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Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines
A [3 + 3] annelation of enantiomerically pure aziridine 7 provides the functionalised piperidine 8 that can be elaborated to the indolizidine skeleton in only 4 steps with good stereocontrol.
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810302/ https://www.ncbi.nlm.nih.gov/pubmed/17288604 http://dx.doi.org/10.1186/1860-5397-3-8 |
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author | Provoost, Olivier Y Hazelwood, Andrew J Harrity, Joseph P A |
author_facet | Provoost, Olivier Y Hazelwood, Andrew J Harrity, Joseph P A |
author_sort | Provoost, Olivier Y |
collection | PubMed |
description | A [3 + 3] annelation of enantiomerically pure aziridine 7 provides the functionalised piperidine 8 that can be elaborated to the indolizidine skeleton in only 4 steps with good stereocontrol. |
format | Text |
id | pubmed-1810302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-18103022007-03-06 Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines Provoost, Olivier Y Hazelwood, Andrew J Harrity, Joseph P A Beilstein J Org Chem Preliminary Communication A [3 + 3] annelation of enantiomerically pure aziridine 7 provides the functionalised piperidine 8 that can be elaborated to the indolizidine skeleton in only 4 steps with good stereocontrol. Beilstein-Institut 2007-02-08 /pmc/articles/PMC1810302/ /pubmed/17288604 http://dx.doi.org/10.1186/1860-5397-3-8 Text en Copyright © 2007, Provoost 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 | Preliminary Communication Provoost, Olivier Y Hazelwood, Andrew J Harrity, Joseph P A Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines |
title | Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines |
title_full | Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines |
title_fullStr | Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines |
title_full_unstemmed | Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines |
title_short | Pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines |
title_sort | pd-catalysed [3 + 3] annelations in the stereoselective synthesis of indolizidines |
topic | Preliminary Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810302/ https://www.ncbi.nlm.nih.gov/pubmed/17288604 http://dx.doi.org/10.1186/1860-5397-3-8 |
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