Title: | "Synthesis of the four stereoisomers of 2,6-dimethyloctane-1,8-dioic acid, a component of the copulation release pheromone of the cowpea weevil, Callosobruchus maculatus" |
Author(s): | Nakai T; Yajima A; Akasaka K; Kaihoku T; Ohtaki M; Nukada T; Ohrui H; Yabuta G; |
Address: | "Department of Fermentation Science, Faculty of Applied Biological Science, Tokyo University of Agriculture, Japan" |
Journal Title: | Biosci Biotechnol Biochem |
ISSN/ISBN: | 0916-8451 (Print) 0916-8451 (Linking) |
Abstract: | "A diastereomeric mixture and the four stereoisomers of 2,6-dimethyloctane-1,8-dioic acid (2), a copulation release pheromone of the cowpea weevil, Callosobruchus maculatus, were synthesized. The stereoisomeric purities of the four synthetic isomers of 2 were determined by the HPLC analyses of their bis-2-(2,3-anthracenedicarboximide)-1-cyclohexyl esters" |
Keywords: | "Acyclic Monoterpenes Chromatography, High Pressure Liquid Dicarboxylic Acids/*chemical synthesis/chemistry Indicators and Reagents Magnetic Resonance Spectroscopy Molecular Conformation Oxidation-Reduction Sex Attractants/*chemical synthesis/chemistry Spe;" |
Notes: | "MedlineNakai, Tomonori Yajima, Arata Akasaka, Kazuaki Kaihoku, Takayuki Ohtaki, Miki Nukada, Tomoo Ohrui, Hiroshi Yabuta, Goro eng England 2005/12/27 Biosci Biotechnol Biochem. 2005 Dec; 69(12):2401-8. doi: 10.1271/bbb.69.2401" |