Academic literature on the topic 'Benzotriazine'

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Journal articles on the topic "Benzotriazine"

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Cui, Bingcun, Guosheng Huang, Jin Liu, et al. "Palladium-Catalyzed ortho-Monoacylation of Arenes with Aldehydes­ via 1,2,4-Benzotriazine-Directed C–H Bond Activation." Synthesis 52, no. 09 (2020): 1407–16. http://dx.doi.org/10.1055/s-0039-1691564.

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An efficient palladium-catalyzed C–H bond functionalization/ortho-monoacylation reaction of 3-aryl-1,2,4-benzotriazines with (hetero)aryl or alkyl aldehydes has been developed, which offers a facile and alternative strategy for direct modification and further diversification of 3-aryl-1,2,4-benzotriazines. Bioactive 1,2,4-benzotriazine has been employed as a novel directing group for the palladium-catalyzed regioselective monoacylation of sp2 C–H bond protocol with broad substrate scope and good functional group tolerance.
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Werstiuk, Nick Henry, Chandra Deo Roy, and Jiangong Ma. "A study of the vacuum pyrolysis of 1,2,3-benzotriazines. The Hel ultraviolet photoelectron spectra of benzazete and o-benzyne." Canadian Journal of Chemistry 73, no. 1 (1995): 146–49. http://dx.doi.org/10.1139/v95-022.

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A CW CO2 laser is used as a directed heat source to carry out the vacuum pyrolysis of 1,2,3-benzo-triazine (1a) and 4-methyl-1,2,3-benzotriazine (1b). We report the first HeI photoelectron (pe) spectrum of benzazete (2a), which correlates with ionization energies calculated with HAM/3 using an equilibrium geometry obtained at the ab initio HF/6-31G** level of the theory. The pe spectrum of o-benzyne (3) obtained in this study correlates with the spectrum published by Zhang and Chen, but not with the spectra reported in two earlier publications. Keywords: 1,2,3-benzotriazines, vacuum pyrolysis,
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Cortés, Edwar, Rodrigo Abonía, Justo Cobo, and Christopher Glidewell. "Four related esters: two 4-(aroylhydrazinyl)-3-nitrobenzoates and two 3-aryl-1,2,4-benzotriazine-6-carboxylates." Acta Crystallographica Section C Crystal Structure Communications 69, no. 7 (2013): 754–60. http://dx.doi.org/10.1107/s0108270113013590.

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The molecules of both methyl 4-[2-(4-chlorobenzoyl)hydrazinyl]-3-nitrobenzoate, C15H12ClN3O5, (I), and methyl 4-[2-(2-fluorobenzoyl)hydrazinyl]-3-nitrobenzoate, C15H12FN3O5, (II), contain an intramolecular N—H...O hydrogen bond, and both show electronic polarization in the nitrated aryl ring. In both compounds, molecules are linked by a combination of N—H...O and C—H...O hydrogen bonds to form sheets, which are built fromR43(18) rings in (I) and fromR44(28) rings in (II). In each of methyl 3-phenyl-1,2,4-benzotriazine-6-carboxylate, C15H11N3O2, (III), and methyl 3-(4-methylphenyl)-1,2,4-benzot
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Boulton, A. J., Mikl�s Kiss, and J. D. Kalenga Saka. "1,2,3-Benzotriazine 2-oxides." Journal of the Chemical Society, Perkin Transactions 1, no. 6 (1988): 1509. http://dx.doi.org/10.1039/p19880001509.

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Sparatore, Fabio, and Anna Sparatore. "3,3-Disubstituted 3,4-Dihydro-1,2,4-benzotriazines: Chemistry, Biological Activity, and Affinity to Sigma Receptors." Molecules 29, no. 1 (2023): 132. http://dx.doi.org/10.3390/molecules29010132.

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By reducing the 2-nitrophenylhydrazone of cyclohexanone with sodium dithionite, an unexpected yellow compound was obtained instead of the corresponding colorless amino derivative. Many years later, the structure of this compound, namely, cyclohexane-3-spiro-3,4-dihydro-1,2,4-benzotriazine, was demonstrated. From that time, the reduction of 2-nitrophenylhydrazones of different kinds of ketones, followed by air oxidation of the initially formed amino compounds, has represented a general way to synthesize a variety of 3,3-disubstituted 3,4-dihydro-1,2,4-benzotriazines. Many derivatives have been
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Elsaidi, Hassan, Fatemeh Ahmadi, Leonard Wiebe, and Piyush Kumar. "Development of [131I]I-EOE-TPZ and [131I]I-EOE-TPZMO: Novel Tirapazamine (TPZ)-Based Radioiodinated Pharmaceuticals for Application in Theranostic Management of Hypoxia." Pharmaceuticals 12, no. 1 (2019): 3. http://dx.doi.org/10.3390/ph12010003.

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Introduction: Benzotriazine-1,4-dioxides (BTDOs) such as tirapazamine (TPZ) and its derivatives act as radiosensitizers of hypoxic tissues. The benzotriazine-1-monoxide (BTMO) metabolite (SR 4317, TPZMO) of TPZ also has radiosensitizing properties, and via unknown mechanisms, is a potent enhancer of the radiosensitizing effects of TPZ. Unlike their 2-nitroimidazole radiosensitizer counterparts, radiolabeled benzotriazine oxides have not been used as radiopharmaceuticals for diagnostic imaging or molecular radiotherapy (MRT) of hypoxia. The radioiodination chemistry for preparing model radioiod
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Heravi, M. M., K. Aghapoor, M. A. Nooshabadi, and M. M. Mojtahedi. "Regioselective annelation of 3-(prop-2-ynylsulfanyl)-1,2,4-benzotriazine to thiazolo[2,3-c][1,2,4]benzotriazine." Monatshefte für Chemie - Chemical Monthly 128, no. 11 (1997): 1143–47. http://dx.doi.org/10.1007/bf00807564.

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Nicoló, F., M. Panzalorto, R. Scopelliti, G. Grassi, and F. Risitano. "5,7-Dimethyl-3-phenyl-1,2,4-benzotriazine." Acta Crystallographica Section C Crystal Structure Communications 54, no. 3 (1998): 405–7. http://dx.doi.org/10.1107/s0108270197014972.

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Shinde, Sujata S., Robert F. Anderson, Michael P. Hay, Swarna A. Gamage, and William A. Denny. "Oxidation of 2-Deoxyribose by Benzotriazinyl Radicals of Antitumor 3-Amino-1,2,4-benzotriazine 1,4-Dioxides." Journal of the American Chemical Society 126, no. 25 (2004): 7865–74. http://dx.doi.org/10.1021/ja048740l.

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HERAVI, M. M., K. AGHAPOOR, M. A. NOOSHABADI, and M. M. MOJTAHEDI. "ChemInform Abstract: Regioselective Annelation of 3-(Prop-2-ynylsulfanyl)-1,2,4-benzotriazine to Thiazolo[2,3-c][1,2,4]benzotriazine." ChemInform 29, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.199811176.

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Dissertations / Theses on the topic "Benzotriazine"

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Virk, Narinder Singh. "DNA damaging effects of benzotriazine-N-oxides." Thesis, University of East London, 1993. http://roar.uel.ac.uk/3605/.

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The aim of this study was to investigate the DNA damaging abilities of SR 4233 (Tirapazamine) and a range of congeners. These are novel benzotriazine-N-oxide compounds of potential clinical importance in the treatment of hypoxic tumours. The studies used a viral double transfection assay which involved exposing purified $X174 DNA to the compounds under oxic, hypoxic and hypoxic reductive conditions and subsequently transfecting the DNA into E. coli AB1157 and E. coli C. Experiments under reductive hypoxia were carried out between pH 4-7 to establish if a reduction product required protonation
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Walmsley, Ray. "Effects of the benzotriazine-di-N-oxide tirapazamine upon DNA." Thesis, University of East London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361475.

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Nakhai, Azadeh. "Synthetic studies of nitrogen containing heterocycles, particularly pyrazole and benzotriazine derivatives." Stockholm, 2009. http://diss.kib.ki.se/2009/978-91-7409-687-3/.

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McCandless, Stewart Grant. "The synthesis of some novel 1,2,3-benzotriazine-platinum complexes with potential antineoplastic activity." Thesis, Heriot-Watt University, 1988. http://hdl.handle.net/10399/999.

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Daniels, John Scott. "Investigations into the mechanism of DNA cleavage activity by the reductively-activated antitumor agent 3-amino-1,2,4-benzotriazine 1,4 dioxide and related heterocyclic N-oxides /." free to MU campus, to others for purchase, 1998. http://wwwlib.umi.com/cr/mo/fullcit?p9901232.

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Yang, Hongfang. "Benzotriazole intermediates in organic chemistry." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0005743.

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Yoshioka-Tarver, Megumi. "Benzotriazole intermediates for heterocycles and pharmaceuticals." [Gainesville, Fla.] : University of Florida, 2009. http://purl.fcla.edu/fcla/etd/UFE0041025.

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Wood, Paul Michael. "Novel aspects of the photochemistry of benzotriazole." Thesis, University of Bristol, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288297.

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Plützer, Christian. "Doppelresonanzspektroskopie an biologisch relevanten Systemen." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=96637813X.

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Rollinson, G. "'Benzotriazole biodegradation' and 'The production of thiacetazone using microorganisms'." Thesis, Bucks New University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373796.

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Books on the topic "Benzotriazine"

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Virk, Narinder Singh. DNA damaging effects of benzotriazine-N-oxides. University of East London, 1993.

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Walmsley, Ray. Effects of the benzotriazine-di-n-oxide tirapazamine upon dna. UEL, 1995.

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Monbaliu, Jean-Christophe M., ed. The Chemistry of Benzotriazole Derivatives. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31554-6.

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Hughes, Craig V. Preparation and synthetic transformations of benzotriazole derivatives. 1989.

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Maimait, Rexiat. Some Synthetic Applications of Benzotriazole Methodology. Creative Media Partners, LLC, 2019.

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Jiang, Jinlong. Benzotriazole-phosphorus reagents in organic synthesis. 1993.

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Maimait, Rexiat. Some synthetic applications of benzotriazole methodology. 2002.

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Maimait, Rexiat. Some Synthetic Applications of Benzotriazole Methodology. Dissertation Discovery Company, 2019.

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Cheng, Dai. Some examples of benzotriazole-mediated sythesis. 1997.

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Nichols, Daniel A. Synthesis and utility of some N-substituted benzotriazoles. 1999.

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Book chapters on the topic "Benzotriazine"

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Edwards, D. I., J. H. Tocher, L. D. Dale, D. Widdick, and N. Virk. "Effects on DNA of Bioreducible Nitroimidazole and Benzotriazine Drugs." In Selective Activation of Drugs by Redox Processes. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3768-7_25.

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Brown, J. Martin. "Redox Activation of Benzotriazine N-Oxides: Mechanisms and Potential as Anticancer Drugs." In Selective Activation of Drugs by Redox Processes. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3768-7_12.

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Bährle-Rapp, Marina. "Benzotriazole." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1090.

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Gooch, Jan W. "Benzotriazole." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1227.

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Whelligan, Daniel K. "Benzotriazole Linker Units." In Linker Strategies in Solid-Phase Organic Synthesis. John Wiley & Sons, Ltd, 2009. http://dx.doi.org/10.1002/9780470749043.ch11.

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Meldal, Morten, and Robert C. Sheppard. "ESTERS OF FMOC-AMINO ACIDS WITH 3,4,-DIHYDRO-3-HYDROXY-4-OXO-1,2,3-BENZOTRIAZINE. A NEW CLASS OF SELF-INDICATING, ACTIVATED INTERMEDIATES FOR SOLID PHASE SYNTHESIS." In Porto Carras, Chalkidiki, Greece, Aug. 31–Sept. 5, 1986, edited by Dimitrios Theodoropoulos. De Gruyter, 1987. http://dx.doi.org/10.1515/9783110864243-027.

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van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "2-(2-Hydroxy-5-methylphenyl)benzotriazole." In Spectra for the Identification of Additives in Food Packaging. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_48.

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Gooch, Jan W. "2(2′-Hydroxy-4′-Methylphenyl) Benzotriazole." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6166.

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Beagle, Judit K. "Benzotriazole-Mediated Synthesis of Nitrogen-Containing Heterocycles." In Topics in Heterocyclic Chemistry. Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_178.

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Bolshakov, Oleg I. "Benzotriazole-Mediated Synthesis of Oxygen-Containing Heterocycles." In Topics in Heterocyclic Chemistry. Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_180.

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Conference papers on the topic "Benzotriazine"

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Akyüz, Mehmet Ali, and Asuman Celepçi Ergan. "Behaviour of Benzotriazole Salts in Multi Metal Formulations for Corrosion Inhibition of Copper." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-3962.

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Abstract Benzotriazole and triazole compounds are well-known copper corrosion inhibitors. Also benzotriazole is used as Vapor Corrosion Inhibitor (VCIs) for copper. Sometimes copper is used together with iron and other metals within the same part or structure. To protect mixed metal components that have copper, benzotriazole is used along with other corrosion inhibitors as in multi-metal inhibitor formulations. However, when mixed with other corrosion inhibitors the chemicals may react with benzotriazole and may generate different kinds of salts. These new salts may cause more harm to copper.
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Frail, Paul R., Martin M. Morra, and Gilad Zorn. "Performance Analysis of Commercial Azoles for Yellow Metal Corrosion Control Utilizing Surface Analysis and Electrochemistry." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-4246.

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Abstract Commercial azoles benzotriazole (BZT), tolyltriazole (TTA), and butyl benzotriazole (BBZT) are well known water industrial yellow metal corrosion inhibitors. BZT, TTA, and BBZT are all organic film forming species that coordinate and passivate the surface providing protection from corrosive species such as chloride and sulfates, which have been reported to be due to the stabilization of Cu(I), and providing a hydrophobic barrier on the surface. In this study the performances of BZT, TTA, and BBZT are analyzed based on their bulk corrosion properties, mpy (mills per year) and electrode
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May, Roger C., Longchun Cheng, and Feng Shao. "Second Generation, Halogen Resistant Copper Corrosion Inhibitors." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02413.

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Abstract Copper alloys are utilized in industrial cooling systems because of their excellent heat transfer properties. However, a corrosion inhibitor is needed to prevent equipment failures and, very importantly, to reduce the discharge of toxic copper compounds into the environment. Azoles, such as benzotriazole (BZT) and tolyltriazole (TTA), have been used for this purpose but they do not protect copper in the presence of oxidizing halogens which are commonly added to cooling systems to control microbiological activity. The halogens react with BZT and TTA and destroy their corrosion inhibiti
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Frail, Paul R., Edward J. Urankar, Gilad Zorn, and Martin M. Morra. "New Yellow Metal Corrosion Inhibitors Targeting Surface Chemistry of Industrial Systems." In CORROSION 2017. NACE International, 2017. https://doi.org/10.5006/c2017-09719.

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Abstract Phosphate is the most common inhibitor used in industrial waters for iron surfaces. When phosphate combines with calcium, calcium phosphate colloids form in solution, and then form a cathodic passivation film on top of the iron oxide layer. Surface analysis was used to examine chemical composition and the formation process of the passivation film. It was found that the dispersant polymer used to control scale inhibition plays a significant role in the calcium phosphate passivation mechanism for iron surfaces. Azoles have long been used in industry to protect yellow metal surfaces and
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Pujar, Mohan, Albert E. Miller, Kunigahalli L. Vasanth, and Gautam Banerjee. "Some Investigations on the Monocarboxylic Acid Based Inhibitors for Aluminum Alloys." In CORROSION 2000. NACE International, 2000. https://doi.org/10.5006/c2000-00331.

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Abstract This paper deals with the electrochemical investigations on three (Capric, Lauric and Myristic acids) different long chain carboxylic acids as inhibitors that were studied in a solution of water and an alcohol at pH of 8.4 - 8.5. The Electrochemical Impedance Spectroscopic (EIS) and potentiodynamic anodic polarization experiments were conducted on Al 2024 and Al 6061 specimens in the solutions containing these inhibitors to determine the effectiveness of these inhibitors. Among the three acids, Lauric acid was found to be the most effective in inhibiting the uniform and localized corr
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Raman, A. "Temperature Effects on Inhibitors and Corrosion Inhibition." In CORROSION 1996. NACE International, 1996. https://doi.org/10.5006/c1996-96216.

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Abstract Inhibitor systems commonly employed in industrial operations at elevated and high temperatures are surveyed and the available literature data on their performance characteristics at elevated temperatures are analyzed. The functional behavior of phosphates, amines, benzotriazole, and other important inhibitors are briefly summarized. The inhibitors degrade due to thermal decomposition and/or reaction on the metal surface or with other species present in the environment. Degradation modes of various kinds of amines used in steam systems are reviewed and the resultant limitations for use
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Ellor, J. A., G. A. Gehring, and Barry C. Syrett. "An Investigation of Water Treatments for Mitigating Sulfide-Related Corrosion of Copper Alloy Condenser Tubes." In CORROSION 1986. NACE International, 1986. https://doi.org/10.5006/c1986-86225.

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Abstract This paper presents the results of a study investigating selected water treatments that might be used to control sulfide-accelerated corrosion. The water treatments selected for evaluation included ferrous sulfate, benzotriazole, sodium dimethyl-dithiocarbamate, high molecular weight polyacrylamide, and Calgon CL-5. The study also evaluated the interaction and effect of sulfide, dissolved oxygen and temperature on the corrosion of copper alloy tubes under simulated condenser flow conditions. The program included three condenser tube alloys--aluminum brass, 70/30 copper-nickel, and 90/
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Ahn, M. H., and K. K. Baek. "Evaluation of Combined Effect of Organic and Inorganic Inhibitors on the Metals Used in Absorption Refrigeration System." In CORROSION 1999. NACE International, 1999. https://doi.org/10.5006/c1999-99097.

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Abstract To develop "environment-friendly" inhibitors for the metals used in the absorption refrigeration system, inhibition efficiencies of six different combinations of inhibitors were evaluated in 64wt.%LiBr solution at 160°C. Double and triple combinations of inhibitors, such as lithium molydate (Li2MoO4 inorganic), lithium hydroxide (LiOH, inorganic), and benzotriazole (BTA, organic) were evaluated for their efficiencies in corrosion inhibition of copper and mild steel. Results from weight-loss tests showed that the double inhibitor combinations were less effective for copper than for mil
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Santos, Bill, Mohammed Kashanian, and Chris Friesen. "Optimization of Cooling Water System Passivation of Brass Alloys in Petrochemical Facilities." In CORROSION 2010. NACE International, 2010. https://doi.org/10.5006/c2010-10050.

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Abstract In order to optimize a corporate cooling water program, real-world plant experience along with a series of laboratory experimental studies is being used. All aspects of the program are being considered, including passivation treatments for individual bundles, system pre-film solutions, and long-term cooling water chemistries. The aim of the optimization plan is to select the most favorable combination of passivation, pre-film, and cooling water solutions that provides the most cost-effective protection of the system within defined performance targets that the vendor must deliver. This
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Chen, Yu-Sen, and Tzu-Yu Chen. "Mechanistic Studies of Copper Corrosion and Corrosion Inhibition under Simulated Boiler Conditions." In CORROSION 1991. NACE International, 1991. https://doi.org/10.5006/c1991-91147.

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Abstract The effect of pH, dissolved oxygen concentration, ammonia, and morpholine on potentiodynamic polarization curves of copper were investigated under simulated condensate conditions at 80°C and 500 rpm with a rotating cylinder electrode. At pH 9, a passive region was observed in the anodic curve. This was believed to result from the formation of the Cu2O/CuOH film. At pH 7, the passive region disappeared. At pH 11, an active-passive transition peak occurred indicating that the film formation became more difficult. However, better passivation was possible at pH 11 in strongly oxidizing en
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Reports on the topic "Benzotriazine"

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Lu, Q., and J. H. Boyer. Luminescent Nitro Derivatives of Benzotriazolo(2,1-a)Benzotriazole. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada251183.

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Zonnevylle, M. C., and R. Hoffmann. The Absorption of Benzotriazole on Copper and Cuprous Oxide. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada198958.

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Obrien, Ivette Z. Biotransformation Potential and Uncoupling Behavior of Common Benzotriazole-Based Corrosion Inhibitors. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada414450.

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