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Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds
Two-directional synthesis represents an ideal strategy for the rapid elaboration of simple starting materials and their subsequent transformation into complex molecular architectures. As such, it is becoming recognised as an enabling technology for diversity-oriented synthesis. Herein, we provide a...
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/PMC3388873/ https://www.ncbi.nlm.nih.gov/pubmed/23015833 http://dx.doi.org/10.3762/bjoc.8.95 |
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author | O’Connell, Kieron M G Díaz-Gavilán, Monica Galloway, Warren R J D Spring, David R |
author_facet | O’Connell, Kieron M G Díaz-Gavilán, Monica Galloway, Warren R J D Spring, David R |
author_sort | O’Connell, Kieron M G |
collection | PubMed |
description | Two-directional synthesis represents an ideal strategy for the rapid elaboration of simple starting materials and their subsequent transformation into complex molecular architectures. As such, it is becoming recognised as an enabling technology for diversity-oriented synthesis. Herein, we provide a thorough account of our work combining two-directional synthesis with diversity-oriented synthesis, with particular reference to the synthesis of polycyclic alkaloid scaffolds. |
format | Online Article Text |
id | pubmed-3388873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-33888732012-09-26 Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds O’Connell, Kieron M G Díaz-Gavilán, Monica Galloway, Warren R J D Spring, David R Beilstein J Org Chem Full Research Paper Two-directional synthesis represents an ideal strategy for the rapid elaboration of simple starting materials and their subsequent transformation into complex molecular architectures. As such, it is becoming recognised as an enabling technology for diversity-oriented synthesis. Herein, we provide a thorough account of our work combining two-directional synthesis with diversity-oriented synthesis, with particular reference to the synthesis of polycyclic alkaloid scaffolds. Beilstein-Institut 2012-06-06 /pmc/articles/PMC3388873/ /pubmed/23015833 http://dx.doi.org/10.3762/bjoc.8.95 Text en Copyright © 2012, O’Connell 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 O’Connell, Kieron M G Díaz-Gavilán, Monica Galloway, Warren R J D Spring, David R Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds |
title | Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds |
title_full | Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds |
title_fullStr | Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds |
title_full_unstemmed | Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds |
title_short | Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds |
title_sort | two-directional synthesis as a tool for diversity-oriented synthesis: synthesis of alkaloid scaffolds |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388873/ https://www.ncbi.nlm.nih.gov/pubmed/23015833 http://dx.doi.org/10.3762/bjoc.8.95 |
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