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Journal articles on the topic 'Exo-tricyclo[5.2.1.02'

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Published: 5 June 2025

Last updated: 2 August 2025

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1

Bosman, W. P., J. M. M. Smits, Paul T. Beurskens, P. P. M. A. Dols, and A. J. H. Klunder. "Crystal and molecular structure ofexo,exo-8,9-diiodo-5-methyl-exo-tricyclo [5.2.1.02, 6]dec-4-en-3-one, C11H12I2O." Journal of Crystallographic and Spectroscopic Research 23, no. 12 (1993): 1025–27. http://dx.doi.org/10.1007/bf01185556.

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2

Vasilkevich, Oleksandr, Yurii Klimko та Svyatoslav Levandovskii. "SYNTHESIS AND BIOLOGICAL ACTIVITY OF SOME 2-SUBSTITUTED DERIVATIVES OF TRICYCLO [5.2.1.02,6]DEСAN". Deutsche internationale Zeitschrift für zeitgenössische Wissenschaft 84 (16 липня 2024): 15–18. https://doi.org/10.5281/zenodo.12752511.

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Based on individual exo- and endo-isomers of tricyclo[5.2.1.02.6]deca-2-carboxylic acid, various nitrogencontaining derivatives were synthesized: amides, thioamides, amines, alkylamines, amidines. Antiviral properties tested.

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3

Childs, Ronald F., Barry M. Duffey, and Mailvaganam Mahendran. "Photoisomerization of the AlEtCl2 complex of endo-tricyclo[5.2.1.02,6]deca-4,8-dien-3-one." Canadian Journal of Chemistry 64, no. 6 (1986): 1220–23. http://dx.doi.org/10.1139/v86-202.

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Irradiation of the AlEtCl2 complex of endo-tricyclo[5.2.1.02,6]deca-4,8-dien-3-one (1AL) yielded the AlEtCl2 complex of exo-tricyclo[5.3.0.02,6]deca-4,8-dien-3-one (3AL). The structure of 3, which was obtained on treatment of the irradiated solution with water, was established by its reduction to give the known exo-tricyclo[5.3.0.02,6]decan-3-one. The photoisomerization of 1AL could not be driven to completion as 3AL underwent a photoisomerization to regenerate 1AL. Control experiments showed that the interconversions of 1AL and 3AL were photochemically and not thermally induced. Irradiation o

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4

Ragauskas, Arthur J., and J. B. Stothers. "13C magnetic resonance studies. 120. The Simmons–Smith reaction with some silyl enol ethers. Unusual ring expansions of some norcamphorsti." Canadian Journal of Chemistry 63, no. 11 (1985): 2969–74. http://dx.doi.org/10.1139/v85-492.

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Unexpected difficulties with Simmons–Smith cyclopropanation of the trimethylsilyl enol ether of exo-tricyclo[3.2.1.02,4]-octan-6-one led to a reexamination of this reaction with the parent norcamphor derivative which under "concentrated" conditions gave ring-expanded allylic ethers in low yield. With the tert-butyldimethylsilyl ethers, however, the allylic product is formed in high yield in the norcamphor and exo-trimethylenenorcamphor (tricyclo[5.2.1.02,6]decan-8-one) systems. The tert-butyldimethylsilyl enol ethers of bicyclo[3.2.1]octan-6-one and nopinone do not undergo ring expansion under

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5

Kazakov, A. I., L. S. Yanovskiy, Yu V. Tomilov, et al. "Thermal Decomposition of Synthetic Cage Hydrocarbons and Their Mixtures." Нефтехимия 63, no. 2 (2023): 268–76. http://dx.doi.org/10.31857/s0028242123020119.

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The kinetics of thermal decomposition of cage hydrocarbons, specifically exo-tricyclo[5.2.1.02.6]decane (exo-TCD) and exo,endo-tetracyclo[5.3.1.02,6.08,10]undecane (TCU-1, a monocyclopropanated analog of exo-TCD), as well as their mixture (1 : 3 w/w) has been investigated. These compounds were compared in terms of thermal stability. The molar concentrations of the resultant gaseous products were determined experimentally. The equilibrium composition of the decomposition products was quantified, and the thermal effects of the thermal decomposition under thermodynamic and kinetic reaction contr

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6

Clements, Michael T. M., Ross E. Klinck, Sriyawathie Peiris, Arthur J. Ragauskas та J. B. Stothers. "13C magnetic resonance studies 133. An examination of the effect of conformation on β-enolization in some bicyclo[3.2.1]octan-2-ones". Canadian Journal of Chemistry 66, № 3 (1988): 454–60. http://dx.doi.org/10.1139/v88-079.

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To assess the influence of the conformation of the cyclohexanone moiety in bicyclo[3.2.1]octan-2-ones on the reactivity for β-enolate rearrangement, the behavior of three derivatives under typical homoenolization conditions has been examined for comparison with 3,3-dimethylbicyclo[3.2.1]octan-2-one (1), which was known to be smoothly converted to the [3.3.0] isomer 2. For this purpose, endo-3-tert-butyl-exo-3-methylbicyclo[3.2.1]octan-2-one (8), endo-9-tert-butyl-exo-9-methyl-exo-tricyclo[5.3.1.02,6]undecan-8-one (9), and 9,9-dimethyl-endo-tricyclo[5.3.1.02,6]undecan-8-one (10) were prepared a

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7

Haufe, G�nter, Ren� Faure, and Henri Loiseleur. "Crystal and molecular structure ofanti,exo,exo-5,10,12-tribromo-13-oxa-exo-tricyclo [7.3.1.02,6] tridecane." Journal of Crystallographic and Spectroscopic Research 17, no. 5 (1987): 653–59. http://dx.doi.org/10.1007/bf01167122.

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8

Koshchii, I., O. Vasilkevich, and Yu. Klimko. "BECKMAN REACTION OF KETOXIMES OF THE TRICYCLO[5.2.1.02,6]DECAN SERIES WITH THIONYL CHLORIDE." Sciences of Europe, no. 145 (July 26, 2024): 15–20. https://doi.org/10.5281/zenodo.12909376.

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As a result of the Beckmann reaction, the oximes tricyclo[5.2.1.02,6]decan-9-one, tricyclo[5.2.1.02,6]dec-3-en-9-one and tricyclo[5.2.1.02,6]dec-4-ene -9-one with thionyl chloride forms transmutation products - lactams and fragmentation products - unsaturated nitriles and isomeric chloronitriles.

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9

Liaw, Der-Jang, Been-Yang Liaw, and En-Tang Kang. "Synthesis and characterization of new cardo polyamide-imides containing ether and tricyclo[5.2.1.02, 6]decane groups." Macromolecular Chemistry and Physics 200, no. 10 (1999): 2402–6. http://dx.doi.org/10.1002/(sici)1521-3935(19991001)200:10<2402::aid-macp2402>3.0.co;2-c.

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10

Burritt, Andrew, James M. Coxon, Peter J. Steel, and Barry I. Whittington. "Bromination of exo- and endo-Tricyclo[3.2.1.02,4]octane." Journal of Organic Chemistry 60, no. 9 (1995): 2812–19. http://dx.doi.org/10.1021/jo00114a034.

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11

Koval'skaya, S. S., and N. G. Kozlov. "ChemInform Abstract: Mannich Condensation of exo-2,exo-6-Tricyclo[5.2.1.02.6]decan-8-one." ChemInform 33, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200250127.

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12

Ekeland, R. A., and P. W. Jennings. "Reaction of exo-tricyclo[3.2.1.02,4]-6-Octanone with Zeise's dimer." Journal of Organometallic Chemistry 281, no. 2-3 (1985): 397–402. http://dx.doi.org/10.1016/0022-328x(85)87125-4.

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13

Coxon, James M., Peter J. Steel, Andrew Burritt, and Barry I. Whittington. "Bromination of exo- and endo-tricyclo[3.2.1.02,4]oct-6-ene." Tetrahedron 51, no. 29 (1995): 8057–72. http://dx.doi.org/10.1016/0040-4020(95)00420-d.

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14

BURRITT, A., J. M. COXON, and P. J. STEEL. "ChemInform Abstract: Bromination of exo-Tricyclo(3.2.2.02,4)non-6-ene." ChemInform 27, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199645113.

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15

Peiris, Sriyawathie, J. B. Stothers та Shirley E. Thomas. "13C magnetic resonance studies. 138. An examination of the [3.2.2.0] → [4.2.1.0] rearrangement via β-enolization and H/D exchange in tricyclic ketones". Canadian Journal of Chemistry 67, № 2 (1989): 187–92. http://dx.doi.org/10.1139/v89-031.

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The behavior of the endo and exo isomers of 7,7-dimethyltricyclo[3.2.2.02,4]nonan-6-one (9, 17) under strongly basic conditions (t-BuO−/t-BuOH/185 °C) has been examined. In both cases rearrangement to the corresponding 8,8-dimethyl-tricyclo[4.2.1.02,4]nonan-7-one (11, 18) was found, with the exo isomer reacting approximately 8 times faster. Experiments in tert-butyl alcohol-O-d1 were carried out to determine the specific sites, the relative rates, and the stereochemistry of deuterium incorporation in the initial ketones. Although H/D exchange occurs most readily at the cyclopropyl methylene ca

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16

Bailey, William F., and Justin D. Fair. "Intramolecular carbolithiation cascades as a route to a highly strained carbocyclic framework: competition between 5-exo-trig ring closure and proton transfer." Beilstein Journal of Organic Chemistry 9 (March 14, 2013): 537–43. http://dx.doi.org/10.3762/bjoc.9.59.

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The preparation of fairly strained carbocyclic ring systems by intramolecular 5-exo-trig ring closure has been well documented, and the absence of proton transfers that would compromise such cyclizations is a hallmark of this chemistry. In an effort to explore the limitations of this approach to more highly strained systems, the preparation of a stellane (tricyclo[3.3.0.03,7]octane) framework by an intramolecular carbolithiation cascade involving three coupled 5-exo-trig cyclizations of the vinyllithium derived from 2-bromo-4-vinyl-1,6-heptadiene by lithium–bromine exchange was investigated. T

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17

Burritt, Andrew, James M. Coxon, and Robert G.A.R. Maclagan. "Studies of proton addition to exo and endo-tricyclo[3.2.1.02,4]octane." Tetrahedron 51, no. 42 (1995): 11557–72. http://dx.doi.org/10.1016/0040-4020(95)00717-m.

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18

Hertkorn, N., and F. H. Köhler. "Selektive Metallierung von BicycIo[3.2.1]octa-2,6-dien, II Distannylierte Derivate und stannylierte tricyclische Sekundärprodukte / Selective Metalation of Bicyclo[3.2.1]octa-2,6-diene, II Distannylated Derivatives and Stannylated Tricyclic Secondary Products." Zeitschrift für Naturforschung B 43, no. 11 (1988): 1405–15. http://dx.doi.org/10.1515/znb-1988-1105.

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Abstract Distannylated bicyclo[3.2.1]octa-2,6-diene (1) with (CH3)3 Sn groups in positions exo-4 and 7 (7a), endo-4 and 7 (7b), exo-4 and 6 (7c), and probably exo-4 and endo-4 (7d) are obtained when 1 is treated first with an excess of n-BuLi/t-BuOK in alkane and then with (CH3)3 SnCl. Byproducts are monostannylated derivatives of 1 and l,4-bis(trimethylstannyl)but-2-ene (3). The formation of 7a/b/c is best understood when the two possible bicyclo[3.2.1]octa-2,6-dienyl dianions are generated as intermediates. 3,exo-4-Bis(trimethylstannyl)bicyclo[3.2.1]octa-2,6-diene (7e) is ob-tained from the

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19

COXON, J. M., P. J. STEEL, A. BURRITT, and B. I. WHITTINGTON. "ChemInform Abstract: Bromination of exo- and endo-Tricyclo(3.2.1.02,4)oct-6-ene." ChemInform 26, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199545074.

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20

Abdul Ajees, A., N. Palani, and K. K. Balasubramanian. "2-(exo-Tricyclo[5.2.1.02,6]deca-4,8-dien-3-endo-yl)acetaldehyde 2,4-dinitrophenylhydrazone." Acta Crystallographica Section C Crystal Structure Communications 58, no. 7 (2002): o433—o435. http://dx.doi.org/10.1107/s010827010200968x.

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21

MacWhorter, Susan E., and Neil E. Schore. "Stereocontrolled synthesis of functionalized diquinanes from Pauson-Khand-derived exo-tricyclo[5.2.1.02,6]decenones." Journal of Organic Chemistry 56, no. 1 (1991): 338–46. http://dx.doi.org/10.1021/jo00001a063.

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22

BURRITT, A., J. M. COXON, and R. G. A. R. MACLAGAN. "ChemInform Abstract: Studies of Proton Addition to exo- and endo-Tricyclo(3.2.1.02,4)octane." ChemInform 27, no. 9 (2010): no. http://dx.doi.org/10.1002/chin.199609073.

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23

Hellou, Jocelyne, Gervais Bérubé, Michael J. Newlands, Alex G. Fallis, and Eric J. Gabe. "Intramolecular Diels–Alder reactions of cyclopentadiene systems: Model studies for the total synthesis of the capnellenes." Canadian Journal of Chemistry 66, no. 3 (1988): 439–48. http://dx.doi.org/10.1139/v88-077.

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Model studies for a general intramolecular Diels–Alder approach to the tricyclo[6.3.0.02,6]undecene skeleton common to the capnellene marine sesquiterpenes are described. Suitably functionalized cyclopentadiene systems 14 and 21 were synthesized and their cycloaddition reactivity examined. Triene 14 cyclized to the tricyclic adducts 15 and 16. In contrast, the anticipated product 22 from intramolecular cycloaddition of triene 21 was not formed in isolatable yield. Instead the minor adduct (10% yield) possessed an exocyclic double bond and was assigned structure 30 based on its relative stabili

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24

Bobylyova, Alia A., Andrey V. Khoroshutin, Elena V. Lukovskaya, Tõnis Pehk, and Nina A. Belikova. "Addition of dibromocarbene to tricyclo[4.3.0.03,7]nona-4,8-diene (brexadiene). Synthesis of exo-4,5,10,exo-11-tetrabromotricyclo[5.4.0.03,8]undeca-5,9-diene." Mendeleev Communications 6, no. 3 (1996): 112–13. http://dx.doi.org/10.1070/mc1996v006n03abeh000604.

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25

Coxon, James M., Peter J. Steel, Barry I. Whittington, and Merle A. Battiste. "Corner attack on exo- and endo-tricyclo[3.2.1.02,4]octane by deuteron and mercuric ions." Journal of Organic Chemistry 54, no. 6 (1989): 1383–91. http://dx.doi.org/10.1021/jo00267a029.

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26

Moers, F. G., J. M. M. Smits, P. T. Beurskens, J. Zhu, and A. J. H. Klunder. "endo-5-Methyl-exo-6-phenylseleno-endo-tricyclo[5.2.1.02,6]dec-8-en-3-one." Acta Crystallographica Section C Crystal Structure Communications 51, no. 11 (1995): 2335–38. http://dx.doi.org/10.1107/s0108270195006251.

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27

MACWHORTER, S. E., and N. E. SCHORE. "ChemInform Abstract: Stereocontrolled Synthesis of Functionalized Diquinanes from Pauson- Khand-Derived exo-Tricyclo(5.2.1.02,6)decenones." ChemInform 22, no. 20 (2010): no. http://dx.doi.org/10.1002/chin.199120138.

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28

DOLS, P. P. M. A., A. J. H. KLUNDER, and B. ZWANENBURG. "ChemInform Abstract: Halogen Addition to endo- and exo-Tricyclo(5.2.1.02,6)deca-4,8-dien-3- ones." ChemInform 25, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199412146.

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29

Srikrishna, Adusumilli, and G. Veera Raghava Sharma. "Synthesis of chiral tricyclo[3.2.1.02,7]octanes by an efficient 3-exo-trig radical cyclisation reaction 1." Journal of the Chemical Society, Perkin Transactions 1, no. 2 (1997): 177–82. http://dx.doi.org/10.1039/a601315e.

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30

Hudzik, Jason M., Álvaro Castillo, and Joseph W. Bozzelli. "Bond Energies and Thermochemical Properties of Ring-Opened Diradicals and Carbenes of exo-Tricyclo[5.2.1.02,6]decane." Journal of Physical Chemistry A 119, no. 38 (2015): 9857–78. http://dx.doi.org/10.1021/acs.jpca.5b05564.

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31

Dols, Paul P. M. A., Antonius J. H. Klunder, and Binne Zwanenburg. "A two-step chirality transfer from (−)-endo- to (−)-exo-tricyclo[5.2.1.026]deca-4,8-dien-3-one." Tetrahedron Letters 34, no. 19 (1993): 3181–84. http://dx.doi.org/10.1016/s0040-4039(00)93412-9.

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32

MOERS, F. G., J. M. M. SMITS, P. T. BEURSKENS, J. ZHU, and A. J. H. KLUNDER. "ChemInform Abstract: endo-5-Methyl-exo-6-phenylseleno-endo-tricyclo(5.2.1.02,6)dec-8-en-3- one." ChemInform 27, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199613024.

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33

SATO, M., H. HATTORI, M. MURAKAMI, and C. KANEKO. "ChemInform Abstract: An Improved Synthetic Method for Both Enantiomers of Tricyclo(5.2.1.02, 6)deca-4,8-dien-3-one by Means of Chemoenzymatic Dissymmetrization of a meso-Compound." ChemInform 25, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199419102.

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34

BOBYLYOVA, A. A., A. V. KHOROSHUTIN, E. V. LUKOVSKAYA, T. PEHK, and N. A. BELIKOVA. "ChemInform Abstract: Addition of Dibromocarbene to Tricyclo(4.3.0.03,7)nona-4,8-diene ( Brexadiene). Synthesis of exo-4,5,10,exo-11-Tetrabromotricyclo(5.4.0. 03,8)undeca-5,9-diene (III)." ChemInform 27, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199638116.

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35

Jenan, Mohammed Ubaid, Jawad Kadhim Mohanad, and Hadi Hameed Imad. "Study of Bioactive Methanolic Extract of Camponotus fellah Using Gas Chromatography – Mass Spectrum." International Journal of Toxicological and Pharmacological Research 8, no. 6 (2017): 434–39. https://doi.org/10.5281/zenodo.12770188.

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GC-MS analysis of <em>Camponotus fellah</em> revealed the existence of the  Cyclopentaneacetaldehyde ,2-formyl-3-methyl-α-methylene-, Cyclohexene, 1-methyl-5-(1-methylethenyl)-,(R)-, Bicyclo[5.1.0]octane, 8-methylene-,5-Methyl-6-phenyltetrahydro – 1,3-oxazine-2-thione, Decane, 1-Heptanol, 2-propyl, Octane, -4-methyl, Cyclopentanol, 2-(2-propynyloxy)-, trans-, Hydroxylamine, O-decyl, Trans-2-Ethyl-2-hexen-1-ol, Cyclopropene,1-methyl-3-(2-methylcyclopropyl)-, 10-methyl-endo-tricyclo[5.2.1.0(2.6)]decane, Undecen-1-yne, (Z, Exo-Norbornyl propionate, 5,8,10-Undecatrien-3-

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36

Liu, Qi Mei, Dang Quan Zhang, Kuan Peng та Wan Xi Peng. "Deep Analysis on Bioindustry Prospects of 40°С Volatiles of Cinnamomum camphora Branches". Key Engineering Materials 480-481 (червень 2011): 266–71. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.266.

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Cinnamomum camphora has been used to heal some specific diseases in the Chinese Folk for a long time. In order to explore the wide utilization in biomedicine and spicery, the chemical components of helium volatiles from the fresh branches of C. camphora were studied by TD-GC/MS. The analytical result by TD-GC/MS showed that 50 peaks were obtained from the helium volatiles from the fresh branches of C. camphora and 46 chemical compounds representing 99.993% of the total areas were identified. The results showed that the main components were as: Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)

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37

Li, Dan, Xiaori Sun, Limin Li, Suqing Wang, Lintong Wang, and Xuefeng Liu. "Vapor pressures and volumetric properties for binary mixtures of propylene glycol monomethyl ether and exo-tricyclo[5.2.1.02.6]decane." Journal of the Taiwan Institute of Chemical Engineers 45, no. 3 (2014): 823–27. http://dx.doi.org/10.1016/j.jtice.2013.09.003.

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38

Abbasoglu, Rza. "DFT and MP2 study on the electrophilic addition reaction of bromine to exo-tricyclo[3.2.1.02.4]oct-6-ene." Journal of Molecular Modeling 16, no. 4 (2009): 781–88. http://dx.doi.org/10.1007/s00894-009-0608-9.

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39

DOLS, P. P. M. A., A. J. H. KLUNDER, and B. ZWANENBURG. "ChemInform Abstract: A Two-Step Chirality Transfer from (-)-endo- to (-)-exo-Tricyclo(5.2.1. 02,6)deca-4,8-dien-3-one." ChemInform 24, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199340163.

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40

DOLS, P. P. M. A., M. M. H. VERSTAPPEN, A. J. H. KLUNDER, and B. ZWANENBURG. "ChemInform Abstract: Regio- and Stereoselectivity of Additions of Organometallics to endoand exo-Tricyclo(5.2.1.02,6)deca-4,8-dien-3-ones." ChemInform 25, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199412145.

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41

Li, Qing, Dang Quan Zhang, Qi Mei Liu та Kuan Peng. "Determination of Bioactive Components of 60°С Volatiles from Cinnamomum camphora Branches by TD-GC/MS". Advanced Materials Research 230-232 (травень 2011): 852–56. http://dx.doi.org/10.4028/www.scientific.net/amr.230-232.852.

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The chemical components of helium volatiles from the fresh branches of Cinnamomum camphora were studied by TD-GC/MS. The analytical result by 60°С-based TD-GC/MS showed that 55 peaks were obtained from the helium volatiles from the fresh branches of Cinnamomum camphora and 53 chemical compounds were identified. The results showed that the main components were as: Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)- (15.4328%), 1,3-Benzodioxole, 5-(2-propenyl)- (14.881%), Tricyclo[2.2.1.0(2,6)]heptane, 1,7-dimethyl-7-(4-methyl-3-pentenyl)-, (-)- (12.694%), p-menth-1-en-8-ol (9.832%), Bicyclo[2.2

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42

THURING, J. W. J. F., G. H. L. NEFKENS, M. A. WEGMAN, A. J. H. KLUNDER, and B. ZWANENBURG. "ChemInform Abstract: Enzymatic Kinetic Resolution of 5-Hydroxy-4-oxa-endo-tricyclo(5.2.1.02, 6)dec-8-en-3-ones: A Useful Approach to D-Ring Synthons for Strigol Analogues with Remarkable Stereoselectivity." ChemInform 28, no. 9 (2010): no. http://dx.doi.org/10.1002/chin.199709037.

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Гасанов, А. Г. о., И. Г. о. Аюбов, С. С. о. Алиев, М. М. г. Гурбанова та Ч. К. г. Салманова. "ИЗУЧЕНИЕ РЕАКЦИИ КАТАЛИТИЧЕСКОГО ГИДРИРОВАНИЯ ДИЦИКЛОПЕНТАДИЕНА". Вестник КНИИ РАН. Серия Естественные и технические науки, № 2(21) (17 липня 2025): 102–15. https://doi.org/10.69537/vkniiran.2025.21.2.009.

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Гидрирование дициклопентадиена (трицикло[5.2.1.02,6]-дека-3,8-диена) в при-сутствии гомо- и гетерогенных катализаторов является одной из ключевых реакций нефтехимиче-ского синтеза, приводящая к образованию смеси эндо- и экзо-изомеров тетрагидродициклопента-диена, являющегося основным компонентом реактивных топлив. В этой связи актуальность этой реакции не ослабевает и по сегодняшний день, а количество работ в направлении поиска новых оптимальных катализаторов для этой реакции, а также усовершенствования оптимальных режим-ных параметров процесса ежегодно возрастает. В представленной работе нами

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Suri, Suresh Chander, Angelica C. Cabrera, Edward J. Wucherer, and Stephen L. Rodgers. "Synthesis and Structure Elucidation of 8-Methyl- and 9-Methyl-exo-2-carbomethoxy-endo-tricyclo[5.2.1.02,6]deca-3,8-dien-5-ones." Synthetic Communications 27, no. 5 (1997): 841–51. http://dx.doi.org/10.1080/00397919708004205.

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Liu, Qi Mei, та Wan Xi Peng. "80°С-Based TD-GC/MS Analysis of Chemical Components from Branches of Cinnamomum camphora". Key Engineering Materials 480-481 (червень 2011): 466–71. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.466.

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The analytical result by 80°С-based TD-GC/MS showed that 65 peaks were obtained from the helium volatiles from the fresh branches of Cinnamomum camphora and 60 chemical compounds were identified. The results showed that the main components were as: 1,3-Benzodioxole, 5-(2-propenyl)- (12.629%), Tricyclo[2.2.1.0(2,6)]heptane, 1,7-dimethyl-7-(4-methyl-3-pentenyl)-, (-)- (10.302%), 3-Cyclohexene-1-methanol, .alpha.,.alpha.4-trimethyl- (9.084%), Bicyclo[2.2.1] heptan-2-one, 1,7,7-trimethyl-, (1R)- (7.406%), Nerolidol (6.695%), Bicyclo[2.2.1]heptane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)-, (1S

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Moers, F. G., H. Behm, Paul T. Beurskens, et al. "Crystal and molecular structure of ethyl-endo-5-acetoxy-exo-3,4-epoxy-4-endo-tricyclo[5.2.1.02,6]deca-8-ene-2-carboxylate, C15H18O5." Journal of Crystallographic and Spectroscopic Research 21, no. 2 (1991): 217–21. http://dx.doi.org/10.1007/bf01161068.

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Coxon, James M., Peter J. Steel, and Barry I. Whittington. "Corner attack on endo- and exo-tricyclo[3.2.1.02,4]oct-6-ene by deuterium and mercuric ions: the effect of electrophile on reaction course." Journal of Organic Chemistry 54, no. 15 (1989): 3702–9. http://dx.doi.org/10.1021/jo00276a036.

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SURI, S. C., A. C. CABRERA, E. J. WUCHERER, and S. L. RODGERS. "ChemInform Abstract: Synthesis and Structure Elucidation of 8-Methyl- and 9-Methyl-exo-2- carbomethoxy-endo-tricyclo(5.2.1.02,6)deca-3,8-dien-5-ones." ChemInform 28, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199726107.

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SRIKRISHNA, A., and G. V. R. SHARMA. "ChemInform Abstract: Chiral Synthons from Carvone. Part 23. Synthesis of Chiral Tricyclo(3. 2.1.02,7)octanes by an Efficient 3-exo-trig Radical Cyclization Reaction." ChemInform 28, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199722082.

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Kirchen, Roger P., Ted S. Sorensen, and Steven M. Whitworth. "A mechanistic study of the carbocation route from tetrahydrodicyclopentadiene to the adamantane ring." Canadian Journal of Chemistry 71, no. 12 (1993): 2016–27. http://dx.doi.org/10.1139/v93-251.

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The energy profile for the transformation of the endo-tetrahydrodicyclopentadienyl cation A into the 1-adamantyl cation R has been probed by means of six separate experiments employing superacid techniques. Of the approximately 14 cations between A and R, required as intermediates for the above transformation, it can be shown that only one of these is capable of direct observation. This cation, the tricyclo[5.2.1.03.8]dec-3-yl (homobrendyl) cation J, is characterized in detail in one of the six experiments. The rate of the rearrangement of J into the 1-adamantyl cation has been measured. Catio

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