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Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene
C(72)-Macrocyclic systems functionalized with nitroaryl and arylamino groups were synthesized from the bisdioxine diacid dichloride 1,3,5,7-tetra-tert-butyl-2,6,9-trioxabicyclo[3.3.1]nona-3,7-diene-4,8-dicarbonyl dichloride (3).
| 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/PMC3388861/ https://www.ncbi.nlm.nih.gov/pubmed/23015821 http://dx.doi.org/10.3762/bjoc.8.83 |
| _version_ | 1782237250584576000 |
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| author | Leber, Sabine Kollenz, Gert Wentrup, Curt |
| author_facet | Leber, Sabine Kollenz, Gert Wentrup, Curt |
| author_sort | Leber, Sabine |
| collection | PubMed |
| description | C(72)-Macrocyclic systems functionalized with nitroaryl and arylamino groups were synthesized from the bisdioxine diacid dichloride 1,3,5,7-tetra-tert-butyl-2,6,9-trioxabicyclo[3.3.1]nona-3,7-diene-4,8-dicarbonyl dichloride (3). |
| format | Online Article Text |
| id | pubmed-3388861 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2012 |
| publisher | Beilstein-Institut |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-33888612012-09-26 Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene Leber, Sabine Kollenz, Gert Wentrup, Curt Beilstein J Org Chem Full Research Paper C(72)-Macrocyclic systems functionalized with nitroaryl and arylamino groups were synthesized from the bisdioxine diacid dichloride 1,3,5,7-tetra-tert-butyl-2,6,9-trioxabicyclo[3.3.1]nona-3,7-diene-4,8-dicarbonyl dichloride (3). Beilstein-Institut 2012-05-15 /pmc/articles/PMC3388861/ /pubmed/23015821 http://dx.doi.org/10.3762/bjoc.8.83 Text en Copyright © 2012, Leber 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 Leber, Sabine Kollenz, Gert Wentrup, Curt Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene |
| title | Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene |
| title_full | Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene |
| title_fullStr | Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene |
| title_full_unstemmed | Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene |
| title_short | Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene |
| title_sort | synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene |
| topic | Full Research Paper |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388861/ https://www.ncbi.nlm.nih.gov/pubmed/23015821 http://dx.doi.org/10.3762/bjoc.8.83 |
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