All the stereoisomers of 7-methylheptadecane (1) and 7,11-dimethylheptadecane (2) were synthesized by starting from the enantiomers of citronellol (3) and methyl 3-hydroxy-2-methylpropanonate (8), respectively. A short synthesis of meso-7,11-dimethylheptadecane [(7R,11S)-2] was achieved starting from meso-2,6-dimethylheptanedioic acid [(2R,6S)-21]. A mixture of (S)-1 and (7R,11S)-2 is the pheromone of the spring hemlock looper moth (Lambdina athasaria) and the pitch pine looper moth (L. pellucidaria).
No takes yet. Share an insight, caveat, or question.
Shirai et al. (1999) studied this question.
Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context: