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Relevant bibliographies by topics / Oxepin

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Academic literature on the topic 'Oxepin'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Oxepin"

1

Berndt, Torsten, and Olaf Böge. "Reaction of O(3P) Atoms with Benzene." Zeitschrift für Physikalische Chemie 218, no. 4 (2004): 391–404. http://dx.doi.org/10.1524/zpch.218.4.391.29202.

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AbstractThe gas-phase reaction of O(3P) atoms with benzene was investigated in a flow system in the pressure range of 50–100mbar and a temperature of 295 ± 2K with a focus on the product formation. O2 concentrations in the carrier gas were in the range of (7.7–84) × 1014 molecule cm−3. The primary stable products detected were phenol, benzene oxide/oxepin and a not identified compound with the probable composition C5H6O. The yields of phenol and benzene oxide/oxepin were 0.12 ± 0.02 and 0.26 ± 0.06, respectively, being not affected by the experimental conditions. For benzene oxide/oxepin, a ra

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2

Florea, Stelian, Anca Nicolae, and Ovidiu Maior. "SYNTHESIS OF NEW BENZO[e]DIBENZOFURO[2,3-b]-OXEPIN-5(14H)-ONES." SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 4, no. 4 (1996): 101–8. http://dx.doi.org/10.48141/sbjchem.v4.n4.1996.101_1996.pdf.

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The new ring systems, benzo[e]dibenzofuro[2,3-b]oxepin-5(14H)-one and benzo[e]dibenzofuro[2,1-b]oxepin-5(14H)-one were obtained by cyclizing of 2-(2-dibenzoftuyloxymethyl)benzoic acid in the presence of polyphosphoric acid ester.By cyclization of the 2-(1-methoxy-2-dibenzofuryloxymethyl) benzoic acid was obtained benzo[e]dibenzofuro[2,3-b]-oxepin-12-methoxy-5-one with a indubitable structure. The structure of the new compounds was proved by means of 1H-and 13C-NMR spectra.

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Li, Ning, Binrong Yao, Chunhua Wang, Qingguo Meng, and Guige Hou. "Synthesis, crystal structure and activity evaluation of novel 3,4-dihydro-1-benzoxepin-5(2H)-one derivatives as protein–tyrosine kinase (PTK) inhibitors." Acta Crystallographica Section C Structural Chemistry 73, no. 11 (2017): 1003–9. http://dx.doi.org/10.1107/s2053229617015145.

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Four new 3,4-dihydro-1-benzoxepin-5(2H)-one derivatives, namely (E)-4-(5-bromo-2-hydroxybenzylidene)-6,8-dimethoxy-3,4-dihydrobenzo[b]oxepin-5(2H)-one, (7), (E)-4-[(E)-3-(5-bromo-2-hydroxyphenyl)allylidene]-6,8-dimethoxy-3,4-dihydrobenzo[b]oxepin-5(2H)-one, (8), (E)-4-(5-bromo-2-hydroxybenzylidene)-6-hydroxy-8-methoxy-3,4-dihydrobenzo[b]oxepin-5(2H)-one, C18H15BrO5, (9), and (E)-4-[(E)-3-(5-bromo-2-hydroxyphenyl)allylidene]-6-hydroxy-8-methoxy-3,4-dihydrobenzo[b]oxepin-5(2H)-one, (10), have been synthesized and characterized by FT–IR, NMR and MS. The structure of (9) was confirmed by single-cr

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4

Klotz, Björn, Ian Barnes, Karl H. Becker, and Bernard T. Golding. "Atmospheric chemistry of benzene oxide/oxepin." Journal of the Chemical Society, Faraday Transactions 93, no. 8 (1997): 1507–16. http://dx.doi.org/10.1039/a606152d.

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Jasinski, Jerry P., Q. N. M. Hakim Al-arique, Ray J. Butcher, H. S. Yathirajan, and B. Narayana. "6,11-Dihydrodibenz[b,e]oxepin-11-one." Acta Crystallographica Section E Structure Reports Online 66, no. 1 (2009): o159—o160. http://dx.doi.org/10.1107/s1600536809053409.

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Warrener, RN, IG Pitt, KDV Weerasuria, and RA Russell. "Acetylene Stacking: a New Concept for the Synthesis of Cyclic Polyenes. Application to the Preparation of a 1,6-Bridged Bicyclo[4.2.0]octa-2,4,7-triene and Some Novel Oxepins." Australian Journal of Chemistry 45, no. 1 (1992): 155. http://dx.doi.org/10.1071/ch9920155.

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A new protocol for a general synthesis of cyclic polyenes is presented; in this protocol two new concepts are introduced. The first, acetylene stacking, is the generic term covering both the synthesis of a target molecule and the specific retrosynthesis upon which it is based. This retrosynthetic analysis involves conversion of the target molecule, through a series of transannular [ π2s+π2s] valence isomerizations , into a key polycyclobutanoid intermediate (24). This intermediate is cleaved, in turn, through a similar number of [ σ2s+ σ2s] electrocyclic fragmentations, to yield a set of acety

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7

Wyatt, Dorothy K., Nina M. Roscher, and Lee T. Grady. "Carbon13 NMR of Z- and E-Doxepin Hydrochloride." Applied Spectroscopy 40, no. 4 (1986): 538–42. http://dx.doi.org/10.1366/0003702864508782.

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Carbon13 chemical shift assignments are reported for Z- and E-doxepin hydrochloride [ Z- and E-N,N,-dimethyl-dibenz[b,e]oxepin-delta-11(6H)], gamma-propylamine hydrochloride, and related model compounds. Doxepin hydrochloride, a mixture of approximately 85% E- and 15% Z-isomer is of clinical importance as an antidepressant drug. Previous proton NMR studies indicated that the dibenz(b,e,)oxepin ring exists in two conformations. This study indicates that one conformation may be favored for each isomer with alkylamino olefinic substituent orientation above the most adjacent aromatic ring. Homoand

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8

Minassian, Frédéric, Nadia Pelloux-Léon, Marie-Thérèse Averbuch-Pouchot, and Yannick Vallée. "Rearrangements in the 11-Thia-9,10-dihydro-9,10-ethanoanthracene Series. Synthesis of a Bridged Thienooxepin." Journal of Chemical Research 23, no. 2 (1999): 166–67. http://dx.doi.org/10.1177/174751989902300250.

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9

KLOTZ, B., I. BARNES, K. H. BECKER, and B. T. GOLDING. "ChemInform Abstract: Atmospheric Chemistry of Benzene Oxide/Oxepin." ChemInform 28, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.199728205.

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10

Hou, Yan-Jun, Shu-Lin Song, Wen-Yi Chu, and Zhi-Zhong Sun. "2,9,10-Trimethoxydibenzo[b,d]oxepin-7(6H)-one." Acta Crystallographica Section E Structure Reports Online 68, no. 1 (2011): o204. http://dx.doi.org/10.1107/s1600536811053803.

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Dissertations / Theses on the topic "Oxepin"

1

Gantert, Carla [Verfasser], and Michael [Akademischer Betreuer] Müller. "Untersuchungen zur biokatalytischen Reduktion alpha,beta-ungesättigter Carbonylverbindungen, Die hydrolytische Oxepin-CoA-Ringspaltung des aeroben Phenylessigsäure-Stoffwechsels." Freiburg : Universität, 2012. http://d-nb.info/1123466610/34.

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2

Doveston, Richard Gerard. "Oxepine-pyrimidinone natural products : the total synthesis of (±)-janoxepin." Thesis, University of York, 2012. http://etheses.whiterose.ac.uk/2397/.

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The first total synthesis of (±)-janoxepin I, an antiplasmodial oxepine-pyrimidinone natural product isolated from the fungus Aspergillus janus is described herein. Chapter 1 provides an introduction to janoxepin I and related natural products that have been reported in the literature. In Chapter 2, the available methods for the synthesis of oxepines and pyrimidinones are reviewed, before the preparation of dihydro-oxepine VI from readily available starting materials II-V is described. The enamine side-chain seen in janoxepin I was introduced by way of aldol-addition to the ketopiperazine ring

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Leyhane, Andrew John. "Cyclobutadiene cycloadditions : applications toward the synthesis of functionalized oxepines and guaiane natural products." Thesis, Boston College, 2008. http://hdl.handle.net/2345/1360.

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Xia, Shijing. "Experimental and Computational Studies for Various Organic Systems." The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1204309077.

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5

Cebon, Benjamin Isaiah Martin. "Studies towards the biomimetic total synthesis of dihydrooxepin-containing epipolythiodiketopiperazine natural products." Connect to thesis, 2009. http://repository.unimelb.edu.au/10187/8526.

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SCH-64874 (5) is a fungal metabolite that inhibits the epidermal growth factor receptor (EGFR), a high-profile oncology target, with an IC50 of 1.0µg/mL. It is of particular interest because it is unlikely to inhibit the protein’s intramolecular kinase domain (as typical chemical EGFR inhibitors do), and may act instead by obstructing the receptor’s ligand binding and/or dimerisation processes.<br>In this work, the epipolythiodiketopiperazine family of natural products is reviewed, leading to a discussion of the probable biosynthetic pathways by which these complex molecules are produced in na

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6

Gallant, Pascal. "Synthesis of oxepane nucleosides by ring expansion and ring closing routes." Thesis, McGill University, 2011. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103473.

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Modified nucleosides form an important class of antiviral and anticancer agents, and nucleic acids bearing modified nucleosides hold great promise as therapeutic agents. Oxepane nucleosides and nucleic acids are members of this important class of compounds. Oxepane nucleosides have a seven-membered carbohydrate ring instead of the canonical five-membered pentafuranose ring. This thesis describes work in the development of new synthetic approaches and routes in the synthesis of oxepane nucleosides. In chapter 2, the synthesis of oxepane nucleosides based on the ring expansion approach is descri

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Zhang, Wei. "Total synthesis of biologically relevant natural products in the diketopiperazine and oxepine series : oxidative functionalizations and oxa-Cope rearrangement studies." Thesis, Sorbonne université, 2018. http://www.theses.fr/2018SORUS433.

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La synthèse biomimétique, inspirée par des voies de biosynthèse directes et rapides, est un moyen efficace pour produire des produits complexes. Le travail de cette thèse a porté sur le développement de stratégies collectives à partir d’intermédiaires biomimétiques pour accéder rapidement à trois familles de dikétopipérazines : les gliocladrides (DKPs fonctionnalisés), les quinazolino-DKPs et les oxépino-DKPs. Les fonctionnalisations oxydantes tardives par voies chimiques et biologiques des deux premiers intermédiaires ont été envisagées dans le but d’accéder directement au gliocladride A et a

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8

Kassir, Ahmad. "Photochemical approaches for the synthesis of oxygen- and sulphur-containing heterocycles." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS065.

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Les oxétanes sont des cycles à quatre chaînons comportant un atome d’oxygène intracyclique. Le motif oxétane est présent dans la structure de nombreux produits naturels et dans un large panel de composés de synthèse pour la recherche pharmaceutique. Les thiétanes sont des cycles à quatre chaînons comportant un atome de soufre intracyclique. Le motif thiétane, est quant à lui moins répandu au sein de molécules bioactives et il n’existe à ce jour qu’un nombre restreint d’études le concernant. Ils sont tous deux prisés également comme intermédiaires de synthèse du fait de la grande réactivité int

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9

Monto, Alexander V. "Six months like oxen, six months like kings : circulatory migration from Mexico." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239490.

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10

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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Books on the topic "Oxepin"

1

Musk-oxen. Child's World, 1991.

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2

Black oxen. Chatto & Windus, 2001.

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Owen, Ruth. Musk oxen. Windmill Books, 2013.

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Knox, Elizabeth. Black oxen. Victoria University Press, 2001.

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Musk oxen. Gareth Stevens Pub., 2011.

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Black oxen. Farrar, Straus and Giroux, 2001.

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Musk oxen. Lerner Publications Company, 2007.

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8

Conroy, Drew. The oxen handbook. D. Butler, 1986.

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9

Halstead, Paul. Two Oxen Ahead. John Wiley & Sons, Ltd., 2014. http://dx.doi.org/10.1002/9781118819333.

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10

Sadler, Genevieve Grant. Muzzled oxen: A memoir. Sooner or Later, 2013.

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Book chapters on the topic "Oxepin"

1

Rosowsky, Andre. "Oxepin Ring Systems Containing Two Rings." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186961.ch2.

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2

Rosowsky, Andre. "Oxepin Ring Systems Containing Three Rings." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186961.ch3.

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3

Rosowsky, Andre. "Oxepin Ring Systems Containing More Than Three Rings." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186961.ch4.

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4

Rosowsky, Andre. "Oxepins and Reduced Oxepins." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186961.ch1.

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5

Atta-ur-Rahman and Viqar Uddin Ahmad. "Oxepine." In 13C-NMR of Natural Products. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3290-3_75.

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6

Starratt, A. N. "Terpene Oxepins." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186961.ch6.

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7

Zderic, John A. "Steroidal Oxepins." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186961.ch7.

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8

Ghiron, Chiara, and Russell J. Thomas. "Synthese von (±)-Oxerin." In Teubner Studienbücher Chemie. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-80121-0_20.

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9

Boyd, Derek R., and Donald M. Jerina. "Arene Oxides-Oxepins." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187203.ch2.

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Atta-ur-Rahman and Viqar Uddin Ahmad. "Oxepane." In 13C-NMR of Natural Products. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3288-0_3.

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Conference papers on the topic "Oxepin"

1

Gerbino, Darío, Jimena Scoccia, M. Julia Castro, M. Belén Faraoni, Cecilia Bouzat, and Víctor S. Martín. "Efficient synthesis and biological evaluation of dibenzo[b,e]oxepin-11(6H)-ones as potential anthelmintic agents." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a021.

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2

Shaw, R. A., N. Ibrahim, L. A. Nafie, A. Rauk, and H. Wieser. "The VCD Spectrum Of 2-Methyl Oxetan." In 1985 International Conference on Fourier and Computerized Infrared Spectroscopy, edited by David G. Cameron and Jeannette G. Grasselli. SPIE, 1985. http://dx.doi.org/10.1117/12.970899.

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Xu, TianXiang, Xiao Leng, Shuangping Huang, and Xiaoji Wang. "Study on Synthesis Of Oxetan-3-ol." In 2015 2nd International Conference on Machinery, Materials Engineering, Chemical Engineering and Biotechnology. Atlantis Press, 2016. http://dx.doi.org/10.2991/mmeceb-15.2016.163.

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McKenzie, Grant, Benjamin Adams, and Krzysztof Janowicz. "Of Oxen and Birds." In SIGSPATIAL'15: 23rd SIGSPATIAL International Conference on Advances in Geographic Information Systems. ACM, 2015. http://dx.doi.org/10.1145/2830657.2830659.

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Gharaibeh, Abdullah, Lauro Beltrão Costa, Elizeu Santos-Neto, and Matei Ripeanu. "A yoke of oxen and a thousand chickens for heavy lifting graph processing." In the 21st international conference. ACM Press, 2012. http://dx.doi.org/10.1145/2370816.2370866.

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Feng-Ying Dong, Yun-Ming Sun, Yan-Li Wang, Cai-Zhen Ding, and Wen-Hua Yin. "Synthesis and crystal structure of a novel sheet-like heteronuclear complex, [Cu2(oxen)Fe(CN)5(NO)]n, H2oxen = N,N'-bis(2-aminoethyl)oxamide." In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5966284.

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Reports on the topic "Oxepin"

1

P., BASTIAENSEN. Triage in the trenches, for the love of animals : a tribute to veterinarians in the First World War. O.I.E (World Organisation for Animal Health), 2018. http://dx.doi.org/10.20506/bull.2018.nf.2883.

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On the occasion of the centenary of the First World War, remembered across the world from 2014 until the end of 2018, many aspects and experiences of this global conflict have been re-examined or brought to light for the first time, as we honour the memory of those estimated 16 million soldiers and civilians who perished in what was then known as the ‘Great War’, or the ‘War to End All Wars’. So many of these died on the infamous fields of Flanders, where Allied and Central Forces dug themselves into trenches for the better part of four years. Over the past few years, new research has brought

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