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Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction
We have developed a catalytic synthetic method to prepare phenoxasilins. A borane-catalyzed double sila-Friedel–Crafts reaction between amino group-containing diaryl ethers and dihydrosilanes can be used to prepare a variety of phenoxasilin derivatives in good to excellent yields. The optimized reac...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113548/ https://www.ncbi.nlm.nih.gov/pubmed/32273904 http://dx.doi.org/10.3762/bjoc.16.39 |
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author | Dong, Yafang Sakai, Masahiko Fuji, Kazuto Sekine, Kohei Kuninobu, Yoichiro |
author_facet | Dong, Yafang Sakai, Masahiko Fuji, Kazuto Sekine, Kohei Kuninobu, Yoichiro |
author_sort | Dong, Yafang |
collection | PubMed |
description | We have developed a catalytic synthetic method to prepare phenoxasilins. A borane-catalyzed double sila-Friedel–Crafts reaction between amino group-containing diaryl ethers and dihydrosilanes can be used to prepare a variety of phenoxasilin derivatives in good to excellent yields. The optimized reaction conditions were also applicable for diaryl thioethers to afford their corresponding six-membered silacyclic products. The gram-scale synthesis of a representative bis(dimethylamino)phenoxasilin and the transformation of its amino groups have also been demonstrated. |
format | Online Article Text |
id | pubmed-7113548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-71135482020-04-09 Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction Dong, Yafang Sakai, Masahiko Fuji, Kazuto Sekine, Kohei Kuninobu, Yoichiro Beilstein J Org Chem Letter We have developed a catalytic synthetic method to prepare phenoxasilins. A borane-catalyzed double sila-Friedel–Crafts reaction between amino group-containing diaryl ethers and dihydrosilanes can be used to prepare a variety of phenoxasilin derivatives in good to excellent yields. The optimized reaction conditions were also applicable for diaryl thioethers to afford their corresponding six-membered silacyclic products. The gram-scale synthesis of a representative bis(dimethylamino)phenoxasilin and the transformation of its amino groups have also been demonstrated. Beilstein-Institut 2020-03-17 /pmc/articles/PMC7113548/ /pubmed/32273904 http://dx.doi.org/10.3762/bjoc.16.39 Text en Copyright © 2020, Dong et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Letter Dong, Yafang Sakai, Masahiko Fuji, Kazuto Sekine, Kohei Kuninobu, Yoichiro Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction |
title | Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction |
title_full | Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction |
title_fullStr | Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction |
title_full_unstemmed | Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction |
title_short | Synthesis of six-membered silacycles by borane-catalyzed double sila-Friedel–Crafts reaction |
title_sort | synthesis of six-membered silacycles by borane-catalyzed double sila-friedel–crafts reaction |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113548/ https://www.ncbi.nlm.nih.gov/pubmed/32273904 http://dx.doi.org/10.3762/bjoc.16.39 |
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