Academic literature on the topic 'Polycyclic cage compounds'

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Journal articles on the topic "Polycyclic cage compounds"

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Bauer, Ingmar, and Wolf D. Habicher. "In,out-Isomerism of Phosphorus Bridgehead Cage Compounds. A Review." Collection of Czechoslovak Chemical Communications 69, no. 6 (2004): 1195–230. http://dx.doi.org/10.1135/cccc20041195.

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The chemistry and stereochemical peculiarities, especially the phenomenon of in,out-isomerism of bi- and polycyclic compounds with one or more phosphorus bridgehead atoms, are reviewed in the present paper. The appearance of in,out-isomers depends on the ring size of the bi- and polycycles. In general graphic in,out-isomerism becomes only possible in medium sized ring systems and in particular in macrocyclic compounds. However even bicyclic systems containing small rings can be trans-configured if the third chain is long and flexible enough hence giving rise to pseudo-in,out-isomerism. In-phos
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Masusai, Chonticha, Darunee Soorukram, Chutima Kuhakarn, et al. "Synthesis of gem-Difluoromethylenated Polycyclic Cage Compounds." Journal of Organic Chemistry 80, no. 3 (2015): 1577–92. http://dx.doi.org/10.1021/jo502501v.

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James, Beena, Nigam P. Rath, E. Suresh, and Mangalam S. Nair. "Formation of novel polycyclic cage compounds through ‘uncaging’ of readily accessible higher cage compounds." Tetrahedron Letters 47, no. 32 (2006): 5775–79. http://dx.doi.org/10.1016/j.tetlet.2006.06.005.

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Marchand, Alan P. "Polycyclic Cage Compounds as Intermediates in Organic Synthesis." Synlett 1991, no. 02 (1991): 73–79. http://dx.doi.org/10.1055/s-1991-20632.

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MARCHAND, A. P. "ChemInform Abstract: Polycyclic Cage Compounds as Intermediates in Organic Chemistry." ChemInform 22, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199116317.

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Oliver, Douglas W., and Sarel F. Malan. "Medicinal chemistry of polycyclic cage compounds in drug discovery research." Medicinal Chemistry Research 17, no. 2-7 (2007): 137–51. http://dx.doi.org/10.1007/s00044-007-9044-5.

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Mallick, Lovely, Sohan Lal, Sasidharakurup Reshmi, Irishi N. N. Namboothiri, Arindrajit Chowdhury, and Neeraj Kumbhakarna. "Theoretical studies on the propulsive and explosive performance of strained polycyclic cage compounds." New Journal of Chemistry 41, no. 3 (2017): 920–30. http://dx.doi.org/10.1039/c6nj02444k.

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Bubnov, Yu N., N. Yu Kuznetsov, M. E. Gurskii, A. L. Semenova, G. D. Kolomnikova, and T. V. Potapova. "Construction of nitrogen bicyclic and cage compounds with the use of allylic organoboranes." Pure and Applied Chemistry 78, no. 7 (2006): 1357–68. http://dx.doi.org/10.1351/pac200678071357.

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It is shown that reactions of triallylborane with pyrrole, pyridines, isoquinolines, lactams, 1-pyrroline, and acetylenes offer versatile methodology for the construction of various bicyclic and polycyclic nitrogen compounds, some of which are skeletally related to important classes of alkaloids. Optically active 3-borabicyclo[3.3.1]non-6-enes are useful precursors for synthesis of chiral 3-aza- and 3-thiabicyclo[3.3.1]non-6-enes, as well as derived chiral cyclohexenoid systems. The convenient methodology for the transformation of 1-boraadamantanes into 1-azaadamantanes is also discussed.
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Reissig, Hans-Ulrich, Reinhold Zimmer, Maurice Taszarek, and Luise Schefzig. "Reaction of a Polycyclic Diketone with Lithiated Methoxyallene:Synthesis of New Functionalized Cage Compounds." Synlett 2008, no. 15 (2008): 2388. http://dx.doi.org/10.1055/s-2008-1078172.

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MARCHAND, A. P. "ChemInform Abstract: Polycyclic Cage Compounds: Reagents, Substrates, and Materials for the 21st Century." ChemInform 27, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.199628312.

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Dissertations / Theses on the topic "Polycyclic cage compounds"

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Chong, Hyun-Soon. "Explorations with Polycarbocyclic Cage Compounds." Thesis, University of North Texas, 1999. https://digital.library.unt.edu/ark:/67531/metadc2218/.

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A variety of novel cage-functionalized pyridyl containing crown ethers have been prepared for use in selective alkali metal complexation studies. A highly preorganized, cage-functionalized cryptand also has been designed and has been synthesized for use as a selective Li+ complexant. The alkali metal picrate extraction profiles of these cage-functionalized crown ethers also have been studied. Novel cage-functionalized diazacrown ethers have been prepared for selective alkali metal complexation studies. Alkali metal picrate extraction experiments have been performed by using this new class of s
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Wang, Yanjun. "The Synthesis and Chemistry of Polyciclic Cage Compounds." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc278447/.

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Chapter I describes the synthesis of a trishomocubyl helical tubuland diol and some aspects of its inclusion chemistry. Thus, all three isomers of 4,7-dimethylpentacyclo[6.3.0.0^2,6.0^3,10.0^5,9]undecane-4,7-diol have been prepared and their X-ray structures have been determined. The syn,syn-isomer crystallizes in a double-stranded hydrogen-bonded lattice, while anti,syn-isomer forms a hydrogen-bonded layer lattice. In contrast, the anti,anti-isomer is a new member of the helical tubuland diol host family; its crystal lattice consists of parallel canals with a trefoil-shaped cross-section of a
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Jin, Pei-Wen. "Synthesis and Structure of Polynitro- and Polymenthylpolycyclic "Cage" Monomers and Polymers." Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc332109/.

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The objective of this study was to synthesize and characterize new energetic polycyclic "cage" compounds. As part of a program involved in the synthesis of new polynitropolycyclic compounds, 2,6-dinitro-5-methoxy- 7-carbomethoxypentacyclo[5. 3 .0 . 0* • * . CP • i ° . 0* •8]decane has been synthesized. This is a model system which can be used to study (1) the effect of nitro substitution on the photolability of carbon-carbon double bonds and (2) to develop methods for avoiding Haller-Bauer cleavage in cage /3-keto esters when synthesizing polynitro-substituted cage compounds.
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Ren, Chien-Tai. "Synthesis of Polycyclic "Cage" Molecules." Thesis, University of North Texas, 1989. https://digital.library.unt.edu/ark:/67531/metadc500575/.

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The synthesis of a novel, cage spiro-oxetane was carried out. Pentacyclo[5.4.0.0^2,6.0^3,10.0^5,9]undecane-8- one (PCUD-8-one) undergoes one-carbon homologation to a mixture of endo- and exo- PCUD-carboxaldehydes which then are converted into 8,8-bis(hydroxymethyl)PCUD. The monotosylate obtained via reaction of 8,8- bis(hydroxymethyl)PCUD with tosyl chloride(1 equivalent) reacts with sodium hydride to afford the corresponding spiro-oxetane via intramolecular Williamson reaction. Six new substituted heptacyclo[6.6.0.0^2,6.0^3,13.0^4,11. 0^5,9.0^10,14]tetradecanes (HCTD) were synthesized. These
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Zhao, Dalian. "Syntheses and the Structures of Polymethylpolycyclic and Polycyclic "Cage" Molecules." Thesis, University of North Texas, 1989. https://digital.library.unt.edu/ark:/67531/metadc500344/.

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The structures of Diels-Alder cycloaddition of cyclopentadiene to 2,6-dimethyl-p-benzoquinone and methylcyclopentadiene to 2,6-dimethyl-p-benzoquinone were assigned by analysis of 1-D and 2-D proton and carbon-13 NMR spectra. The structures of the cycloadduct of methylcyclopentadiene to 2,6-dimethyl-p-benzoquinone and that of the corresponding intramolecular [2+2] photocyclization product were also obtained by single crystal X-ray structural analysis. As the second part of the study, a new polycyclic "cage" molecule, a substituted trishomocubane isomer, was synthesized. In this synthesis, redu
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Abaniwonda, Modupe. "Polycyclic compounds as carriers for neuroactive non- steroidal anti-inflammatory drugs." University of the Western Cape, 2017. http://hdl.handle.net/11394/5693.

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Magister Pharmaceuticae - MPharm<br>Recent scientific findings have highlighted the beneficial roles of polycyclic cage compounds in neurodegenerative disorders such as Alzheimer's and Parkinson's diseases. Further interest into the chemistry of these compounds is stimulated by their remarkable ability to improve the pharmacokinetics profile of known neuroprotective agents. As potent lipophilic scaffolds, they can be employed to target the brain delivery of desired compounds. Inflammation is a key mediator of neuronal cell's degeneration as activated microglia and other inflammatory mediators
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Prins, Louis Hendrik Albertus. "Polycyclic cage compounds as carrier molecules for neuroprotective non-steroidal anti-inflammatory drugs / Louis H.A. Prins." Thesis, North-West University, 2007. http://hdl.handle.net/10394/1479.

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Joubert, Jacques. "Fluorescent polycyclic ligands : strategies towards the synthesis and evaluation of fluorescently labelled receptor and enzyme ligands / Jacques Joubert." Thesis, North-West University, 2012. http://hdl.handle.net/10394/10408.

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Neurodegenerative disorders, including Alzheimer's and Parkinson's disease, and the development of neuroprotective agents have received significant research attention in recent years. Development of novel imaging techniques to study the biological mechanisms involved in the progression of these disorders have become an area of research interest. The design of novel small molecule imaging probes in combination with modem imaging techniques may provide information on neuroprotective binding site• interactions and would assist in the design of novel biological assay methods. Techniques to visuali
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Sharma, Rajan. "Synthesis & biological evaluation of neuroprotective molecules with polycyclic scaffolds." University of the Western Cape, 2017. http://hdl.handle.net/11394/6228.

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Doctor Pharmaceuticae - Dpharm<br>Among neurological disorders, many of the most devastating disorders are neurodegenerative. Modern research associates excitotoxicity to a variety of neuropathological conditions, suggesting that the neurodegenerative diseases with distinct etiologies may have excitotoxicity as a common pathway. Excitotoxicity occurs through over-stimulation of receptors for excitatory neurotransmitters like the N-methyl-D-aspartate (NMDA) receptors. Due to the relevance of NMDA receptors and excitotoxic processes, the antagonism or modulation of NMDA receptors is used as a th
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Zhang, Ruoxin. "Toward the synthesis of polycyclic aromatic compounds as nano-carbon cages." Morgantown, W. Va. : [West Virginia University Libraries], 2008. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=5617.

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Thesis (M.S.)--West Virginia University, 2008.<br>Title from document title page. Document formatted into pages; contains vii, 45 p. : ill. Includes abstract. Includes bibliographical references (p. 24-26).
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Book chapters on the topic "Polycyclic cage compounds"

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Bianchi, Thomas S., and Elizabeth A. Canuel. "Anthropogenic Markers." In Chemical Biomarkers in Aquatic Ecosystems. Princeton University Press, 2011. http://dx.doi.org/10.23943/princeton/9780691134147.003.0014.

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This chapter examines the application of anthropogenic compounds as biomarkers. Since World War II, human activities have introduced a wide array of compounds into the environment, including insecticides such as dichloro-diphenyl-trichloroethane and pesticides, halocarbons (chlorofluorocarbons), sewage products (coprostanol), and polycyclic aromatic hydrocarbons (PAHs). The chapter introduces structural features of these compounds, their distribution and transformation in the environment, and their potential use(s) as tracers. It presents examples of how relationships between anthropogenic markers and biomarkers can be used to provide information about the sources, delivery, and fate of natural organic matter in aquatic ecosystems. It introduces various emerging contaminants (personal care pharmaceutical products, caffeine, and flame retardants) and their potential use as tracers for anthropogenic organic matter in aquatic ecosystems. It describes how δ‎<sup>13</sup>C, stable isotopes of Cl and Br, and radiocarbon can be used to apportion sources of organic contaminants (e.g., PAHs and PCBs).
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Morrow, Gary W. "Biosynthesis of Alkaloids and Related Compounds." In Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0010.

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Though definitions may vary from source to source, the term alkaloid generally refers to members of a large set of naturally occurring, slightly basic (i.e., alkaline) nitrogen-containing organic compounds. Generally excluded from this group are amino acids, peptides, proteins, N-containing carbohydrates, and nitrogenous bases used in the construction of nucleotides. Though a small number are produced by animals or microorganisms, the vast majority of alkaloids are plant-produced compounds possessing a remarkably diverse range of structural features, from simple cycloaliphatic amines to highly complex polycyclic N-heterocycles. Some representative alkaloids are shown in Fig. 7.1. Alkaloid-containing plants and their extracts have been used by humans for thousands of years, mainly on the basis of their stimulant, therapeutic, or poisonous properties. References to plants containing compounds such as morphine (from opium poppies), strychnine (from seeds of the Strychnos nux-vomica tree), ephedrine (from the plant Ephedra chinensis), and coniine (from the poison hemlock plant) may be found in some of our earliest known writings. Today, it has been estimated that the health care of over 5 billion people worldwide benefits from the use of plant-based medicinal agents, many of which are alkaloids. With that in mind, it is worth noting concerns that deforestation, environmental damage, large-scale development, and unregulated harvesting programs may ultimately lead to the extinction of hundreds of known medicinal plants and perhaps even more whose medicinal properties have yet to be discovered, thereby endangering the prospects for future discoveries of new curative agents for the benefit of all humankind. As a scientific field, alkaloid chemistry itself dates back to the early 1800s with the first isolation of pure crystalline morphine from opium. This milestone achievement allowed the delivery of accurate, therapeutic doses of a drug that was immensely valuable for the relief of pain but which could also lead to fatal overdoses when administered from simple extracts of variable composition and strength. The subsequent rapid development of increasingly sophisticated techniques for the isolation and purification of the active components (often alkaloids) from many other medicinal plants essentially spawned the field of organic chemistry.
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Conference papers on the topic "Polycyclic cage compounds"

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Olsen, L., L. Jaycox, and C. Neumeister. "71. Development of Analytical Methods for Polycyclic Aromatic Compounds and Sulfur Compounds in Asphalt Fume." In AIHce 1996 - Health Care Industries Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765184.

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Hanley, K., D. Almaguer, G. Burr, and K. Wallingford. "72. Field Testing Analytical Methods for Polycyclic Aromatic Compounds and Sulfur Compounds During Conventional and Crumb-Rubber-Modified Asphalt Paving." In AIHce 1996 - Health Care Industries Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765185.

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