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Preparation and isolation of isobenzofuran
The synthesis, isolation and characterization of isobenzofuran are described in this publication. Isobenzofuran is of general interest in synthetic and physical organic chemistry because it is one of the most reactive dienes known. A number of synthetic pathways have been published which all suffer...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753151/ https://www.ncbi.nlm.nih.gov/pubmed/30018664 http://dx.doi.org/10.3762/bjoc.13.263 |
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author | Peters, Morten K Herges, Rainer |
author_facet | Peters, Morten K Herges, Rainer |
author_sort | Peters, Morten K |
collection | PubMed |
description | The synthesis, isolation and characterization of isobenzofuran are described in this publication. Isobenzofuran is of general interest in synthetic and physical organic chemistry because it is one of the most reactive dienes known. A number of synthetic pathways have been published which all suffer from disadvantages such as low yields and difficult purification. We present a synthetic pathway to prepare isobenzofuran in laboratory scale with high yields, from affordable, commercially available starting materials. |
format | Online Article Text |
id | pubmed-5753151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-57531512018-07-17 Preparation and isolation of isobenzofuran Peters, Morten K Herges, Rainer Beilstein J Org Chem Letter The synthesis, isolation and characterization of isobenzofuran are described in this publication. Isobenzofuran is of general interest in synthetic and physical organic chemistry because it is one of the most reactive dienes known. A number of synthetic pathways have been published which all suffer from disadvantages such as low yields and difficult purification. We present a synthetic pathway to prepare isobenzofuran in laboratory scale with high yields, from affordable, commercially available starting materials. Beilstein-Institut 2017-12-12 /pmc/articles/PMC5753151/ /pubmed/30018664 http://dx.doi.org/10.3762/bjoc.13.263 Text en Copyright © 2017, Peters and Herges 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), 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 Peters, Morten K Herges, Rainer Preparation and isolation of isobenzofuran |
title | Preparation and isolation of isobenzofuran |
title_full | Preparation and isolation of isobenzofuran |
title_fullStr | Preparation and isolation of isobenzofuran |
title_full_unstemmed | Preparation and isolation of isobenzofuran |
title_short | Preparation and isolation of isobenzofuran |
title_sort | preparation and isolation of isobenzofuran |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753151/ https://www.ncbi.nlm.nih.gov/pubmed/30018664 http://dx.doi.org/10.3762/bjoc.13.263 |
work_keys_str_mv | AT petersmortenk preparationandisolationofisobenzofuran AT hergesrainer preparationandisolationofisobenzofuran |