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Compound - 10Rme-12Ac [(10R)-10-Methyldodecyl acetate]

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(10R)-10-Methyldodecyl acetate Formula:  C15H30O2  CAS#:  71777-34-9  MW:  242.4  [MS]  [ NMR ]  [Behavioural function]

Dots surface:

Reference(s) for synthesis of (10R)-10-Methyldodecyl acetate [10Rme-12Ac] Chow, S., and Kitching, W. 2002. Hydrolytic kinetic resolution of terminal mono- and bis-epoxides in the synthesis of insect pheromones: routes to (-)-(R)- and (+)-(S)-10-methyldodecyl acetate, (-)-(R)-10-methyl-2-tridecanone, (-)-(R)-(Z)-undec-6-en-2-ol (nostrenol), (-)-(1R,7R )-1,7-dimethylnonyl propanoate. Tetrahedron: Asymmetry. 13:779-794.   Geresh, S., Valiyaveettil, T.J., Lavie, Y., and Shani, A. 1998. Chemoenzymatic synthesis of (R)-(+)-2-methylbutan-1-ol, a chiral synthon for the preparation of optically active pheromones. Tetrahedron: Asymmetry. 9:89-96.   Hjalmarsson, M., and Hoegberg, H.-E. 1985. Synthesis of (R)- and (S)-10-methyl-dodecyl acetate, sex pheromone components of the smaller tea tortrix moth (Adoxophyes sp.), from chiral synthons prepared via asymmetric synthesis. Acta Chem. Scand. B39:793-796.   Sankaranarayanan, S., Sharma, A., Kulkarni, B.A., and Chattopadhyay, S. 1995. Preparation of the versatile chiron, (R)- and (S)-12-(tetrahydropyranyloxy)-3-methyldodecan-1-ol: application to the syntheses of methyl branched insect pheromones. J. Org. Chem. 60:4251-4254.   Tamaki, Y., Sugie, H., Osakabe, M., and Sonnet, P. 1983. Biological activities of R- and S-10-methyldodecyl acetates, the chiral component of the sex pheromone of the smaller tea tortrix moth (Adoxophyes sp.). Appl. Entomol. Zool. 18:292.