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Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence
We have developed an efficient synthetic strategy to assemble C(3)-symmetric molecules containing propellane moieties as end groups and a benzene ring as a central core. The synthesis of these C(3)-symmetric molecules involves simple starting materials. Our approach to C(3)-symmetric compounds relie...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204777/ https://www.ncbi.nlm.nih.gov/pubmed/30410614 http://dx.doi.org/10.3762/bjoc.14.230 |
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author | Kotha, Sambasivarao Todeti, Saidulu Aswar, Vikas R |
author_facet | Kotha, Sambasivarao Todeti, Saidulu Aswar, Vikas R |
author_sort | Kotha, Sambasivarao |
collection | PubMed |
description | We have developed an efficient synthetic strategy to assemble C(3)-symmetric molecules containing propellane moieties as end groups and a benzene ring as a central core. The synthesis of these C(3)-symmetric molecules involves simple starting materials. Our approach to C(3)-symmetric compounds relies on a Diels–Alder reaction, cyclotrimerization and ring-closing metathesis as key steps. |
format | Online Article Text |
id | pubmed-6204777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-62047772018-11-08 Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence Kotha, Sambasivarao Todeti, Saidulu Aswar, Vikas R Beilstein J Org Chem Full Research Paper We have developed an efficient synthetic strategy to assemble C(3)-symmetric molecules containing propellane moieties as end groups and a benzene ring as a central core. The synthesis of these C(3)-symmetric molecules involves simple starting materials. Our approach to C(3)-symmetric compounds relies on a Diels–Alder reaction, cyclotrimerization and ring-closing metathesis as key steps. Beilstein-Institut 2018-10-01 /pmc/articles/PMC6204777/ /pubmed/30410614 http://dx.doi.org/10.3762/bjoc.14.230 Text en Copyright © 2018, Kotha et al. 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). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. 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 Kotha, Sambasivarao Todeti, Saidulu Aswar, Vikas R Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence |
title | Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence |
title_full | Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence |
title_fullStr | Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence |
title_full_unstemmed | Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence |
title_short | Design and synthesis of C(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence |
title_sort | design and synthesis of c(3)-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204777/ https://www.ncbi.nlm.nih.gov/pubmed/30410614 http://dx.doi.org/10.3762/bjoc.14.230 |
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