Helvetica Chimica Acta · 1974 · 36 citations · 17 references
Life SciencesBotanyPlant SciencesInsect PhysiologyPlant BiochemistryPlant PhysiologyInsect-plant InteractionsPhenylpropanoid BiosynthesisPlant-insect Chemical InteractionsPlant Defense CompoundsPlant Defense MetabolitesPlant-derived Natural ProductsSaponin Biosynthesis
Abstract The absolute configurations of (+)‐cantharic acid, a chiral derivative of the achiral insect defensive substance cantharidin ( 1 ), and of palasonin, a lower homologue of 1 occurring in the plant Butea frondosa , were shown to be represented by formulas 2 and 3 , respectively ( scheme 1 ). These results were obtained by application of the Horeau method ( table 1 ) on the (+)‐cantharic acid derivatives (+)‐ 5 , (−)‐ 7 , and (−) 11 ( scheme 2 ), and the palasonin derivatives (+)‐ 29 and (+)‐ 30 ( scheme 4 ), as well as by comparison of the chiroptical properties ( tables 2 and 3 ) of a number of derivatives, prepared from either cantharic acid or palasonin. – Attempts to incorporate various radioactively labelled precursors into palasonin ( 3 ), using young and adult plants, have been so far unsuccessful.
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Symmetry rules for optical rotation
John A. Schellman · Accounts of Chemical Research · 1968 · 397 citations
Natural Sciences, Chemistry, Physics +16
E. J. Corey · Journal of the American Chemical Society · 1955 · 131 citations
Some applications of the conformational dissymmetry rule
James H. Brewster · Tetrahedron · 1961 · 120 citations