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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...

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Autores principales: Diem Ferreira Xavier, Maurício Carpe, Andia Sandagorda, Eduardo Martarelo, Santos Neto, José Sebastião, Schumacher, Ricardo Frederico, Silva, Márcio Santos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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