Stereoselective synthesis of carbocyclic analogues of the nucleoside Q precursor (PreQ0)
Llona-Minguez, S. and MacKay, S.P. (2014) Stereoselective synthesis of carbocyclic analogues of the nucleoside Q precursor (PreQ0). Beilstein Journal of Organic Chemistry, 10. pp. 1333-1338. ISSN 1860-5397 (https://doi.org/10.3762/bjoc.10.135)
Preview |
Text.
Filename: Llona_Minguez_Mackay_BJOC2014_stereoselective_synthesis_of_carbocyclic_analogues.pdf
Final Published Version License: Download (287kB)| Preview |
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.
ORCID iDs
Llona-Minguez, S. and MacKay, S.P. ORCID: https://orcid.org/0000-0001-8000-6557;-
-
Item type: Article ID code: 53022 Dates: DateEvent11 June 2014PublishedSubjects: Medicine > Pharmacy and materia medica Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 14 May 2015 15:18 Last modified: 11 Nov 2024 11:05 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/53022