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Synthesis of 2,6-disubstituted tetrahydroazulene derivatives
Synthesis of hydroazulene derivatives has been carried out through a ring-enlargement route by using carbene adduct intermediates. The protocol can be applied for the construction of functionalized hydroazulene skeletons as key components of many natural products as well as the core system of novel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388855/ https://www.ncbi.nlm.nih.gov/pubmed/23015815 http://dx.doi.org/10.3762/bjoc.8.77 |
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author | Hussain, Zakir Hopf, Henning Ayub, Khurshid Eichhorn, S Holger |
author_facet | Hussain, Zakir Hopf, Henning Ayub, Khurshid Eichhorn, S Holger |
author_sort | Hussain, Zakir |
collection | PubMed |
description | Synthesis of hydroazulene derivatives has been carried out through a ring-enlargement route by using carbene adduct intermediates. The protocol can be applied for the construction of functionalized hydroazulene skeletons as key components of many natural products as well as the core system of novel liquid-crystalline materials. |
format | Online Article Text |
id | pubmed-3388855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-33888552012-09-26 Synthesis of 2,6-disubstituted tetrahydroazulene derivatives Hussain, Zakir Hopf, Henning Ayub, Khurshid Eichhorn, S Holger Beilstein J Org Chem Full Research Paper Synthesis of hydroazulene derivatives has been carried out through a ring-enlargement route by using carbene adduct intermediates. The protocol can be applied for the construction of functionalized hydroazulene skeletons as key components of many natural products as well as the core system of novel liquid-crystalline materials. Beilstein-Institut 2012-05-04 /pmc/articles/PMC3388855/ /pubmed/23015815 http://dx.doi.org/10.3762/bjoc.8.77 Text en Copyright © 2012, Hussain 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 | Full Research Paper Hussain, Zakir Hopf, Henning Ayub, Khurshid Eichhorn, S Holger Synthesis of 2,6-disubstituted tetrahydroazulene derivatives |
title | Synthesis of 2,6-disubstituted tetrahydroazulene derivatives |
title_full | Synthesis of 2,6-disubstituted tetrahydroazulene derivatives |
title_fullStr | Synthesis of 2,6-disubstituted tetrahydroazulene derivatives |
title_full_unstemmed | Synthesis of 2,6-disubstituted tetrahydroazulene derivatives |
title_short | Synthesis of 2,6-disubstituted tetrahydroazulene derivatives |
title_sort | synthesis of 2,6-disubstituted tetrahydroazulene derivatives |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388855/ https://www.ncbi.nlm.nih.gov/pubmed/23015815 http://dx.doi.org/10.3762/bjoc.8.77 |
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