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Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor®
A simple and practical protocol for the synthesis of 3-selanyl-benzo[b]furans mediated by the SelectFluor® reagent was developed. This novel methodology provided a greener alternative to generate 3-substituted-benzo[b]furans via a metal-free procedure under mild conditions. The intramolecular cycliz...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051628/ https://www.ncbi.nlm.nih.gov/pubmed/35498450 http://dx.doi.org/10.1039/d0ra01907k |
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author | Diem Ferreira Xavier, Maurício Carpe Andia Sandagorda, Eduardo Martarelo Santos Neto, José Sebastião Schumacher, Ricardo Frederico Silva, Márcio Santos |
author_facet | Diem Ferreira Xavier, Maurício Carpe Andia Sandagorda, Eduardo Martarelo Santos Neto, José Sebastião Schumacher, Ricardo Frederico Silva, Márcio Santos |
author_sort | Diem Ferreira Xavier, Maurício Carpe |
collection | PubMed |
description | A simple and practical protocol for the synthesis of 3-selanyl-benzo[b]furans mediated by the SelectFluor® reagent was developed. This novel methodology provided a greener alternative to generate 3-substituted-benzo[b]furans via a metal-free procedure under mild conditions. The intramolecular cyclization reaction was carried out employing an electrophilic selenium species generated in situ through the reaction between SelectFluor® and organic diselenides. The formation of this electrophilic selenium species (RSe-F) was confirmed by heteronuclear NMR spectroscopy, and its reactivity was explored. |
format | Online Article Text |
id | pubmed-9051628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90516282022-04-29 Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor® Diem Ferreira Xavier, Maurício Carpe Andia Sandagorda, Eduardo Martarelo Santos Neto, José Sebastião Schumacher, Ricardo Frederico Silva, Márcio Santos RSC Adv Chemistry A simple and practical protocol for the synthesis of 3-selanyl-benzo[b]furans mediated by the SelectFluor® reagent was developed. This novel methodology provided a greener alternative to generate 3-substituted-benzo[b]furans via a metal-free procedure under mild conditions. The intramolecular cyclization reaction was carried out employing an electrophilic selenium species generated in situ through the reaction between SelectFluor® and organic diselenides. The formation of this electrophilic selenium species (RSe-F) was confirmed by heteronuclear NMR spectroscopy, and its reactivity was explored. The Royal Society of Chemistry 2020-04-07 /pmc/articles/PMC9051628/ /pubmed/35498450 http://dx.doi.org/10.1039/d0ra01907k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Diem Ferreira Xavier, Maurício Carpe Andia Sandagorda, Eduardo Martarelo Santos Neto, José Sebastião Schumacher, Ricardo Frederico Silva, Márcio Santos Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor® |
title | Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor® |
title_full | Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor® |
title_fullStr | Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor® |
title_full_unstemmed | Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor® |
title_short | Synthesis of 3-selanylbenzo[b]furans promoted by SelectFluor® |
title_sort | synthesis of 3-selanylbenzo[b]furans promoted by selectfluor® |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051628/ https://www.ncbi.nlm.nih.gov/pubmed/35498450 http://dx.doi.org/10.1039/d0ra01907k |
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