Capnellene Synthesis Essay

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  • (−)-Δ9(12)-capnellene

    Names
    Other names

    Capnellene, Δ9(12)-capnellene

    Identifiers

    3D model (JSmol)

    ChemSpider

    PubChemCID

    InChI

    • InChI=1S/C15H24/c1-10-5-6-11-9-15(4)8-7-14(2,3)13(15)12(10)11/h11-13H,1,5-9H2,2-4H3/t11-,12-,13-,15-/m0/s1 N
      Key: YZTNUNFLAAHBMK-ABHRYQDASA-N N
    • InChI=1/C15H24/c1-10-5-6-11-9-15(4)8-7-14(2,3)13(15)12(10)11/h11-13H,1,5-9H2,2-4H3/t11-,12-,13-,15-/m0/s1

      Key: YZTNUNFLAAHBMK-ABHRYQDABA

    SMILES

    • C1(=C)\[C@H]2[C@@H](CC1)C[C@]3([C@@H]2C(C)(C)CC3)C

    Properties

    Chemical formula

    C15H24
    Molar mass204.357 amu

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    N verify (what is YN ?)
    Infobox references

    Capnellene is a naturally occurring hydrocarbon derived from Capnella imbricata, a species of soft coral found in Indonesia. Since the 1970s, capnellene has been targeted for synthesis by numerous investigators due to its stereochemistry, functionality, and the interesting geometry of the carbon skeleton. Many alcohol derivatives of capnellene have demonstrated potential as a chemotherapeutic agent with antibacterial, anti-inflammatory and anti-tumor properties.

    Structure[edit]

    Δ9(12)-capnellene, also referred to simply as capnellene in the literature, is a monounsaturated hydrocarbon of the molecular formula C15H24. It features a tricyclic skeleton, a geminal dimethyl group, a tertiary methyl group, and an exocyclic methylene group.

    Capnellene is also a sesquiterpene, a class of terpenes that are natural semiochemicals. However, it is a non-isoprenoid sesquiterpene, meaning that unlike most sesquiterpenes its structure is not based on a repeated isoprene unit. Capnellene is the presumed biosynthetic precursor to the capnellanols, a group of alcohols based on the capnellene skeleton that are also produced by Capnella imbricata, however the biosynthesis of these compounds has not yet been elucidated.[1][2]

    History[edit]

    The capnellane group became a focal point for synthesis in the 1970s and 80’s. Scientists believed that these compounds had antimicrobial properties, based on an earlier discovery of antimicrobial activity in gorgoniansoft corals[3] and a later study of antimicrobial terpenoid compounds in alcyonarians.[4] It was also postulated that capnellenes also protect the soft coral by preventing larval settlement.[4]

    Capnella imbricata is a rich source of many non-isoprenoid sesquiterpenes, which all share the cis,anti,cis-tricyclo[6.3.0.02,6]undecane ring system.[5] Consequently, the first known isolation of a capnellane derivative was not capnellene but a capnellanol. As part of an ongoing search for terpenoids from marine sources, Kaisin et al. (1974)[6] characterized the most abundant terpenoid, Δ9(12)-capnellene-3β,8β,10α-triol, from colonies of Capnella imbricata. The structure and absolute configuration of the triol were determined by nuclear magnetic resonance (NMR) spectroscopy and later confirmed by x-ray crystallography.[7]

    Kaisin et al. (1974)[6] coined the name “capnellane” for the hydrocarbon skeleton on which the molecule was based. However, Shiekh et al. (1976)[8] also claim to have originated the name. The first isolation of the hydrocarbon form, Δ9(12)-capnellene, was achieved in 1978.[9] Since then, numerous groups have isolated both Δ9(12)-capnellene and its alcohol derivatives.

    Natural Isolation[edit]

    Naturally occurring alcohol derivatives of capnellene have been isolated using simple acetone extraction[10] from Capnella imbricata, a species of soft coral (order Alcyonacea) known as Kenya Tree Coral. Capnella is a widely distributed genus of soft coral, found primarily in the tropical reefs of Indonesia.[11] These corals produce a variety of sterols, sesquiterpenes and diterpenes. Specifically, the capnellanol derivatives found in Capnella serve as a defense system by inhibiting the growth of microorganisms and the settlement of larvae on the coral’s surface.[12] However, the details of this defense mechanism have not been extensively explored. Although the natural synthesis of capnellene and its derivatives is not yet understood, the sesquiterpene hydrocarbon precapnelladiene has been isolated from the same coral and research suggests that may be a biogenetic precursor.[13]

    Total synthesis[edit]

    Capnellene has been a popular target for synthesis due to its molecular architecture, its role in the defense mechanism of soft corals, and the challenge posed by the high degree of functionalization, stereochemical sophistication, and the complexity of the undecane skeleton.[1][2][14] In 1981, the first stereocontrolled synthesis of (±)-Δ9(12)-capnellene was performed in nine steps, with an overall yield of 60%.[5] Their starting reagent was a dimethylated cyclopentenyl carboxaldehyde and the overall synthesis took the form of a series of pentane ring annulations. The second pentane ring was formed by condensation of the aldehyde by vinylmagnesium bromide, followed by Nazarov cyclization of the dienone. A regiospecific [3+2] cyclopentannulation, using ozonolysis and an intramolecular aldol condensation, formed the third ring and a simple dehydration reaction yielded the target capnellene.

    Since the first synthesis, many investigators have successfully assembled capnellene and its derivatives. Approaches to this synthesis are diverse, and include central steps such as annululation, olefin metathesis, radical cyclization, and trapping reactions.[1][2][5][12][15][16] The most heavily cited synthesis in the literature involves two key intermediates formed by a Stille reaction, the palladium-catalyzed coupling of vinyltriflate with vinyl stannane.[17] The readily prepared trimethylcyclopentanone can be converted into vinyl triflate, which is coupled with vinylstannane in the first palladium-catalyzed step to yield the desired divinyl ketone. The second 5-membered ring is formed via Nazarov cyclization, and the product is prepared for a second palladium-catalyzed coupling. This step yields another divinyl ketone, which can be cyclized to an enone, hydrated, and converted to an alkene via olefination to yield capnellene.

    Applications[edit]

    Since the 1960s, marine organisms with robust chemical defense systems have been targeted for “molecular mining,” a method of drug discovery that probes organisms of interest for useful compounds.[18] Chemical agents involved in the defense systems of these organisms often exhibit antibacterial, anti-inflammatory, and chemotherapeutic properties. Capnellene derivatives and their terrestrial counterparts, hirsutanes, demonstrate antibacterial and antitumor properties with pharmacological potential.[1]

    Antitumor Properties[edit]

    Capnellene-8β,10α-diol and its acylated derivatives exhibit significant cytotoxicityin vitro against cervical epitheloid carcinoma (HeLa, oral epidermoid (KB), medulloblastoma (Daoy) and colon adenocarcinoma (WiDr) human tumor cell lines.[19] The diol was also effective against human leukemia, renal leiomyoblastoma, colon and breast cancer cell lines.[20] In the same study, capnellene-8β-ol demonstrated selective toxicity for the renal leiomyoblastoma and ovarian cancer cell lines, while 3β-acetoxycapnellene-8β,10α,14β-triol was active against leukemia cell lines. The antitumor properties of capnellene derivatives have yet to be explored in vivo.

    Anti-Inflammatory Properties[edit]

    Capnellene derivatives have recently been identified as possible treatments for neuropathic pain. Neuropathic pain is characterized by damage to peripheral or central nerves that results in pathological nociceptive transmission, the neuronal process that responds noxious stimuli. Two capnellene derivatives Δ9,12-capnellene-8β,10α-diol and 8α-acetoxy-Δ9,12-capnellene-10α-ol demonstrate potential as analgesics capable of attenuating neuropathic pain. These compounds have been shown in vivo to reduce two proteins that mediate inflammation, cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS).[21]In vivo, Δ9,12-capnellene-8β,10α-diol inhibited hyperalgesia behavior in the mouse model for neuropathic pain in a dose-dependent manner. Additionally, treatment with Δ9,12-capnellene-8β,10α-diol inhibited the up-regulation of immunoreactivity in the mouse model, specifically targeting the production of COX-2.[22] Unlike many non-steroidal anti-inflammatory drugs(NSAIDs), Δ9,12-capnellene-8β,10α-diol is advantageous in its selectivity for the COX isoenzyme COX-2, avoiding many of the gastrointestinal side effects associated with the inhibition of COX-1. This fact would allow for the administration of Δ9,12-capnellene-8β,10α-diol in higher doses, potentially offering significant relief from neuropathic pain.

    References[edit]

    1. ^ abcdStille, John R.; Grubbs, Robert H. (1986). "Synthesis of (.+-.)-.DELTA.9,12-capnellene using titanium reagents". Journal of the American Chemical Society. 108 (4): 855–856. doi:10.1021/ja00264a058. 
    2. ^ abcMehta, Goverdhan.; Murthy, A. Narayana.; Reddy, D. Sivakumar.; Reddy, A. Veera. (1986). "A general approach to linearly fused triquinane natural products. Total syntheses of (.+-.)-hirsutene, (.+-.)-coriolin, and (.+-.)-capnellene". Journal of the American Chemical Society. 108 (12): 3443–3452. doi:10.1021/ja00272a046. 
    3. ^Burkholder, P. R.; Burkholder, L. M. (1958). "Antimicrobial Activity of Horny Corals". Science. 127 (3307): 1174–5. doi:10.1126/science.127.3307.1174. PMID 13555859. 
    4. ^ abCiereszko, LS (March 1962). "Chemistry of coelenterates. III. Occurrence of antimicrobial terpenoid compounds in the zooxanthellae of alcyonarians". Trans N Y Acad Sci. 24 (5 Series II): 502–3. doi:10.1111/j.2164-0947.1962.tb01426.x. PMID 13879507. 
    5. ^ abcPaquette, Leo A.; Stevens, Kenneth E. (1984). "Stereocontrolled total synthesis of the triquinane marine sesquiterpene Δ9(12)-capnellene". Canadian Journal of Chemistry. 62 (11): 2415–2420. doi:10.1139/v84-415. 
    6. ^ abKaisin, M; Sheikh, Y.M.; Durham, L.J.; Djerassi, C.; Tursch, B.; Daloze, D.; Braekman, J.C.; Losman, D.; Karlsson, R. (1974). "Capnellane - a new tricyclic sesquiterpene skeleton from the soft coral ?". Tetrahedron Letters. 15 (26): 2239–2242. doi:10.1016/S0040-4039(01)92222-1. 
    7. ^Karlsson, R. (1977). "The structure and absolute configuration of Δ9(12)-capnellene-3β,8β,10α-triol". Acta Crystallographica Section B. 33 (4): 1143–1147. doi:10.1107/S0567740877005548. 
    8. ^Sheikh, Y; Singy, G.; Kaisin, M.; Eggert, H.; Djerassi, Carl; Tursch, B.; Daloze, D.; Braekman, J.C. (1976). "Terpenoids—LXXI , Chemical studies of marine invertebrates—XIV. Four representatives of a novel sesquiterpene class—the capnellane skeleton". Tetrahedron. 32 (10): 1171–78. doi:10.1016/0040-4020(76)85041-7. 
    9. ^Ayanoglu, E; Gebreyesus, T.; Beechan, C.M.; Djerassi, Carl; Kaisin, M. (1978). "Terpenoids LXXV. Δ9(12)-capnellene, a new sesquiterpene hydrocarbon from the soft coral ? ?". Tetrahedron Letters. 19 (19): 1671–1674. doi:10.1016/S0040-4039(01)94636-2. 
    10. ^Kaisin, M.; Braekman, J.C.; Daloze, D.; Tursch, B. (1985). "Novel acetoxycapnellenes from the alcyonacean capnella imbricata". Tetrahedron. 41 (6): 1067–72. doi:10.1016/S0040-4020(01)96474-9. 
    11. ^"Ocean Coral 'offers pain therapy'". BBC News. 4 August 2009. Retrieved 12 April 2011. 
    12. ^ abLiu, H; Kulkarni, M.G. (1985). "Total synthesis of (±)-Δ9(12)-capnellene". Tetrahedron Letters. 26 (40): 4847–4850. doi:10.1016/S0040-4039(00)94967-0. 
    13. ^Ayanoglu, Eser; Gebreyesus, Tarakegn; Beechan, Curtis M.; Djerassi, Carl (1979). "Terpenoids—LXXVI1Precapnelladiene, a possible biosynthetic precursor of the capnellane skeleton". Tetrahedron. 35 (9): 1035–1039. doi:10.1016/S0040-4020(01)93720-2. 
    14. ^Singh, V; Prathap, S.; Porinchu, M. (1997). "A novel, stereospecific total synthesis of (±)-Δ9(12)-capnellene from p-cresol". Tetrahedron Letters. 38 (16): 2911–2914. doi:10.1016/S0040-4039(97)00501-7. 
    15. ^Curran, D; Chen, Meng-Hsin (1985). "Radical-initiated polyolefinic cyclizations in condensed cyclopentanoid synthesis. Total synthesis of (±)-Δ9(12)-capnellene". Tetrahedron Letters. 26 (41): 4991–4994. doi:10.1016/S0040-4039(01)80834-0. 
    16. ^Little, R. Daniel; Carroll, Gary L.; Petersen, Jeffrey L. (1983). "Total synthesis of the marine natural product .DELTA.9(12)-capnellene. Reversal of regiochemistry in the intramolecular 1,3-diyl trapping reaction". Journal of the American Chemical Society. 105 (4): 928–932. doi:10.1021/ja00342a048. 
    17. ^Crisp, G. T.; Scott, William J.; Stille, John K. (1984). "Palladium-catalyzed carbonylative coupling of vinyl triflates with organostannanes. A total synthesis of (.+-.)-.DELTA.9(12)-capnellene". Journal of the American Chemical Society. 106 (24): 7500–7606. doi:10.1021/ja00336a033. 
    18. ^Livett, Bruce G.; Sandall, David W.; Keays, David; Down, John; Gayler, Ken R.; Satkunanathan, Narmatha; Khalil, Zeinab (December 2006). "Therapeutic applications of conotoxins that target the neuronal nicotinic acetylcholine receptor". Toxicon. 48 (7): 810–29. doi:10.1016/j.toxicon.2006.07.023. PMID 16979678. 
    19. ^Shen, Y.; Tzeng, G.; Kuo, Y.; Taha Khalil, A. (2008). "Cytotoxic Activity of Capnellene-8b,10a-diol Derivatives from a Taiwanese Soft Coral Capnella sp"(PDF). J. Chin. Chem. Soc. 55 (4): 828–833. doi:10.1002/jccs.200800123. Archived from the original(PDF) on 2012-04-02. 
    20. ^Morris, L; Jaspars, Marcel; Adamson, Katy; Woods, Samantha; Wallace, Heather M. (1998). "The capnellenes revisited: New structures and new biological activity". Tetrahedron. 54 (42): 12953–12958. doi:10.1016/S0040-4020(98)00784-4. 
    21. ^Chang, Chin-Hsiang; Wen, Zhi-Hong; Wang, Shang-Kwei; Duh, Chang-Yih (2008). "Capnellenes from the Formosan Soft CoralCapnella imbricata". Journal of Natural Products. 71 (4): 619–21. doi:10.1021/np0706116. PMID 18302334. 
    22. ^Jean, Yen-Hsuan; Chen, Wu-Fu; Sung, Chun-Sung; Duh, Chang-Yih; Huang, Shi-Ying; Lin, Chan-Shing; Tai, Ming-Hon; Tzeng, Shun-Fen; Wen, Zhi-Hong (2009). "Capnellene, a natural marine compound derived from soft coral, attenuates chronic constriction injury-induced neuropathic pain in rats". British Journal of Pharmacology. 158 (3): 713–25. doi:10.1111/j.1476-5381.2009.00323.x. PMC 2765592. PMID 19663884. 

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