| Literature DB >> 25600406 |
Philip Craven1, Anthony Aimon1, Mark Dow1, Nicolas Fleury-Bregeot2, Rachel Guilleux2, Remy Morgentin2, Didier Roche2, Tuomo Kalliokoski3, Richard Foster4, Stephen P Marsden1, Adam Nelson5.
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.Entities:
Keywords: Alkaloid; Aminoarylation; Cycloaddition; Small molecule libraries
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Year: 2014 PMID: 25600406 DOI: 10.1016/j.bmc.2014.12.048
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641