Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hussain, Zakir, Hopf, Henning, Ayub, Khurshid, Eichhorn, S Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
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
_version_ 1782237249199407104
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
work_keys_str_mv AT hussainzakir synthesisof26disubstitutedtetrahydroazulenederivatives
AT hopfhenning synthesisof26disubstitutedtetrahydroazulenederivatives
AT ayubkhurshid synthesisof26disubstitutedtetrahydroazulenederivatives
AT eichhornsholger synthesisof26disubstitutedtetrahydroazulenederivatives