Stereoselective synthesis of carbocyclic analogues of the nucleoside Q precursor (PreQ0)

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Abstract

A convergent and stereoselective synthesis of chiral cyclopentyl- and cyclohexylamine derivatives of nucleoside Q precursor (PreQ0) has been accomplished. This synthetic route allows for an efficient preparation of 4-substituted analogues with interesting three-dimensional character, including chiral cyclopentane-1,2-diol and -1,2,3-triol derivatives. This unusual substitution pattern provides a useful starting point for the discovery of novel bioactive molecules. © 2014 Llona-Minguez and Mackay.

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Llona-Minguez, S., & Mackay, S. P. (2014). Stereoselective synthesis of carbocyclic analogues of the nucleoside Q precursor (PreQ0). Beilstein Journal of Organic Chemistry, 10, 1333–1338. https://doi.org/10.3762/bjoc.10.135

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