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Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides
A novel method of photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides has been developed. Although the arylation reactions with triarylbismuthines are usually catalyzed by transition-metal complexes, the present arylation of diaryl diselenides with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701414/ https://www.ncbi.nlm.nih.gov/pubmed/23843906 http://dx.doi.org/10.3762/bjoc.9.127 |
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author | Kobiki, Yohsuke Kawaguchi, Shin-ichi Ohe, Takashi Ogawa, Akiya |
author_facet | Kobiki, Yohsuke Kawaguchi, Shin-ichi Ohe, Takashi Ogawa, Akiya |
author_sort | Kobiki, Yohsuke |
collection | PubMed |
description | A novel method of photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides has been developed. Although the arylation reactions with triarylbismuthines are usually catalyzed by transition-metal complexes, the present arylation of diaryl diselenides with triarylbismuthines proceeds upon photoirradiation in the absence of transition-metal catalysts. A variety of unsymmetrical diaryl selenides can be conveniently prepared by using this arylation method. |
format | Online Article Text |
id | pubmed-3701414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-37014142013-07-10 Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides Kobiki, Yohsuke Kawaguchi, Shin-ichi Ohe, Takashi Ogawa, Akiya Beilstein J Org Chem Letter A novel method of photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides has been developed. Although the arylation reactions with triarylbismuthines are usually catalyzed by transition-metal complexes, the present arylation of diaryl diselenides with triarylbismuthines proceeds upon photoirradiation in the absence of transition-metal catalysts. A variety of unsymmetrical diaryl selenides can be conveniently prepared by using this arylation method. Beilstein-Institut 2013-06-13 /pmc/articles/PMC3701414/ /pubmed/23843906 http://dx.doi.org/10.3762/bjoc.9.127 Text en Copyright © 2013, Kobiki et al. https://creativecommons.org/licenses/by/2.0https://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/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Letter Kobiki, Yohsuke Kawaguchi, Shin-ichi Ohe, Takashi Ogawa, Akiya Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides |
title | Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides |
title_full | Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides |
title_fullStr | Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides |
title_full_unstemmed | Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides |
title_short | Photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides |
title_sort | photoinduced synthesis of unsymmetrical diaryl selenides from triarylbismuthines and diaryl diselenides |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701414/ https://www.ncbi.nlm.nih.gov/pubmed/23843906 http://dx.doi.org/10.3762/bjoc.9.127 |
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