The ‘citrylidene’ products, obtained when farnesal is condensed with phloroglucinol or malonic acid, by heating in pyridine, are highly stereoselectively dependent on the geometry of the 6-olefin of farnesal; an electrocyclic mechanism is supported.
D. G. Clarke, L. Crombie and D. A. Whiting, J. Chem. Soc., Chem. Commun., 1973, 582 DOI: 10.1039/C39730000582
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