Method for isolating insect sex pheromones

Chemistry of carbon compounds – Miscellaneous organic carbon compounds – C-metal

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260419, 260601R, 260593P, 260594, 2604659, 260652P, 260561R, 260561P, 260561S, 260561N, 260561B, 260555C, 260552R, 260583E, 260583EE, 260583F, 260583H, 260583N, 260584R, 260609C, 260609B, 560147, 560155, 560218, 562554, 562580, 562555, 568917, 568693, C09F 510, C11B 300, C07C 6900, C07C 9716, C07C 8300

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041706013

ABSTRACT:
The isomers of synthetic insect sex pheromones or their precursors are separated by selectively forming an inclusion complex with the E-isomer and urea or thiourea. In order for the E-isomer complex to form selectively it is necessry that the mono-olefin which forms the complex have a primary, linear chain of at least 7 atoms, a molecular diameter of 2.8-6A, and a polar functional group having transverse dimensions of less than 6A. Branching between the olefinic bond and the polar functional group is limited to methyl groups.

REFERENCES:
butenandt, A., et al., Liebigs Ann. Chem. 658 39(1962).
Schlenk et al., J. Am. Chem. Soc., vol. 72, pp. 5001-5004 (1950).
Chemical Abstracts, vol 65:4213y.
Chemical Abstracts, vol. 72:33516n.
Chemical Abstracts, vol. 61:2053g.
Swern, D. et al., J. Am. Chem. Soc., 74, pp. 655-657 (1952).

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