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A surprising new route to 4-nitro-3-phenylisoxazole
A one-pot synthesis of 4-nitro-3-phenylisoxazole has been carried out by treatment of cinnamyl alcohol dissolved in acetic acid with sodium nitrite; in addition, 4-phenyl-3-furoxanmethanol was obtained in 40% yield.
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2919271/ https://www.ncbi.nlm.nih.gov/pubmed/20703384 http://dx.doi.org/10.3762/bjoc.6.68 |
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author | Hopf, Henning Mourad, Aboul-fetouh E Jones, Peter G |
author_facet | Hopf, Henning Mourad, Aboul-fetouh E Jones, Peter G |
author_sort | Hopf, Henning |
collection | PubMed |
description | A one-pot synthesis of 4-nitro-3-phenylisoxazole has been carried out by treatment of cinnamyl alcohol dissolved in acetic acid with sodium nitrite; in addition, 4-phenyl-3-furoxanmethanol was obtained in 40% yield. |
format | Text |
id | pubmed-2919271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-29192712010-08-11 A surprising new route to 4-nitro-3-phenylisoxazole Hopf, Henning Mourad, Aboul-fetouh E Jones, Peter G Beilstein J Org Chem Preliminary Communication A one-pot synthesis of 4-nitro-3-phenylisoxazole has been carried out by treatment of cinnamyl alcohol dissolved in acetic acid with sodium nitrite; in addition, 4-phenyl-3-furoxanmethanol was obtained in 40% yield. Beilstein-Institut 2010-06-23 /pmc/articles/PMC2919271/ /pubmed/20703384 http://dx.doi.org/10.3762/bjoc.6.68 Text en Copyright © 2010, Hopf 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 | Preliminary Communication Hopf, Henning Mourad, Aboul-fetouh E Jones, Peter G A surprising new route to 4-nitro-3-phenylisoxazole |
title | A surprising new route to 4-nitro-3-phenylisoxazole |
title_full | A surprising new route to 4-nitro-3-phenylisoxazole |
title_fullStr | A surprising new route to 4-nitro-3-phenylisoxazole |
title_full_unstemmed | A surprising new route to 4-nitro-3-phenylisoxazole |
title_short | A surprising new route to 4-nitro-3-phenylisoxazole |
title_sort | surprising new route to 4-nitro-3-phenylisoxazole |
topic | Preliminary Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2919271/ https://www.ncbi.nlm.nih.gov/pubmed/20703384 http://dx.doi.org/10.3762/bjoc.6.68 |
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