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dc.contributor.authorReekie, Tristan A.
dc.contributor.authorWilliams, Craig M.
dc.contributor.authorRendina, Louis M.
dc.contributor.authorKassiou, Michael
dc.date.accessioned2021-03-31T06:01:42Z
dc.date.available2021-03-31T06:01:42Z
dc.date.issued2019en_AU
dc.identifier.urihttps://hdl.handle.net/2123/24777
dc.description.abstractCubane is a highly strained saturated hydrocarbon system that has historically been of interest in theoretical organic chemistry. More recently it has become a molecule of interest for biological applications due to its inherent stability and limited toxicity. Of greater significance is the ability to potentially functionalize cubane at each of its carbon atoms, providing complex biologically active molecules with unique spatial arrangements for probing active sites. These characteristics have led to an increased use of cubane in pharmaceutically relevant molecules. In this Perspective we describe synthetic methodology for accessing a range of functionalized cubanes and their applications in pharmaceuticals. We also provide some perspectives on challenges and future directions in the advancement of this field.en_AU
dc.language.isoenen_AU
dc.publisherACS Publicationsen_AU
dc.relation.ispartofJournal of Medicinal Chemistryen_AU
dc.rightsCopyright All Rights Reserveden_AU
dc.subjectcubaneen_AU
dc.subjectmedicinal chemistryen_AU
dc.titleCubanes in Medicinal Chemistryen_AU
dc.typeArticleen_AU
dc.subject.asrc03 Chemical Sciencesen_AU
dc.subject.asrc0304 Medicinal and Biomolecular Chemistryen_AU
dc.subject.asrc0305 Organic Chemistryen_AU
dc.identifier.doi10.1021/acs.jmedchem.8b00888
dc.relation.arcFT110100851
dc.relation.arcDP110104237
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume62en_AU
usyd.citation.issue3en_AU
usyd.citation.spage1078en_AU
usyd.citation.epage1095en_AU
workflow.metadata.onlyNoen_AU


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