Liebigs Annalen der Chemie · 1993 · 40 citations · 20 references
Natural SciencesBiochemistryChemistryGreen ChemistryNatural Product BiosynthesisOrganic ChemistryHeterocyclic ChemistryRetrosynthetic AnalysisCarotenoid BiosynthesisCarotenoid ChemistryEnantioselective Synthesis
Abstract Enantiomerically pure ( S )‐2,4,4‐trimethyl‐2‐cyclohexen‐1‐ol ( 1 ) was efficiently converted into four degraded lactonic carotenoids: ( S )‐dihydroactinidiolide ( 5 ), ( S )‐actinidiolide ( 9 ), (6 S ,7a R )‐loliolide ( 11 ) and (6 S ,7a S )‐epiloliolide ( 12 ). ( R )‐Actinidiolide ( 9 ), (6 R ,7a S )‐loliolide ( 11 ) and (6 R ,7a R )‐epiloliolide ( 12 ) were also prepared from ( R )‐ 1 .
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R. Hodges, A. L. Porte · Tetrahedron · 1964 · 92 citations
Sur la composition de l'arôme de thé noir II
J. Bricout, R. Viani, F. Müggler‐Chavan et al. · Helvetica Chimica Acta · 1967 · 67 citations