Detalles Bibliográficos
Autores principales: Timmann, Sven, Alcarazo, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297868/
https://www.ncbi.nlm.nih.gov/pubmed/37278355
http://dx.doi.org/10.1039/d3cc01620j
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author Timmann, Sven
Alcarazo, Manuel
author_facet Timmann, Sven
Alcarazo, Manuel
author_sort Timmann, Sven
collection PubMed
description This minireview aims to cover the developments of the last few years in the design of reagents able to accomplish the umpolung of the azomethine carbon in diazo compounds namely, α-diazo-λ(3)-iodanes and α-diazo sulfonium salts. Specifically, the routes available for their preparation and a classification of their unique reactivity patterns (either acting as equivalents of carbene-radical or carbene-carbocation synthons) are discussed. We also present a detailed overview of the synthetic utility of such species and, when possible, a critical comparation their reactivity and properties.
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spelling pubmed-102978682023-06-28 α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds Timmann, Sven Alcarazo, Manuel Chem Commun (Camb) Chemistry This minireview aims to cover the developments of the last few years in the design of reagents able to accomplish the umpolung of the azomethine carbon in diazo compounds namely, α-diazo-λ(3)-iodanes and α-diazo sulfonium salts. Specifically, the routes available for their preparation and a classification of their unique reactivity patterns (either acting as equivalents of carbene-radical or carbene-carbocation synthons) are discussed. We also present a detailed overview of the synthetic utility of such species and, when possible, a critical comparation their reactivity and properties. The Royal Society of Chemistry 2023-06-06 /pmc/articles/PMC10297868/ /pubmed/37278355 http://dx.doi.org/10.1039/d3cc01620j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Timmann, Sven
Alcarazo, Manuel
α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds
title α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds
title_full α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds
title_fullStr α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds
title_full_unstemmed α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds
title_short α-Diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds
title_sort α-diazo-λ(3)-iodanes and α-diazo sulfonium salts: the umpolung of diazo compounds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297868/
https://www.ncbi.nlm.nih.gov/pubmed/37278355
http://dx.doi.org/10.1039/d3cc01620j
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