Craven, P orcid.org/0000-0002-7617-132X, Aimon, A, Dow, M et al. (8 more authors) (2015) Design, synthesis and decoration of molecular scaffolds for exploitation in the production of alkaloid-like libraries. Bioorganic and Medicinal Chemistry, 23 (11). pp. 2629-2635. ISSN 0968-0896
Abstract
The design, synthesis and decoration of six small molecule libraries is described. Each library was inspired by structures embedded in the framework of specific alkaloid natural products. The development of optimised syntheses of the required molecular scaffolds is described, in which reactions including Pd-catalysed aminoarylation and diplolar cycloadditions have been exploited as key steps. The synthesis of selected exemplar screening compounds is also described. In five cases, libraries were subsequently nominated for production on the basis of the scope and limitations of the validation work, as well as predicted molecular properties. In total, the research has led to the successful synthesis of >2500 novel alkaloid-like compounds for addition to the screening collection (the Joint European Compound Library, JECL) of the European Lead Factory.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Keywords: | Alkaloid; small molecule libraries; aminoarylation; cycloaddition |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) > Organic Chemistry (Leeds) The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 04 Feb 2015 10:40 |
Last Modified: | 20 Jun 2021 08:37 |
Published Version: | http://dx.doi.org/10.1016/j.bmc.2014.12.048 |
Status: | Published |
Publisher: | Elsevier |
Identification Number: | 10.1016/j.bmc.2014.12.048 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:83117 |