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Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof
Lithium anions derived from O-carbonate-protected cyanohydrins undergo conjugate addition to cycloalkenones with the concomitant transfer of the alkoxycarbonyl group to produce tricarbonyl compounds. These products offer numerous possibilities for further elaboration. The synthetic potential of the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042245/ https://www.ncbi.nlm.nih.gov/pubmed/35497560 http://dx.doi.org/10.1039/d1ra05187c |
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author | Madroñero, Diego Mujica-Martinez, Cesar A. Vázquez, Alfredo |
author_facet | Madroñero, Diego Mujica-Martinez, Cesar A. Vázquez, Alfredo |
author_sort | Madroñero, Diego |
collection | PubMed |
description | Lithium anions derived from O-carbonate-protected cyanohydrins undergo conjugate addition to cycloalkenones with the concomitant transfer of the alkoxycarbonyl group to produce tricarbonyl compounds. These products offer numerous possibilities for further elaboration. The synthetic potential of the cascade products was demonstrated by forming bicyclic and tricyclic systems through intramolecular condensation reactions. |
format | Online Article Text |
id | pubmed-9042245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90422452022-04-28 Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof Madroñero, Diego Mujica-Martinez, Cesar A. Vázquez, Alfredo RSC Adv Chemistry Lithium anions derived from O-carbonate-protected cyanohydrins undergo conjugate addition to cycloalkenones with the concomitant transfer of the alkoxycarbonyl group to produce tricarbonyl compounds. These products offer numerous possibilities for further elaboration. The synthetic potential of the cascade products was demonstrated by forming bicyclic and tricyclic systems through intramolecular condensation reactions. The Royal Society of Chemistry 2021-10-11 /pmc/articles/PMC9042245/ /pubmed/35497560 http://dx.doi.org/10.1039/d1ra05187c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Madroñero, Diego Mujica-Martinez, Cesar A. Vázquez, Alfredo Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof |
title | Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof |
title_full | Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof |
title_fullStr | Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof |
title_full_unstemmed | Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof |
title_short | Consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof |
title_sort | consecutive reactions to construct tricarbonyl compounds and synthetic applications thereof |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042245/ https://www.ncbi.nlm.nih.gov/pubmed/35497560 http://dx.doi.org/10.1039/d1ra05187c |
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