Longifolene
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| Names | |
|---|---|
| IUPAC name
(1R,2S,7S,9S)- 3,3,7-trimethyl- 8-methylenetricyclo- [5.4.0.02,9]undecane | |
| Identifiers | |
475-20-7  | |
| 3D model (Jmol) | Interactive image |
| ChEBI | CHEBI:49282  |
| ChemSpider | 1406720 |
| ECHA InfoCard | 100.006.812 |
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| Properties | |
| C15H24 | |
| Molar mass | 204.36 g/mol |
| Density | 0.928 g/cm3 |
| Boiling point | 254 °C (489 °F; 527 K) (706 mm Hg) |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Longifolene is the common (or trivial) chemical name of a naturally occurring, oily liquid hydrocarbon found primarily in the high-boiling fraction of certain pine resins. The name is derived from that of a pine species from which the compound was isolated,[1] Pinus longifolia (obsolete name for Pinus roxburghii Sarg.)[2]
Chemically, longifolene is a tricyclic sesquiterpene. This molecule is chiral, and the enantiomer commonly found in pines and other higher plants exhibits a positive optical rotation of +42.73°. The other enantiomer (optical rotation −42.73°) is found in small amounts in certain fungi and liverworts.
Longifolene is used in organic synthesis for the preparation of dilongifolylborane,[3] a chiral hydroborating agent.
Longifolene is also one of two most abundant aroma constituents of lapsang souchong tea, because the tea is smoked over pine fires.[4]
Total syntheses
Due to the compact tricyclic structure and lack of functional groups, Longifolene is an attractive target for research groups highlighting new synthetic methodologies. Notable syntheses are by Corey,[5][6] McMurray,[7] Johnson,<[8] Oppolzer,[9] and Schultz.[10]
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| Longifolene total synthesis by Corey.svg |
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The Johnson biosynthesis has since been validated as feasible using modern quantum mechanical computational methods. The subsequent cationic cascade mechanism has been shown to go through a non-classical cation intermediate.[11]
Biosynthesis
The biosynthesis of longifolene begins with farnesyl diphosphate (1) (also called farnesyl pyrophosphate) by means of a cationic polycyclization cascade. Loss of the pyrophosphate group and cyclization by the distal alkene gives intermediate 3, which by means of a 1,3-hydride shift gives intermediate 4. After two additional cyclizations, intermediate 6 produces longifolene by a 1,2-alkyl migration.
Use
The borane derivative dilongifolylborane is used in organic synthesis as a chiral hydroborating agent.[12]
External links
References
- ↑ Naffa, P.; Ourisson, G. Bulletin de la Société chimique de France, 1954, 1410.
- ↑ Simonsen, J. L. J. Chem. Soc. 1920, 117, 570.
- ↑ Jadhav, P. K.; Brown, H. C. J. Org. Chem. 1981, 46, 2988.
- ↑ Shan-Shan Yao； Wen-Fei Guo； YI Lu； Yuan-Xun Jiang, "Flavor Characteristics of Lapsang Souchong and Smoked Lapsang Souchong,a Special Chinese Black Tea with Pine Smoking Process", Journal of Agricultural and Food Chemistry, Vol. 53, No.22, (2005)
- ↑ Corey, E. J.; Ohno, Masaji.; Mitra, Rajat B.; Vatakencherry, Paul A. (February 1964). "Total Synthesis of Longifolene". Journal of the American Chemical Society. 86 (3): 478–485. doi:10.1021/ja01057a039.
- ↑ Corey, E. J.; Ohno, Masaji; Vatakencherry, Paul A.; Mitra, Rajat B. (March 1961). "TOTAL SYNTHESIS OF d,l-LONGIFOLENE". Journal of the American Chemical Society. 83 (5): 1251–1253. doi:10.1021/ja01466a056.
- ↑ McMurry, John E.; Isser, Stephen J. (October 1972). "Total synthesis of longifolene". Journal of the American Chemical Society. 94 (20): 7132–7137. doi:10.1021/ja00775a044.
- ↑ Volkmann, Robert A.; Andrews, Glenn C.; Johnson, William S. (August 1975). "Novel synthesis of longifolene". Journal of the American Chemical Society. 97 (16): 4777–4779. doi:10.1021/ja00849a062.
- ↑ Oppolzer, Wolfgang; Godel, Thierry (April 1978). "A new and efficient total synthesis of (.+-.)-longifolene". Journal of the American Chemical Society. 100 (8): 2583–2584. doi:10.1021/ja00476a071.
- ↑ Schultz, Arthur G.; Puig, Salvador (March 1985). "The intramolecular diene-carbene cycloaddition equivalence and an enantioselective Birch reduction-alkylation by the chiral auxiliary approach. Total synthesis of (.+-.)- and (−)-longifolene". The Journal of Organic Chemistry. 50 (6): 915–916. doi:10.1021/jo00206a049.
- ↑ Ho, Gregory J. Org. Chem. 2005, 70, 5139 -5143.
- ↑ Dev, Sukh (1981). "Aspects of longifolene chemistry. An example of another facet of natural products chemistry". Accounts of Chemical Research. 14 (3): 82–88. doi:10.1021/ar00063a004.