Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1785063975567753216 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10297868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT timmannsven adiazol3iodanesandadiazosulfoniumsaltstheumpolungofdiazocompounds AT alcarazomanuel adiazol3iodanesandadiazosulfoniumsaltstheumpolungofdiazocompounds |