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- W2015332557 abstract "Abstract Thirty six different 3-methyl-5-aryl-2,4-pentadienoic acids and esters were synthesized using the Reformatsky and Wittig reactions. The different geometrical isomers were conveniently separated by the dry column technique. Assignment of configuration of the pentadienoic side chain was based on NMR and UV properties. The biological activities of the aromatic analogs of ABA were determined in four bioassays. Most of the analogs were less active than the natural hormone. Only 3-methyl-5- p -chlorophenyl Δ 2 - trans , Δ 4 - trans -pentadienoic acid exhibited high ABA-like activity in all four bioassays." @default.
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- W2015332557 title "Synthesis and biological effects of aromatic analogs of abscisic acid" @default.
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- W2015332557 doi "https://doi.org/10.1016/s0031-9422(00)94349-8" @default.
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