69350-40-9Relevant academic research and scientific papers
Simple methods for the preparation of enantiomerically pure abscisic acid (ABA) analogues from (S)-(+)-ABA
Ward, Dale E.,Gai, Yuanzhu
, p. 2133 - 2142 (1997)
(1'S, 2Z, 4E)-3-Methyl-5-(1-hydroxy-2,6,6-trimethyl-4-oxo-2- cyclohexenyl)-2,4-pentadienoic acid (abscisic acid, ABA) is efficiently converted into the corresponding aldehyde, primary alcohol, and triol derivatives using readily available reagents (oxalyl
