Publication | Closed Access
Total Synthesis of Gabosines
29
Citations
47
References
2012
Year
Medicinal ChemistryBioorganic ChemistryCyclohexenone CoresBiochemistryHeterocyclicNatural SciencesDiversity-oriented SynthesisTotal SynthesisOrganic ChemistrySecondary MetabolitesHeterocycle ChemistrySynthesis MethodStereoselective SynthesisPharmacologyEnantioselective SynthesisNatural Product Synthesis
Abstract This review reports on the total synthesis of gabosines, a family of secondary metabolites containing trihydroxylated cyclohexanone or cyclohexenone cores. Analysis of the different stategies used to prepare these natural products and their stereoisomers has been carried out with special attention paid to the methods employed for the formation of the carbocyclic ring. The different methods are compared in a table, and a discussion of future directions of research in this area is presented.
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