Chemistry:(S)-Ipsdienol
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| Names | |
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| Preferred IUPAC name
(4S)-2-Methyl-6-methylideneocta-2,7-dien-4-ol | |
| Other names
(S)-(+)-Ipsdienol, 2-Methyl-6-methylene-2,7-octadiene-4-ol, Ipsdienol
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C10H16O | |
| Molar mass | 152.237 g·mol−1 |
| Appearance | Colorless |
| Hazards | |
| Flash point | 87 °C (189 °F; 360 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
(S)-Ipsdienol is a terpene alcohol. It is one of the major aggregation pheromones of the bark beetle. It was first identified from Ips confusus, in which it is believed to be a principle sex attractant.[1] It is suggested that the compound plays a role in interspecies communication between Ips latidens and Ips ini, facilitating reductions in competition for breeding material and/or mating interference.[2]
Synthesis
The compound has been synthesized from D-mannitol.[3] Alternative syntheses were realized through the asymmetric isoprenylation of correspondent aldehyde (prenal)[4] and alcohol (prenol).[5] Chiral resolution of racemic precursor has been found[6][7] to provide both enantiomers of ipsdienol in high enantiomeric purity and in preparative scale.
References
- ↑ Silverstein, Robert M.; Rodin, J. Otto; Wood, David L. (October 1966). "Sex Attractants in Frass Produced by Male Ips confusus in Ponderosa Pine". Science 154 (3748): 509–510. doi:10.1126/science.154.3748.509. Bibcode: 1966Sci...154..509S. https://www.science.org/doi/abs/10.1126/science.154.3748.509.
- ↑ Miller, Daniel R.; Borden, John H.; King, G. G. S.; Slessor, Keith N. (1 August 1991). "Ipsenol: an aggregation pheromone for Ips latidens (Leconte) (Coleoptera: Scolytidae)". Journal of Chemical Ecology 17 (8): 1517–1527. doi:10.1007/BF00984685. PMID 24257877.
- ↑ Hanessian, Stephen (1983). Total Synthesis of Natural Products: The 'Chiron' Approach. Pergamon press. pp. 63. ISBN 978-0-08-029247-2.
- ↑ Zhang, Yu-Long; He, Bo-Jun; Xie, Yi-Wen; Wang, Yu-Hao; Wang, Yi-Long; Shen, Yong-Cun; Huang, Yi-Yong (2019). "Enantioselective Isoprenylboration Reaction of Aldehydes Catalyzed by a Chiral Phosphoric Acid". Advanced Synthesis & Catalysis 361 (13): 3074–3079. doi:10.1002/adsc.201900203.
- ↑ Xiang, Ming; Luo, Guoshun; Wang, Yuankai; Krische, Michael J. (2019). "Enantioselective iridium-catalyzed carbonyl isoprenylation via alcohol-mediated hydrogen transfer". Chemical Communications 55 (7): 981–984. doi:10.1039/C8CC09706B. PMID 30608076.
- ↑ Kovalenko, V. N.; Prokhorevich, K. N. (2016). "Improved synthesis of optically active ipsdienol". Russian Journal of Organic Chemistry 52 (5): 757–758. doi:10.1134/S1070428016050250. http://elib.bspu.by/handle/doc/15034.
- ↑ Kovalenko, V. N.; Matyushenkov, E. A. (2012). "Stereoselective synthesis of (R)- and (S)-Ipsdienols, pheromone components of bark beetles of the Ips family". Russian Journal of Organic Chemistry 48 (9): 1168–1172. doi:10.1134/S1070428012090035.
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