Publication | Closed Access
Selective Construction of Carbocyclic Eight‐Membered Rings by Ring‐Closing Metathesis of Acyclic Precursors
198
Citations
70
References
2006
Year
Enthalpic FactorsBioorganic ChemistryEngineeringOrganic ChemistryChemistryHeterocycle ChemistrySelective ConstructionMedicinal ChemistryNovel OrganocatalystsBiochemistrySpecific ReagentsNatural Product SynthesisBiomolecular EngineeringHeterocyclicAlkene MetathesisRing-closing MetathesisNatural SciencesAcyclic PrecursorsCarbocyclic Eight‐membered Rings
Although the efficient preparation of cyclooctanoids has remained a long-standing objective, a real breakthrough was possible only relatively recently with the development of more specific reagents and by the development of new reactions. The direct construction of carbocyclic eight-membered rings from acyclic precursors is still a challenge, mainly because of unfavorable entropic and enthalpic factors that preclude ring formation. This Minireview describes the utilization of ring-closing metathesis (RCM) as a new approach to synthesize cyclooctanoids.
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