Organic Letters · 2010 · 30 citations · 53 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryOrganometallic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisRetrosynthetic AnalysisRing-closing MetathesisRing-forming Reactions
A general route to linear triquinanes including a formal synthesis of (+/-)-Delta(9(12))-capnellene is described. This cascade strategy combines an intramolecular Diels-Alder reaction tandem metathesis protocol to generate the linear cis-anti-cis-tricyclo[6.3.0.0(2,6)]undecane skeleton directly. Significantly, the ring-closing-ring-opening-cross-metathesis (RCM-ROM-CM) sequence with our norbornene adducts is the only observed mechanism.
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