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Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers

Dimeric forms of norbornadiene and benzonorbornadiene were synthesized starting with known monobromide derivatives. The Diels–Alder cycloaddition reaction of dimers with TCNE and PTAD was investigated and new norbornenoid polycyclics were obtained. All compounds were characterized properly using NMR...

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Detalles Bibliográficos
Autores principales: Nişancı, Bilal, Dalkılıç, Erdin, Güney, Murat, Daştan, Arif
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2748719/
https://www.ncbi.nlm.nih.gov/pubmed/19777139
http://dx.doi.org/10.3762/bjoc.5.39
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author Nişancı, Bilal
Dalkılıç, Erdin
Güney, Murat
Daştan, Arif
author_facet Nişancı, Bilal
Dalkılıç, Erdin
Güney, Murat
Daştan, Arif
author_sort Nişancı, Bilal
collection PubMed
description Dimeric forms of norbornadiene and benzonorbornadiene were synthesized starting with known monobromide derivatives. The Diels–Alder cycloaddition reaction of dimers with TCNE and PTAD was investigated and new norbornenoid polycyclics were obtained. All compounds were characterized properly using NMR spectroscopy.
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spelling pubmed-27487192009-09-23 Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers Nişancı, Bilal Dalkılıç, Erdin Güney, Murat Daştan, Arif Beilstein J Org Chem Full Research Paper Dimeric forms of norbornadiene and benzonorbornadiene were synthesized starting with known monobromide derivatives. The Diels–Alder cycloaddition reaction of dimers with TCNE and PTAD was investigated and new norbornenoid polycyclics were obtained. All compounds were characterized properly using NMR spectroscopy. Beilstein-Institut 2009-08-11 /pmc/articles/PMC2748719/ /pubmed/19777139 http://dx.doi.org/10.3762/bjoc.5.39 Text en Copyright © 2009, Nişancı 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
Nişancı, Bilal
Dalkılıç, Erdin
Güney, Murat
Daştan, Arif
Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
title Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
title_full Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
title_fullStr Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
title_full_unstemmed Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
title_short Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
title_sort synthesis and diels–alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2748719/
https://www.ncbi.nlm.nih.gov/pubmed/19777139
http://dx.doi.org/10.3762/bjoc.5.39
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