Relevant bibliographies by topics / Polycyclic

Academic literature on the topic 'Polycyclic'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Polycyclic"

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Ati, Estabraq Mohammed. "The Seasonal Variations of Polycyclic Aromatic Hydrocarbon Polycyclic: A Review." International Journal of Psychosocial Rehabilitation 24, no. 4 (February 28, 2020): 4877–83. http://dx.doi.org/10.37200/ijpr/v24i4/pr201587.

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Boben, M., and T. Pisanski. "Polycyclic configurations." European Journal of Combinatorics 24, no. 4 (May 2003): 431–57. http://dx.doi.org/10.1016/s0195-6698(03)00031-3.

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Barton, John W., and David J. Rowe. "Polycyclic biphenylenes." Tetrahedron 41, no. 7 (January 1985): 1323–28. http://dx.doi.org/10.1016/s0040-4020(01)96534-2.

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Fariña, Francisco, M. Carmen Paredes, and Valter Stefani. "Polycyclic hydroxyquinones." Tetrahedron 42, no. 15 (January 1986): 4309–18. http://dx.doi.org/10.1016/s0040-4020(01)87657-2.

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Ayyangar, N. R., S. V. Joshi, K. V. Srinivasan, V. G. Puranik, S. S. Tavale, and T. N. Guru Row. "Polycyclic compounds." Dyes and Pigments 7, no. 2 (January 1986): 81–92. http://dx.doi.org/10.1016/0143-7208(86)85001-x.

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Assmann, Björn, and Bettina Eick. "Computing polycyclic presentations for polycyclic rational matrix groups." Journal of Symbolic Computation 40, no. 6 (December 2005): 1269–84. http://dx.doi.org/10.1016/j.jsc.2005.05.003.

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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-phosphorus atoms exhibit a low reactivity in comparison to their out-counterparts. Nevertheless some few examples of reactions at in-positioned phosphorus atoms have been presented. This will potentially open the way to a specific modification of the cavity of such macrobi- and polycyclic compounds. A review with 53 references.
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Berger, Reinhard, Manfred Wagner, Xinliang Feng, and Klaus Müllen. "Polycyclic aromatic azomethine ylides: a unique entry to extended polycyclic heteroaromatics." Chemical Science 6, no. 1 (2015): 436–41. http://dx.doi.org/10.1039/c4sc02793k.

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Donadze, G., M. Ladra, and P. Páez-Guillán. "Schur's theorem and its relation to the closure properties of the non-abelian tensor product." Proceedings of the Royal Society of Edinburgh: Section A Mathematics 150, no. 2 (January 26, 2019): 993–1002. http://dx.doi.org/10.1017/prm.2018.150.

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AbstractWe show that the Schur multiplier of a Noetherian group need not be finitely generated. We prove that the non-abelian tensor product of a polycyclic (resp. polycyclic-by-finite) group and a Noetherian group is a polycyclic (resp. polycyclic-by-finite) group. We also prove new versions of Schur's theorem.
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Chen, Yuan-Yuei, Tung-Wei Kao, Chung-Ching Wang, Chen-Jung Wu, Yi-Chao Zhou, and Wei-Liang Chen. "Association between polycyclic aromatic hydrocarbons exposure and bone turnover in adults." European Journal of Endocrinology 182, no. 3 (March 2020): 333–41. http://dx.doi.org/10.1530/eje-19-0750.

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Background Cigarette smoking is a risk factor of osteoporosis and bone fracture. Tobacco smoke contains several polycyclic aromatic hydrocarbons. Thus, we hypothesized that environmental polycyclic aromatic hydrocarbon exposure is associated with bone loss and fracture risk. The present study examined the association between polycyclic aromatic hydrocarbon exposure and bone turnover in the general adult population. Methods A total of 1408 eligible participants from the National Health and Nutrition Examination Survey (NHANES 2001–2006) were included in this cross-sectional analysis. The levels of urinary N-telopeptide and serum bone-specific alkaline phosphatase, which are biomarkers of bone resorption and formation, respectively, were assessed. Meanwhile, polycyclic aromatic hydrocarbon exposure was evaluated using the concentrations of urinary polycyclic aromatic hydrocarbon metabolites. The association between polycyclic aromatic hydrocarbon exposures and N-telopeptide, and bone-specific alkaline phosphatase levels was assessed using a multivariate linear regression model. Results All polycyclic aromatic hydrocarbon metabolites except 3-phenanthrene were significantly associated with increased N-telopeptide levels (P < 0.05) after adjustment of relevant covariables. However, no significant relationship was observed between polycyclic aromatic hydrocarbon metabolites and bone-specific alkaline phosphatase levels. This relationship remained significant after the participants were assessed according to sex (P < 0.05). Additionally, all polycyclic aromatic hydrocarbon metabolites showed a positive association with N-telopeptide levels in participants aged <60 years (P < 0.05). Conclusion Polycyclic aromatic hydrocarbon exposure is associated with increased bone resorption among the general adult population in the United States. Further studies must assess the potential mechanisms associated with the adverse effects of polycyclic aromatic hydrocarbon exposure on bone loss.
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Dissertations / Theses on the topic "Polycyclic"

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Reginato, Nada McGlinchey Michael J. "Polycyclic compounds of manganese /." *McMaster only, 2003.

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Edwards, W. D. "Synthesis of polycyclic orthoamides." Thesis, University of Manchester, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370413.

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Tian, Zhenjiao. "Oxidation and Reduction Process for Polycyclic Aromatic Hydrocarbons and Nitrated Polycyclic Aromatic Hydrocarbons." The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1228333650.

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Freeman, David John. "Polycyclic aromatic compounds in flames." Thesis, University of Cambridge, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308234.

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Billington, Helen. "Novel approaches to polycyclic heterocycles." Thesis, University of Liverpool, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.272632.

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Williams, David Alan John. "Radical approaches toward polycyclic alkaloids." Thesis, University of York, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323499.

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Crofts, Gavin Andrew. "Polycyclic peptides as host molecules." Thesis, University of York, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304170.

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Crowley, Colin. "Fullerenes from polycyclic aromatic hydrocarbons." Thesis, University of Sussex, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360582.

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Houlsby, Ian. "Asymmetric syntheses of polycyclic amines." Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:7c73384d-da09-41ee-b1fc-4509dd20aaf8.

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This thesis centers on the asymmetric synthesis of polycyclic amines, focussing on three distinct classes of polycyclic alkaloid natural products. The work aims to use common methodology of lithium amide conjugate additions as the source of asymmetry in all cases, and for each product class a single strategy is used to synthesise a variety compounds. Chapter 1 describes the importance of the synthesis of polycyclic alkaloids, highlighting three classes of compounds and documenting prior synthetic strategies. The classes discussed are: the Hancock alkaloids, hydroxymethyl-substituted azabicycles, and the tetraponerine alkaloids. Chapter 2 describes two separate synthetic strategies towards the Hancock alkaloid (-)-cuspareine, one using a benzyne mediated cyclisation and one a Buchwald-Hartwig cyclisation. The Buchwald-Hartwig methodology was also applied in the synthesis of two more Hancock alkaloids (-)-galipinine and (-)-galipeine; the synthesis of (-)-galipeine led to a reassignment of the structure of the natural product. Chapter 3 describes work in the synthesis of four [x.y.0]-azabicycles with differing in ring sizes (x, y = 3, 4). The strategy employs sequential SN2-like ring-closing reactions to form the bicyclic structures where pyrrolizidine, indolizidine and quinolizidine scaffolds can be accessed. Amongst the products are two natural alkaloids, (-)-lupinine and (+)-isoretronecanol. Chapter 4 describes the synthesis of all eight tetraponerine alkaloids T1-8. Two sequential lithium amide conjugate addition reactions allow for the synthesis of the differing ring-sizes and diastereoisomers displayed by the eight alkaloids. Ring-closing metathesis and diamine condensation with 4-bromobutanal provide the ring-closing steps in the syntheses. Chapter 5 contains full experimental procedures and characterisation data for all compounds synthesised in Chapters 2-4.
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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 compounds will be used as substrates in a photoelectron spectroscopic study. The ring-expansion reaction of PCUD-8-one with ethyl diazoacetate in the presence of BF_3:OEt_2 was performed. The major product was converted into an alcohol, and the structure of the 3,5-dinitrobenzoate of this alcohol was elucidated by single crystal x-ray structural analysis.
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Books on the topic "Polycyclic"

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Harvey, Ronald G. Polycyclic aromatic hydrocarbons. New York: Wiley-VCH, 1997.

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Hayakawa, Kazuichi, ed. Polycyclic Aromatic Hydrocarbons. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4.

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Shen, Huizhong. Polycyclic Aromatic Hydrocarbons. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49680-0.

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Polycyclic aromatic hydrocarbons. New York: Wiley-VCH, 1997.

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Dias, Jerry Ray. Handbook of polycyclic hydrocarbons. Oxford: Elsevier, 1988.

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Dias, Jerry Ray. Handbook of polycyclic hydrocarbons. Amsterdam: Elsevier, 1987.

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Miao, Qian, ed. Polycyclic Arenes and Heteroarenes. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527689545.

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Hall, K. R., and K. N. Marsh, eds. Densities of Polycyclic Hydrocarbons. Berlin/Heidelberg: Springer-Verlag, 1999. http://dx.doi.org/10.1007/b71427.

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Harvey, Ronald G., ed. Polycyclic Hydrocarbons and Carcinogenesis. Washington, D.C.: American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0283.

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NATO Advanced Research and CNRS Workshop on Polycyclic Aromatic Hydrocarbons and Astrophysics (1986 Les Houches, Hauto-Savoie, France). Polycyclic aromatic hydrocarbons and astrophysics. Dordrecht: D. Reidel Pub. Co., 1987.

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Book chapters on the topic "Polycyclic"

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Gooch, Jan W. "Polycyclic." In Encyclopedic Dictionary of Polymers, 556. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9021.

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Haworth, D. T., G. Y. Lin Kiel, Lee J. Todd, and Mark W. Baize. "Polycyclic Borazines." In Inorganic Syntheses, 57–60. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132609.ch17.

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Bunting, R. K. "Polycyclic Chains." In Inorganic Reactions and Methods, 91–92. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145326.ch53.

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Hayakawa, Kazuichi. "Chemistry of Polycyclic Aromatic Hydrocarbons (PAHs), Nitropolycyclic Aromatic Hydrocarbons (NPAHs) and Other Oxidative Derivatives of PAHs." In Polycyclic Aromatic Hydrocarbons, 3–10. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_1.

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Chetiyanukornkul, Thaneeya, Thanyarat Chuesaard, Akira Toriba, and Kazuichi Hayakawa. "Atmospheric Polycyclic Aromatic Hydrocarbons and Nitropolycyclic Aromatic Hydrocarbons in Thailand." In Polycyclic Aromatic Hydrocarbons, 117–36. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_10.

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Pham, Chau Thuy. "Polycyclic Aromatic Hydrocarbons and Nitropolycyclic Aromatic Hydrocarbons in Motorcycle Exhaust." In Polycyclic Aromatic Hydrocarbons, 137–53. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_11.

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Nassar, Hossam F. "Emission Sources of Polycyclic Aromatic Hydrocarbons/Nitropolycyclic Aromatic Hydrocarbons in Cairo, Egypt, Including Source Markers." In Polycyclic Aromatic Hydrocarbons, 155–62. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_12.

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Inomata, Yayoi. "Model Simulations of PAHs in Northeast Asia." In Polycyclic Aromatic Hydrocarbons, 163–71. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_13.

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Chizhova, T., Yu Koudryashova, P. Tishchenko, and V. Lobanov. "PAHs in the Northwestern Japan Sea." In Polycyclic Aromatic Hydrocarbons, 175–202. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_14.

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Hayakawa, Kazuichi. "Polycyclic Aromatic Hydrocarbons in the Southeastern Japan Sea." In Polycyclic Aromatic Hydrocarbons, 203–11. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_15.

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Conference papers on the topic "Polycyclic"

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Berné, O., C. Joblin, G. Mulas, A. G. G. M. Tielens, and J. R. Goicoechea. "Polycyclic Aromatic Hydrocarbons with SPICA." In SPICA joint European/Japanese Workshop. Les Ulis, France: EDP Sciences, 2009. http://dx.doi.org/10.1051/spica/200903005.

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REYMOND, JEAN-LOUIS. "PEPTIDE DENDRIMERS AND POLYCYCLIC PEPTIDES." In 23rd International Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2014. http://dx.doi.org/10.1142/9789814603836_0003.

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Pyrko, A. N., and M. V. Smolnik. "SYNTHESIS OF NEW POLYCYCLIC PYRIDINE DERIVATIVES." In SAKHAROV READINGS 2020: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. Minsk, ICC of Minfin, 2020. http://dx.doi.org/10.46646/sakh-2020-2-158-161.

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Wong, Wallace W. H. "Polycyclic aromatic hydrocarbons for organic photovoltaics." In Asia Communications and Photonics Conference and Exhibition. Washington, D.C.: OSA, 2011. http://dx.doi.org/10.1364/acp.2011.83120j.

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Wong, Wallace W. "Polycyclic aromatic hydrocarbons for organic photovoltaics." In SPIE/OSA/IEEE Asia Communications and Photonics, edited by Min Gu. SPIE, 2011. http://dx.doi.org/10.1117/12.902704.

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Rastogi, Shantanu, Amit Pathak, and Anju Maurya. "Polycyclic aromatic hydrocarbon molecules in astrophysics." In FIRST INTERNATIONAL CONFERENCE ON CHEMICAL EVOLUTION OF STAR FORMING REGION AND ORIGIN OF LIFE: Astrochem2012. AIP, 2013. http://dx.doi.org/10.1063/1.4812599.

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Steber, Amanda, Melanie Schnell, Daniël Rap, and Cristobal Perez. "MOLECULAR HYDROGEN COMPLEXATION WITH POLYCYCLIC AROMATIC HYDROCARBONS." In 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.wj06.

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Mangione-Smith, William, Santosh G. Abraham, and Edward S. Davidson. "Vector register design for polycyclic vector scheduling." In the fourth international conference. New York, New York, USA: ACM Press, 1991. http://dx.doi.org/10.1145/106972.328664.

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Viecelli, N. C., E. R. Lovatel, E. M. Cardoso, and I. N. Filho. "Degradation of polycyclic aromatic hydrocarbons in soil." In International Conference on Environmental Science and Biological Engineering. Southampton, UK: WIT Press, 2014. http://dx.doi.org/10.2495/esbe140371.

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Bargeron, C. Brent, Richard C. Benson, Terry E. Phillips, Peter F. Scholl, Sala Abubaker, John D. Groopman, and Paul T. Strickland. "Immunoaffinity-based biosensor for polycyclic aromatic hydrocarbons." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Gerald E. Cohn. SPIE, 2001. http://dx.doi.org/10.1117/12.426743.

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Reports on the topic "Polycyclic"

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Sander, Lane C., Lane C. Sander, and Stephen A. Wise. Polycyclic aromatic hydrocarbon structure index. Gaithersburg, MD: National Institute of Standards and Technology, 1997. http://dx.doi.org/10.6028/nist.sp.922.

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Sander, Lane C., and Stephen A. Wise. Polycyclic aromatic hydrocarbon structure index. Gaithersburg, MD: National Institute of Standards and Technology, August 2020. http://dx.doi.org/10.6028/nist.sp.922e2020.

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Nguyen, Tuan Hoang. Synthesis of Polycyclic Natural Products. Office of Scientific and Technical Information (OSTI), January 2003. http://dx.doi.org/10.2172/815761.

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Allison, Thomas C., and Donald R. Burgess Jr. Thermodynamic Properties of Polycyclic Aromatic Hydrocarbons. National Institute of Standards and Technology, December 2015. http://dx.doi.org/10.6028/nist.sp.1186.

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Huncik, Kevin M., John Kucklick, and Jared M. Ragland. Polycyclic aromatic hydrocarbons (PAHs) in marine mammal blubber:. Gaithersburg, MD: National Institute of Standards and Technology, March 2019. http://dx.doi.org/10.6028/nist.ir.8233.

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Moriarty, Robert M. Alkyl Azides, Diazides, Haloazides and Bridged Polycyclic Diazides. Fort Belvoir, VA: Defense Technical Information Center, May 1991. http://dx.doi.org/10.21236/ada236202.

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Steele, W. V., R. D. Chirico, and T. D. Klots. Thermodynamic properties for polycyclic systems by non-calorimetric methods. Office of Scientific and Technical Information (OSTI), March 1993. http://dx.doi.org/10.2172/6630201.

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Atanassova, Irena, Milena Harizanova, and Matrin Banov. Labile Polycyclic Aromatic Hydrocarbons (PAHs) in Fly Ash Reclaimed Technosols. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, October 2019. http://dx.doi.org/10.7546/crabs.2019.10.18.

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Harris, B. W., L. K. M. Minor, and B. J. Flucas. Polycyclic aromatic hydrocarbons at selected burning grounds at Los Alamos National Laboratory. Office of Scientific and Technical Information (OSTI), February 1998. http://dx.doi.org/10.2172/578587.

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Barofsky, D. F. [Mass spectrometric analysis of polycyclic aromatic hydrocarbons adducted to DNA]. Final report. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10112374.

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