Journal of the Chemical Society Chemical Communications · 1979 · 19 citations · 0 references
Natural SciencesBiochemistryChemistryOrganic ChemistryHeterocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisTerpenoid BiosynthesisCarbon-carbon Bond FormationNatural Product SynthesisRing-forming Reactions
Acid catalysed cyclisation of the olefinic β-hydroxy selenide (5) afforded the cyclic compound (7) which was converted into safranal (16)via the olefinic alcohol (12), diolefinic alcohol (14), and aldehyde (15).