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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...

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Detalles Bibliográficos
Autores principales: O’Connell, Kieron M G, Díaz-Gavilán, Monica, Galloway, Warren R J D, Spring, David R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
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.
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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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