Relevant bibliographies by topics / Exo-tricyclo[5.2.1.02

Contents

  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Exo-tricyclo[5.2.1.02'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Exo-tricyclo[5.2.1.02.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

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

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Exo-tricyclo[5.2.1.02"

1

Herberth, Edith. "Hydro- und Carboborierungs-/Oxidationsreaktionen von Tricyclo[4.1.0.02,7]heptan-Derivaten sowie Synthese und Solvolyse-Reaktionen von exo,exo-Bicyclo[1.1.0]butan-2,4-dimethanoldimethansulfonat." Doctoral thesis, 2002. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-4952.

Full text
Abstract:
Die bekannte Umwandlung des Bromtricycloheptans 4 in den Homoallylalkohol 76 durch Hydroborierung/Oxidation wurde anders als früher mit einer in situ aus Natriumborhydrid und elementarem Iod erzeugten Boran-THF-Lösung bewirkt. Darüber hinaus konnten unter den gleichen Bedingungen das Chlortricycloheptan 26 und das Methyltricycloheptan 62 in den Homoallylalkohol 108 bzw. 109 überführt werden. Über 4, 26, 62 und das Phenyltricycloheptan 15 hinaus, dessen Hydroborierung/ Oxidation zum Homoallylalkohol 45a schon früher gelungen war, wurde eine Reihe von Bicyclo[1.1.0]butan-Derivaten mit Boran beha
APA, Harvard, Vancouver, ISO, and other styles
2

Herberth, Edith [Verfasser]. "Hydro- und Carboborierungs-, Oxidationsreaktionen von Tricyclo[4.1.0.02,7]heptan-Derivaten sowie Synthese und Solvolyse-Reaktionen von exo,exo-Bicyclo[1.1.0]butan-2,4-dimethanoldimethansulfonat / vorgelegt von Edith Herberth." 2003. http://d-nb.info/967860105/34.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Exo-tricyclo[5.2.1.02' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography