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Veticadinol Knoevenagel reaction

In his synthesis of the cadinane-sesquiterpene veticadinol (69), Lutz Tietze employed a sequence of Knoevenagel condensation of (i )-citronellal (66) and dimethylmalonate followed by an ene reaction provide 68 with the requisite trans stereochemistry in what was to become the decalin core of veticadinol 69. ... [Pg.489]


See also in sourсe #XX -- [ Pg.373 ]

See also in sourсe #XX -- [ Pg.373 ]

See also in sourсe #XX -- [ Pg.373 ]




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Knoevenagel reaction

Veticadinol

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