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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...

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Detalles Bibliográficos
Autores principales: Dong, Yafang, Sakai, Masahiko, Fuji, Kazuto, Sekine, Kohei, Kuninobu, Yoichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
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.
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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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