Relevant bibliographies by topics / Synthesis of polycyclic compounds

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Synthesis of polycyclic compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Synthesis of polycyclic compounds"

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Lai Chan, Wing, Chok Wah Lo, Yau Shan Szeto, and Chiu Wing Yip. "Synthesis of Polycyclic Bismesoionic Compounds." HETEROCYCLES 51, no. 6 (1999): 1433. http://dx.doi.org/10.3987/com-99-8507.

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Sakakibara, Makoto, Takahiro Mizumoto, Yoshihiko Watanabe, Takeshi Toru, and Yoshio Ueno. "Synthesis of Novel Polycyclic Selenepinone Compounds." Bulletin of the Chemical Society of Japan 65, no. 7 (July 1992): 1794–98. http://dx.doi.org/10.1246/bcsj.65.1794.

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Nadaf, Ankusab Noorahmadsab, and Kalegowda Shivashankar. "Visible Light Assisted Hantzsch Reaction: Synthesis of Polycyclic Dihydropyridines." Letters in Organic Chemistry 16, no. 8 (June 18, 2019): 676–82. http://dx.doi.org/10.2174/1570178615666181107095151.

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The polycyclic dihydropyridine nucleus represents the heterocyclic system of invaluable core motifs with wide applications in chemical, biological and physical properties. Although this kind of compounds have been extensively synthesized by other groups, the synthesis of these compounds under CFL light intensity were not explored. The synthesis of polycyclic dihydropyridine derivatives were achieved through the reaction of 4-hydroxycoumarin, aromatic aldehydes and ammonium acetate under CFL light irradiation conditions. A series of polycyclic dihydropyridine derivatives were prepared under CFL light irradiation conditions with high yield, short reaction time, ambient condition and without the use of catalyst. The results displayed an efficient method for the synthesis of polycyclic dihydropyridine derivatives. Clean profile, short reaction time, low cost and use of CFL light intensity instead of catalyst making it a genuinely green protocol.
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YAMAGUCHI, Masahiko. "Synthesis of polycyclic aromatic compounds via polyketides." Journal of Synthetic Organic Chemistry, Japan 45, no. 10 (1987): 969–82. http://dx.doi.org/10.5059/yukigoseikyokaishi.45.969.

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Masusai, Chonticha, Darunee Soorukram, Chutima Kuhakarn, Patoomratana Tuchinda, Chaveng Pakawatchai, Saowanit Saithong, Vichai Reutrakul, and Manat Pohmakotr. "Synthesis of gem-Difluoromethylenated Polycyclic Cage Compounds." Journal of Organic Chemistry 80, no. 3 (January 26, 2015): 1577–92. http://dx.doi.org/10.1021/jo502501v.

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Tominaga, Yoshinori, Kenji Sasaki, and Raymond N. Castle. "Synthesis of polycyclic pyridazinediones as chemiluminescent compounds." Journal of Heterocyclic Chemistry 35, no. 5 (September 1998): 1219–34. http://dx.doi.org/10.1002/jhet.5570350516.

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Toyota, Masahiro. "Synthesis of Polycyclic Compounds Employing Palladium-catalyzed Cycloalkenylation." Journal of Synthetic Organic Chemistry, Japan 64, no. 1 (2006): 25–33. http://dx.doi.org/10.5059/yukigoseikyokaishi.64.25.

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Harvey, Ronald. "Advances in the Synthesis of Polycyclic Aromatic Compounds." Current Organic Chemistry 8, no. 4 (March 1, 2004): 303–23. http://dx.doi.org/10.2174/1385272043485918.

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Li, Ang, Daniel J. DeSchepper, and Douglas A. Klumpp. "Triflic acid promoted synthesis of polycyclic aromatic compounds." Tetrahedron Letters 50, no. 17 (April 2009): 1924–27. http://dx.doi.org/10.1016/j.tetlet.2009.02.042.

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Pei, J., W. Y. Zheng, J. Mao, and X. H. Zhou. "Efficient Synthesis of Thiophene-Based Polycyclic Aromatic Compounds." Synfacts 2006, no. 5 (May 2006): 0445. http://dx.doi.org/10.1055/s-2006-934384.

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Dissertations / Theses on the topic "Synthesis of polycyclic compounds"

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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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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 area 25.4 Å^2. Chapter II describes the synthesis of new molecular clefts. These molecular clefts have been synthesized via base-promoted reactions of 3,6-diaryl-l,2,4,5-tetrazines with tetracyclo[6.3.0.0^4,11.0^5,9]undecane-3,6-dione and with tricyclo[6.3.0.0^2,6]undecane-3,11-dione, respectively. Compounds of this type are of interest as a potential new class of host molecules for use in host-guest complexation studies. Chapter III reports the synthesis of stereospecifically deuterated spiro(oxetane-3,8'-pentacyclo[5.4.0.0^2,6.0^3,10.0^5,9]undecanes) and their acid-promoted ring opening and concomitant rearrangements. The deuterium-containing reaction products have been characterized via analysis of their NMR and mass spectra. The results strongly suggest that intramolecular 1,5-hydride shifts provide an important pathway through which the acid promoted rearrangements occur. Chapter IV reports the oxidation of heptacyclo-[6.6.0.0^2,6.0^3,13.0^4,11.0^5,9.0^10,14] tetradecane (HCTD) via application of Barton's "GoAgg" systems. The products have been characterized by NMR and mass spectral analysis. Under GoAgg^v conditions, oxidation of HCTD proceeds to afford heptacyclo [6.6.0.0^2,6.0^3,13.0^4,11.0^5,9.0^10,14]tetradecan-7-one in 1% yield.
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Torres, Costa Eva. "Synthesis of polycyclic compounds with antiviral activity." Doctoral thesis, Universitat de Barcelona, 2013. http://hdl.handle.net/10803/124040.

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Research for new antivirals to treat Influenza A virus infections has gained importance during this last decade due to the imminent danger of an Influenza pandemic. For some years, several new strains of this virus have appeared worldwide causing small outbreaks with a notable relevance, for example the ‘avian flu’ (H5N1 in 2007; H7N9 in 2012) and ‘swine flu’ (H1N1 in 2009), that have triggered the assumption that a new pandemic is coming. There are several strategies to treat an Influenza A virus infection targeting some of its surface proteins. In this Thesis, several compounds inhibiting the M2 channel of the virus are designed, synthesized and evaluated. Our approach is based on the synthesis of amantadine’s analogues by ring expansion, contraction and rearrangement. Amantadine is a drug already approved by the FDA for the treatment of Influenza A virus and it is known to target the M2 channel. Although it is no longer in use, because the FDA has recommended against its use, due to the appearance of resistance, it possessed good activity and an acceptable pharmacological behaviour. Our main goal was to synthesize an analogue of amantadine that was able to overcome the resistant virus and provide a new therapeutic alternative to the already marketed neuraminidase inhibitors such as Oseltamivir and Zanamivir. Importantly, we took advantage of the wide expertise of our research group in synthesizing polycyclic compounds to start a new research field that was based on the application of these optimized synthetic routes to the Medicinal chemistry. We established some external collaboration in order to set up the milestones and to build the rationale of the current project. These new collaborations are the following: - Prof. Lieve Naesens research group in the Rega Institute for Medical Research in Leuven, Belgium. This group of virologist made the plaque reduction assays and the study of the mutants to establish the mechanism of action of the tested compounds. - Lawrence H. Pinto research group of the Northwestern University, Evanston, Illinois, USA. This group of biochemist made the patch clamp assay to check if our compounds targeted the M2 channel. - Prof. Javier Luque of Universitat de Barcelona, Barcelona, España. This group made the docking and molecular dynamics of our compounds. In the following figures, the general structures of the compounds synthesized in the current Thesis are shown. Several of them showing an outstanding activity that allowed us to publish in the most important journals of the Medicinal Chemistry field: It it worth to mention that, several compounds have shown better activity than the reference compound, Amantadine. The most distinguished compounds are the following: Compound 1, 2 and 3 showed a superior activity against H1N1 strain in the cell culture assay while being almost inactive in the patch clamp assay. Prof. Lieve Naesen’s research group tried to identify the mechanism of action of these compounds selecting the mutants of hemagglutinin under the pressure of our compounds, revealing that this protein was the target of the first cluster of molecules. Compound 4 and 5 showed an outstanding activity against the wild-type and V27A M2 channels of influenza A virus. Taken together, all of these results show that tuning the polycyclic scaffold of amantadine could be the way to overcome the already stated resistance. A second part of this current Thesis consisted in a collection of compounds that have activity against vaccinia virus. These compounds are analogues of Tecovirimat®, a compound that it is currently in phase III clinical trials. When we started this project, we wanted to explore the impact in the EC50 of changing the polycyclic scaffold of the Tecovirimat® molecule, a common tool used in Medicinal Chemistry. We synthesized nearly 40 compounds and we obtained activities similar to Tecovirimat®, although none of our molecules was better than the reference compound.
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Murrison, Sarah Louise. "Diversity-oriented synthesis of polycyclic alkaloid-like compounds." Thesis, University of Leeds, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531520.

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Wu, An-hsiang. "Syntheses of Highly Strained Energetic Molecules and Development of New Synthetic Methodology." Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc331132/.

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The objective of this study was to synthesize new energetic, strained, saturated polycyclic compounds. For this purpose, new methodology has been developed, as follows: (i) Ketenes have been generated in situ via treatment of aldo-, keto- or alkenoic acid with either toluenesulfonyl chloride or 2-chloro-1-methylpyridfniurn iodide (Mulkaiyama's reagent). The reactive intermediates thereby generated have been found to undergo intramolecular [2+2] cycloaddition reactions in these systems.
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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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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, reductive bond cleavage followed by Dieckmann condensation was employed. Wolff-Kishner reduction then was used to convert a β-keto ester "cage" molecule to the corresponding carboxylic acid. A compound that possesses twofold symmetry was isolated from reaction product mixture. The structure of this compound has been established by single crystal X-ray crystallography.
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Cho, Don Mark. "Partially fluorinated polycyclic aromatic compounds synthesis and supramolecular behavior /." Lexington, Ky. : [University of Kentucky Libraries], 2006. http://lib.uky.edu/ETD/ukychem2007t00544/Cho_thesis.pdf.

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Thesis (M.S.)--University of Kentucky, 2006.
Title from document title page (viewed on February 27, 2007). Document formatted into pages; contains: xiv, 69 p. : ill. (some col.). Includes abstract and vita. Includes bibliographical references (p. 64-68).
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Cho, Don Mark. "PARTIALLY FLUORINATED POLYCYCLIC AROMATIC COMPOUNDS: SYNTHESIS AND SUPRAMOLECULAR BEHAVIOR." UKnowledge, 2007. http://uknowledge.uky.edu/gradschool_theses/443.

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The field of organic electronics has received much attention over the last few years, and engineering of organic crystals to grow with pi-electron systems arranged in a face-to-face motif has been shown to be beneficial in electronic devices. The effects of combining aromatic and perfluorinated aromatic derivatives have shown that the intramolecular stacking pattern can be changed from an edge-to-face arrangement to that of a face-to-face motif. Before the work described herein, there were no reported studies of the supramolecular behavior of fused polycyclic aromatic compounds with partial peripheral fluorination, inducing the desired face-to-face behavior. This is the main focus of the thesis. Furthermore, by exploiting the interactions between the fluorinated and non-fluorinated faces of the molecule, columnar liquid crystalline behavior can be achieved through variations of the alkyl substituents on the molecule.
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Chaolumen. "Synthesis and Properties of Electron-Deficient Polycyclic Aromatic Compounds." 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225617.

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Books on the topic "Synthesis of polycyclic compounds"

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Pfeffer, Michel, and Jairton Dupont. Palladacycles: Synthesis, characterization and applications. Weinheim: Wiley-VCH, 2008.

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Ohta, Yusuke. Copper-catalyzed multi-component reactions: Synthesis of nitrogen-containing polycyclic compounds. Berlin: Springer Verlag, 2011.

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International Symposium on Polynuclear Aromatic Hydrocarbons (13th 1991 Bordeaux, France). Polycyclic aromatic compounds: Synthesis, properties, analytical measurements, occurrence, and biological effects : proceedings of the 13th International Symposium on Polynuclear Aromatic Hydrocarbons, October 1-4, 1991, Bordeaux. Yverdon, Switzerland: Gordon and Breach Science, 1993.

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International, Symposium on Polynuclear Aromatic Hydrocarbons (11th 1987 Gaithersburg Md ). Polynuclear aromatic hydrocarbons: Measurements, means, and metabolism. Columbus, Ohio: Battelle Press, 1991.

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Karcher, W., ed. Spectral Atlas of Polycyclic Aromatic Compounds. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1263-2.

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Karcher, W., J. Devillers, Ph Garrigues, and J. Jacob, eds. Spectral Atlas of Polycyclic Aromatic Compounds. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-2668-7.

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

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IARC Working Group on the Evaluation of the Carcinogenic Risk of Chemicals to Humans (1984 Lyon, France). Polynuclear aromatic compounds. [Lyon, France]: International Agency for Research on Cancer, 1985.

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International In Situ and On-Site Bioremediation Symposium (5th 1999 San Diego, Calif.). Bioremediation technologies for polycyclic aromatic hydrocarbon compounds. Edited by Leeson Andrea 1962- and Alleman Bruce C. 1957-. Columbus, Ohio: Battelle Press, 1999.

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Adelosoye, Adekemi M. Synthesis of azacrown compounds. Manchester: UMIST, 1993.

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Book chapters on the topic "Synthesis of polycyclic compounds"

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Sygula, Andrzej, and Peter W. Rabideau. "Synthesis and Chemistry of Polycyclic Aromatic Hydrocarbons with Curved Surfaces: Buckybowls." In Carbon-Rich Compounds, 529–65. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527607994.ch12.

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Wu, Jishan, and Klaus Müllen. "All-benzenoid Polycyclic Aromatic Hydrocarbons: Synthesis, Self-assembly and Applications in Organic Electronics." In Carbon-Rich Compounds, 90–139. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527607994.ch3.

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Garms, C., and W. Francke. "Syntheses of 13C-Labelled Polycyclic Aromatic Compounds." In Treatment of Contaminated Soil, 95–131. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-662-04643-2_9.

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Yamada, Koji, Kentaro Abe, Masafumi Mikami, Morihiro Saito, and Jun Kuwano. "Synthesis of Carbon Nanotubes from Polycyclic Compounds by CVD Method." In Electroceramics in Japan IX, 163–66. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-411-1.163.

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Vogel, Pierre. "Combinatorial Synthesis of Linearly Condensed Polycyclic Compounds, Including Anthracyclinones, Through Tandem Diels–Alder Additions." In Anthracycline Chemistry and Biology I, 187–214. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/128_2007_148.

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Šimko, Peter. "Polycyclic Aromatic Hydrocarbons." In Analysis of Endocrine Disrupting Compounds in Food, 429–45. Oxford, UK: Wiley-Blackwell, 2012. http://dx.doi.org/10.1002/9781118346747.ch19.

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Stolar, Monika, and Thomas Baumgartner. "P-Containing Heteroarenes: Synthesis, Properties, Applications." In Polycyclic Arenes and Heteroarenes, 309–30. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527689545.ch12.

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Nay, Bastien, and Nassima Riache. "Biomimetic Synthesis of Non-Aromatic Polycyclic Polyketides." In Biomimetic Organic Synthesis, 503–35. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634606.ch14.

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Keese, R., W. Luef, J. Mani, S. Schüttel, M. Schmid, and C. Zhang. "Planarizing Distortions in Polycyclic Carbon Compounds." In Strain and Its Implications in Organic Chemistry, 283–96. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0929-8_20.

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Morrow, Gary W. "The Acetate Pathway: Biosynthesis of Polyketides and Related Compounds." In Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0008.

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We saw in the previous chapter how Otto Wallach’s early proposal regarding the structural origin of terpenoid natural products was later refined by the insightful work of Leopold Rudzicka, leading to the biogenetic isoprene rule and all that it implies. In a nearly parallel fashion, we find in our present chapter a second, unrelated class of naturally occurring compounds whose characteristic structural features prompted an initial innovative hypothesis by J. N. Collie near the turn of the 20th century. Collie proposed that certain natural compounds might arise from precursors containing repeated “ketide” (–CH2CO–) units which could then undergo subsequent condensations and other reactions typical of carbonyl compounds to produce some of the observed structures. Unfortunately, Collie’s work was more or less ignored and largely forgotten for nearly a half century, only to be reimagined and expanded in the middle of the century by A. J. Birch, another pioneer whose proposals met with considerable initial resistance. But unlike his predecessor, Birch ultimately prevailed by providing experimental results that supported a comprehensive theory of the biochemical origin of the group of compounds now universally known as “polyketide” natural products. This structurally diverse family includes some of the most useful medicinal agents now known to us, with many members possessing powerful antibacterial, antifungal, anticancer, immunosuppressant, and even cholesterol-lowering biological properties. As we see in Fig. 5.1, such structures range from the relatively simple to the exceedingly complex and may include large macrocyclic lactone rings (macrolides) such as erythromycin, polycyclic ethers such as monensin A, polycyclic structures which may be partly or mostly aromatic as in tetracycline, griseofulvin, or daunorubicin, or nonaromatic polycyclics such as tacrolimus and lovastatin. Some also contain noncyclic linear components that may be saturated, oxygenated, or unsaturated, as seen in different regions of amphotericin B which, like erythromycin, daunorubicin, and many other polyketides, also possesses an aglycone core which has been glycosylated with a carbohydrate component at a specific position. But in spite of this range of structures, many polyketide compounds share some common features that ultimately become more evident upon closer inspection; six-membered rings (either aromatic or nonaromatic) and multiple oxygens which tend to appear in a repeating 1,3-relationship to one another on both acyclic, cyclic, and aromatic structures.
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Conference papers on the topic "Synthesis of polycyclic compounds"

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Lei, Hanwu, Shoujie Ren, James Julson, Lu Wang, Quan Bu, and Roger Ruan. "Microwave Torrefaction of Corn Stover and Tech-Economic Analysis." In ASME 2011 International Manufacturing Science and Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/msec2011-50230.

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Microwave torrefaction of corn stover with particle size of 4 mm was investigated and the effects of reaction temperature and time on the yields of volatile, bio-oil and torrefied biomass were determined. The response surface analysis of the central composite design (CCD) showed that the yields of volatile, bio-oil and torrefied biomass were significantly affected by the reaction temperature and time. Three linear models were developed to predict the yields of conversion products as a function of temperature and time. A first order reaction kinetics was also developed to model the corn stover torrefaction. Ph values of torrefaction bio-oils ranged from 2.3 to 2.76 which were similar to those of bio-oils from biomass pyrolysis. GC/MS analysis for torrefaction bio-oils showed that the organic acid was about 2.16% to 12.00%. The torrefaction bio-oils also contain valuable chemical compounds such as phenols, furan derivatives and aliphatic hydrocarbons determined by a GC/MS. There are no aromatic compounds and polycyclic aromatic hydrocarbons (PAHs) detected in the torrefaction bio-oils. The torrefaction biogas was mainly consisted of ch4, c2h6, c3h8, which was about 56 wt% of the total bio-gas. The biogas can be used for chemical synthesis or electricity generation. The heating values of torrefied biomass were from 18.64–22.22 MJ/kg depending on the process conditions. The heating values of torrefied biomass were significantly greater than those of raw biomass and similar to those of coals. The energy yields of torrefied biomass from 87.03–97.87% implied that most energy was retained in the torrefied biomass. Economic analysis indicated that the biomass microwave torrefaction plant located in a farm is profitable.
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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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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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Margetić, Davor. "Synthesis of 7-silanorbornene Electron Donor-Acceptor Polycyclic Dyads." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01465.

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Takenobu, T. "Synthesis of organics/SWNT compounds." In MOLECULAR NANOSTRUCTURES: XVII International Winterschool Euroconference on Electronic Properties of Novel Materials. AIP, 2003. http://dx.doi.org/10.1063/1.1627990.

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Parekh, K., and P. B. Aswath. "Synthesis of Fluorinated ZDDP Compounds." In STLE/ASME 2006 International Joint Tribology Conference. ASME, 2006. http://dx.doi.org/10.1115/ijtc2006-12053.

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Quazi, Nurul H., Andrew B. Hughes, and Leann M. Tilley. "Synthesis of novel fluorescent compounds." In BiOS '97, Part of Photonics West, edited by Richard B. Thompson. SPIE, 1997. http://dx.doi.org/10.1117/12.273540.

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Gryaznova, M. V., Vladimir V. Danilov, A. I. Khrebtov, G. N. Ermolaeva, V. B. Shilov, and Teimur A. Shakhverdov. "Influence of radical ions on optical limiting effect in solutions of polycyclic compounds." In SPIE Proceedings, edited by Oleg B. Danilov. SPIE, 2004. http://dx.doi.org/10.1117/12.558541.

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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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Jalkian, Rafi D., and M. Bonner Denton. "HPLC Determination Of Polycyclic Aromatic Compounds By Fluorescence Detected With A Charge-Coupled Device." In OE/LASE '89, edited by E. R. Menzel. SPIE, 1989. http://dx.doi.org/10.1117/12.951546.

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Reports on the topic "Synthesis of polycyclic compounds"

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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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Zhao, G. Synthesis of organosilicon compounds. Office of Scientific and Technical Information (OSTI), January 1996. http://dx.doi.org/10.2172/453770.

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Cureton, LaShonda T., and John J. La Scala. Synthesis and Characterization of Furanic Compounds. Fort Belvoir, VA: Defense Technical Information Center, September 2013. http://dx.doi.org/10.21236/ada592103.

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Mamantov, G., and E. L. Wehry. Chemical interactions of polycyclic organic compounds with coal fly ash and related solid surfaces. Office of Scientific and Technical Information (OSTI), March 1990. http://dx.doi.org/10.2172/7030871.

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Palyulin, Vladimir A. Computer-Aided Synthesis Design of Energetic Compounds. Fort Belvoir, VA: Defense Technical Information Center, November 2008. http://dx.doi.org/10.21236/ada525358.

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Professor Monica Sorescu. SYNTHESIS AND CHARACTERIZATION OF NEW INTERMETALLIC COMPOUNDS. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/821463.

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Hoffmann, Roald, and M. J. Sienko. Thin Film Synthesis of Superconducting Chemical Compounds. Fort Belvoir, VA: Defense Technical Information Center, November 1985. http://dx.doi.org/10.21236/ada162807.

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McQuaid, Michael J., and Chiung-Chu Chen. A Computationally Based Study of Polycyclic Nitramines and Their Precursors: Comparisons between Known and Notional Compounds. Fort Belvoir, VA: Defense Technical Information Center, February 2015. http://dx.doi.org/10.21236/ada613725.

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Hirschon, A. S., M. Asaro, and J. Bottaro. Synthesis of model compounds for coal liquefaction research. Office of Scientific and Technical Information (OSTI), November 1990. http://dx.doi.org/10.2172/7113040.

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Sen, P. K. Synthesis of model compounds for coal liquification research. Office of Scientific and Technical Information (OSTI), October 1990. http://dx.doi.org/10.2172/6444779.

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