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Relevant bibliographies by topics / Azidy

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Academic literature on the topic 'Azidy'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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Journal articles on the topic "Azidy"

1

Dong, Z., KA Hellmund та SG Pyne. "Chiral Sulfur Compounds. XXI. Addition of Azide Ion to β-Aryl-α-phenylsulfinylacrylates". Australian Journal of Chemistry 46, № 9 (1993): 1431. http://dx.doi.org/10.1071/ch9931431.

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The reaction of methyl β-aryl-α- phenylsulfinylacrylates (1) with sodium azide /acetic acid gives triazoles (6) while the reaction of (1) with sodium azide /hydrochloric acid gives β-azido esters (7a,b). Reaction of (7a) with 1,8-diazabicyclo[5.4.0]undec-7-ene, and (7b) with triethylamine gave the corresponding triazoles (6a) and (6b), respectively. Thus the formation of triazoles from the reaction of acrylates with azide ion most likely involves Michael addition of azide ion followed by cyclization of an incipient β-azido α-anion.

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2

Yang, Tonghao, Haizhen Zhu, and Wei Yu. "Copper-catalyzed radical reactions of 2-azido-N-arylacrylamides with 1-(trifluoromethyl)-1,2-benziodoxole and 1-azidyl-1,2-benziodoxole." Organic & Biomolecular Chemistry 14, no. 13 (2016): 3376–84. http://dx.doi.org/10.1039/c6ob00226a.

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The tandem addition/cyclization reactions of 2-azido-N-arylacrylamides with 1-(trifluoromethyl)-1,2-benziodoxole and 1-azidyl-1,2-benziodoxole-derived trifluoromethyl radicals and azidyl radicals were investigated.

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3

Zhao, Jiong-Peng, Cui Zhao, Wei-Chao Song, et al. "4-Substituent pyridine directed cobalt(ii) azides: solvothermal synthesis, structure, and magnetic properties." Dalton Transactions 44, no. 22 (2015): 10289–96. http://dx.doi.org/10.1039/c5dt00568j.

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Azido-bridged magnetic complexes: Different 4-substituent groups of pyridine co-ligands directed the linkages between azide and Co(ii) ions, to give three azide–Co(ii) complexes with different structures and magnetic properties.

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4

Forman, Grant S., Adrian Scaffidi та Robert V. Stick. "An Alternative Synthesis of Some Carbohydrate α-Amino Acids". Australian Journal of Chemistry 57, № 1 (2004): 25. http://dx.doi.org/10.1071/ch03214.

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Several carbohydrate ketones have been converted into their trichloromethyl-branched tertiary alcohols. A subsequent treatment of these alcohols under Corey–Link conditions (base, sodium azide, methanol) has given rise to α-azido esters, transformable into azido acids, amino esters, and amino acids. An amino ester and an azido acid have been coupled to form a dipeptide.

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5

Stamatatos, Theocharis C., and Eva Rentschler. "Organic chelate-free and azido-rich metal clusters and coordination polymers from the use of Me3SiN3: a new synthetic route to complexes with beautiful structures and diverse magnetic properties." Chemical Communications 55, no. 1 (2019): 11–26. http://dx.doi.org/10.1039/c8cc08854c.

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A new synthetic route to structurally novel and magnetically interesting 3d-metal azido clusters and coordination polymers is presented; the key reagent for the preparation of solely azido-bridged molecule-based species is the organic azide precursor Me<sub>3</sub>SiN<sub>3</sub>.

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6

Goher, Mohamed A. S., and Franz A. Mautner. "Preparation, Spectral and Structural Characterization of Two Polymeric 1:1 Mixed Ligand Complexes of Copper(II) Azide with 4-Methylquinoline and 2-Methylpyridine." Zeitschrift für Naturforschung B 46, no. 5 (1991): 687–92. http://dx.doi.org/10.1515/znb-1991-0522.

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Two 1:1 mixed ligand complexes of copper(II) azide with substituted quinoline and pyridine, namely catena di-μ(1,1)-azido-(4-methylquinoline)copper(II) (1) and catena di-μ(1,3)-azido-[di-μ(1,1)-azido-bis(2-methylpyridine)dicopper(II)] (2) have been prepared and characterized by X-ray crystallography.Crystal data: 1, C10H9N7Cu, space group P21/c, a = 577.8(2), b = 2202.3(5), c = 919.9(2) pm, β = 93.92(2)°, Ζ = 4, and R = 0.035 for 1293 observed MoKa data; 2, C6H7N7Cu, space group P21/a, a = 823.7(2), b = 1303.8(4), c = 895.3(3) pm, β = 112.23(2)°, Ζ = 4, and R = 0.022 for 2133 observed ΜοΚα dif

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7

Resende, Diana I. S. P., Amalia M. Estévez, Andre M. Alker, Rainer E. Martin, and Hans Peter Wessel. "A carbohydrate-derived trifunctional scaffold for medicinal chemistry library synthesis." Mediterranean Journal of Chemistry 7, no. 2 (2018): 135–44. http://dx.doi.org/10.13171/mjc72/01809051415-wessel.

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For the generation of compound libraries for drug discovery a central scaffold containing three exit vectors with defined chirality was devised starting from commercially available tri-O-acetyl-glucal. Surprisingly, the reaction of a 4-O-mesylate with sodium azide did not lead to the expected 4-azido-4-deoxy derivative but to a 3-azido-3-deoxy regioisomer via intermediate epoxide formation. The absolute stereochemical configuration of the final tetrahydropyran building block was proven by X-ray crystallography. This scaffold endowed with a carboxylic acid, a secondary alcohol, and an azide fun

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8

Kumar, Rakesh, Leonard I. Wiebe, and Edward E. Knaus. "A mild and efficient methodology for the synthesis of 5-halogeno uracil nucleosides that occurs via a 5-halogeno-6-azido-5,6-dihydro intermediate." Canadian Journal of Chemistry 72, no. 9 (1994): 2005–10. http://dx.doi.org/10.1139/v94-256.

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A mild and efficient methodology for the synthesis of 5-halogeno (iodo, bromo, or chloro) uracil nucleosides has been developed. 5-Halo-2′-deoxyuridines 4a–c (84–95%), 5-halouridines 7a–c (45–95%), and 5-haloarabinouridines 8a–c (65–95%) were synthesized in good to excellent yields by the reaction of 2′-deoxyuridine (2), uridine (5), and arabinouridine (6), respectively, with iodine monochloride, or N-bromo (or chloro)succinimide, and sodium azide at 25–45 °C. These C-5 halogenation reactions proceed via a 5-halo-6-azido-5,6-dihydro intermediate (3), from which HN3 is eliminated, to yield the

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9

Ge, Junying, Qiuping Ding, Man Yang, Tian He, and Yiyuan Peng. "Copper and manganese co-mediated cascade aza-Michael addition/cyclization and azidation of 1,3-enynes: regioselective synthesis of fully substituted azido pyrroles." Organic & Biomolecular Chemistry 18, no. 43 (2020): 8908–15. http://dx.doi.org/10.1039/d0ob01927e.

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10

Hema, Kuntrapakam, and Kana M. Sureshan. "Three-way competition in a topochemical reaction: permutative azide–alkyne cycloaddition reactions leading to a vast library of products in the crystal." CrystEngComm 20, no. 11 (2018): 1478–82. http://dx.doi.org/10.1039/c8ce00131f.

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Dissertations / Theses on the topic "Azidy"

1

Merkel, Roswitha. "Untersuchung zur Synthese und Eigenschaften von komplexen Oligospiroketalen." Phd thesis, Universität Potsdam, 2014. http://opus.kobv.de/ubp/volltexte/2015/7256/.

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Es ist in dieser Arbeit gelungen, starre Oligospiroketal(OSK)-Stäbe als Grundbausteine für komplexe 2D- und 3D-Systeme zu verwenden. Dazu wurde ein difunktionalisierter starrer Stab synthetisiert, der mit seines Gleichen und anderen verzweigten Funktionalisierungseinheiten in Azid-Alkin-Klickreaktionen eingesetzt wurde. An zwei über Klickreaktion verknüpften OSK-Stäben konnten mittels theoretischer Berechnungen Aussagen über die neuartige Bimodalität der Konformation getroffen werden. Es wurde dafür der Begriff Gelenkstab eingeführt, da die Moleküle um ein Gelenk gedreht sowohl gestreckt als a

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2

Okumu, Antony A. "Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide." Youngstown State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290962115.

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3

Mackay, Fiona S. "Photoactive platinum azide anticancer complexes." Thesis, University of Edinburgh, 2006. http://hdl.handle.net/1842/11085.

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Photoactive platinum compounds have the potential to reduce some of the debilitating side-effects associated with conventional chemotherapeutics, such as cisplatin. Stable, inert platinum(IV) compounds which are reduced to active platinum(II) species only upon irradiation, could provide a site-specific treatment. The Pt<sup>IV</sup> azide complexes, <i>cis, trans, cis-</i>[Pt(N<sub>3</sub>)<sub>2</sub>(OH)<sub>2</sub>(NH<sub>3</sub>)<sub>2</sub>] and <i>cis, trans-</i>[Pt(en)(N<sub>3</sub>)<sub>2</sub>, have previously been shown to be stable in the dark but reduced to Pt<sup>II</sup> upon irr

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4

Bolton, R. E. "Azide decomposition in natural product synthesis." Thesis, Imperial College London, 1986. http://hdl.handle.net/10044/1/37947.

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5

Wong, Sang K. "Pharmaceutical studies on aromatic azido compounds." Thesis, Aston University, 1986. http://publications.aston.ac.uk/12461/.

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6

Dang, Thao P. "Biomimetic Modeling of the Nitrogen-centered Radical Postulated to occur during the Inhibition of Ribonucleotide Reductases by 2'-Azido-2'-deoxynucleotides." FIU Digital Commons, 2010. http://digitalcommons.fiu.edu/etd/318.

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Ribonucleotide reductases (RNR) are essential enzymes that catalyze the reduction of ribonucleotides to 2'-deoxyribonucleotides, which is a critical step that produces precursors for DNA replication and repair. The inactivation of RNR, logically, would discontinue producing the precursors of the DNA of viral or cancer cells, which then would consequently end the cycle of DNA replication. Among different compounds that were found to be inhibitors of RNR, 2'-azido-2'-deoxynucleotide diphosphates (N3NDPs) have been investigated in depth as potent inhibitors of RNR. Decades of investigation has su

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7

Schöffler, Claudia. "Propargylazide als Ausgangsmaterialien für Umlagerungsreaktionen und Heterocyclensynthesen." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=964562138.

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8

Firdous, Samia. "Synthesis and Reactions of α-Azido Alcohols". Doctoral thesis, Universitätsbibliothek Chemnitz, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-86012.

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Die vorliegende Arbeit beschäftigt sich mit der Untersuchung von a-Azidoalkoholen, welche über die Reaktion von aliphatischen sowie aromatischen Aldehyden mit HN3 leicht zugänglich sind und die im Gleichgewicht mit den jeweiligen Ausgangsstoffen vorliegen. Bei Raumtemperatur stellt sich dieses Gleichgewicht sehr schnell ein und man erhält spezifische Konzentrationen an Eduktaldehyd, Stickstoffwasserstoffsäure und a-Azidoalkohol. Die Reaktion von Aldehyden mit HN3 generiert dabei ein neues Chriralitätszentrum, wodurch die Umsetzung chiraler Aldehyde, wie z. B. von Zuckerderivaten, zwei anomere

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9

Canbolat, Eylem. "Organocatalytic Resolution Of Racemic Alpha Azido Ketones." Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614602/index.pdf.

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Chiral cyclic alpha azido ketones are very important compounds in organic chemistry. Because, the reduced forms of them are amino alcohols and these amino alcohols are interesting compounds for their biological activities. They have some pharmaceutical activities such as: potassium channel open up properties, treatment of central nervous system, antihypertensive properties, the agent of dopamin receptor activator, hypolipemic agent and dopamine agonist. These types of compounds have highly acidic alpha-protons, and many kinds of reactions can be performed with them. In this study, mainly, sel

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10

Wutke, Jens. "Synthesen und Reaktionen von Ethinylaziden." Doctoral thesis, Universitätsbibliothek Chemnitz, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-61560.

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Gegenstand der vorliegenden Arbeit sind Versuche zur Synthese von 1-Azido-1 alkinen (Ethinylaziden). Diese instabilen Verbindungen zersetzen sich leicht unter Stickstoffabspaltung zu hochreaktiven Carbenen, welche mit verschiedenen Reagenzien, explizit Tolan, Cyclooctin, DMSO sowie DMF, abgefangen werden konnten. Obwohl eine direkte spektroskopische Beobachtung der Titelverbindungen mittels Tieftemperatur-NMR-Spektroskopie nicht verwirklicht werden konnte, gelang der eindeutige Nachweis von Ethinylaziden via deren 1,3-dipolarer Cycloaddition mit dem hochgespannten cyclischen Alkin Cyclooctin.

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Books on the topic "Azidy"

1

United States International Trade Commission. Sodium azide from Japan. U.S. International Trade Commission, 1996.

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2

Wong, Sang Kwang. Pharmaceutical studies on aromatic azido compounds. Aston University. Department of Pharmaceutical Sciences, 1986.

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3

National Institute for Occupational Safety and Health. American Azide Corporation Cedar City, Utah. U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1995.

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4

American Azide Corporation Cedar City, Utah. U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1995.

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5

National Institute for Occupational Safety and Health. American Azide Corporation Cedar City, Utah. U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1995.

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6

Connors, Richard. Synthesis and reactivity of [alpha]-azido carbonyl derivatives. Laurentian University, 1988.

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7

Banert, Klaus. Umlagerungen organischer Azide: Reaktionsmechanismen und Anwendungen in der Synthese. Schäuble, 1993.

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8

Azizy, Ahmad Qodri A. Mereformasi birokrasi: Mengenang pemikiran Prof. A. Qodri Abdillah Azizy, M.A., Ph. D. Penerbit Buku Ilmiah Populer, 2010.

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9

Döwletmämmet Azady adyndaky Türkmen milli dünýä dilleri instituty. Döwletmämmet Azady adyndaky Türkmen Milli Dünýä Dilleri Instituty =: Turkmenskiĭ Nat︠s︡ionalʹnyĭ Institut Mirovykh I︠A︡zykov imeni Dovletmammeta Azadi = Dovletmammet Azadi Turkmen National Institute of World Languages. [Döwletmämmet Azady adyndaky Türkmen Milli Dünýä Dilleri Instituty], 1996.

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10

Bangkit, Perhimpunan Indonesia. Proceeding bedah buku-buku karya Prof. Dr. H. A. Qodry A. Azizy, M.A., "Sang Pemikir Pelaksana", Jakarta, 27 Agustus 2003. Perhimpunan Indonesia Bangkit, 2003.

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Book chapters on the topic "Azidy"

1

Bährle-Rapp, Marina. "azid..., Azid..." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_931.

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2

Miller, M. W., L. F. Audrieth, and W. F. Filbert. "Potassium Azide (Sodium Azide)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132333.ch40.

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3

Liu, Jiping. "Azido Nitrates." In Nitrate Esters Chemistry and Technology. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6647-5_9.

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4

Obenland, C. O., D. J. Mangold, M. P. Marino, T. R. Musgrave, and R. N. Keller. "Ammonium Azide." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132395.ch15.

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Frierson, W. J., and W. F. Filbert. "Ammonium Azide." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132333.ch39.

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6

Gooch, Jan W. "Sodium Azide." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_10819.

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7

Kurt, Thomas L., and Wendy Klein-Schwartz. "Azide poisonings." In Toxicology of Cyanides and Cyanogens. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118628966.ch28.

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8

Gooch, Jan W. "Lead Azide." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6831.

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9

Liu, Jiping. "Azido Liquid Explosives." In Liquid Explosives. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45847-1_6.

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10

Schoffelen, Sanne, and Morten Meldal. "Alkyne-Azide Reactions." In Modern Alkyne Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527677894.ch5.

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Conference papers on the topic "Azidy"

1

"Theoretical Study of the Substituent and Solvent Effects on Azide-Tetrazole Equilibrium of 2-Azido-1,3-benzothiazoles." In International Conference on Chemical, Agricultural and Medical Sciences. International Institute of Chemical, Biological & Environmental Engineering, 2013. http://dx.doi.org/10.15242/iicbe.c1213031.

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2

Zehender, H., E. C. Witte, K. Stegemeier, and A. Patscheke. "IRREVERSIBLE BLOCKADE OF THE THROMBOXANE A2/PROSTAGLANDIN H2 RECEPTOR OF HUMAN PLATELETS BY AZIDO-BSP." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643755.

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Azido-BSP (4-[2-(4-azido-benzenesulphonylamino)-ethyl]phen-oxyacetic acid) is a photolabile derivative of the competitive thromboxane A2 /prostaglandin H2 (TXA2/PGH2) receptor antagonist sulotroban (=BM 13.177). If protected from short wave light, azido-BSP reversibly inhibited the platelet shape change induced by the PGH2 analogue U 46619 but notthe shape change induced by ADP or PAF. Schild analysis revealed an apparent KD=0.2 μM with washed platelets. The irreversible inhibition requiredirradiation of the platelet suspensionwith UVlight (254 nm) for 5 minutes in the presenceof azido-BSP. Af

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3

Puduppakkam, K., and M. Beckstead. "Glycidyl azide polymer combustion modeling." In 37th Joint Propulsion Conference and Exhibit. American Institute of Aeronautics and Astronautics, 2001. http://dx.doi.org/10.2514/6.2001-3429.

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Ucan, Halil Ismet, and Aslihan Yilmaz Obali. "Design of azide-substitued polypyridine ligand." In 2017 IEEE 7th International Conference "Nanomaterials: Application & Properties" (NAP). IEEE, 2017. http://dx.doi.org/10.1109/nap.2017.8190216.

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Farhat, Kamal, Charles Kappenstein, and Yann Batonneau. "Azide-Based Fuel Additives for Ionic Monopropellants." In 45th AIAA/ASME/SAE/ASEE Joint Propulsion Conference & Exhibit. American Institute of Aeronautics and Astronautics, 2009. http://dx.doi.org/10.2514/6.2009-4876.

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Bulian, Chris, and Hobin Lee. "Determination of Lead Azide Arrhenius Kinetics Constants." In 49th AIAA Aerospace Sciences Meeting including the New Horizons Forum and Aerospace Exposition. American Institute of Aeronautics and Astronautics, 2011. http://dx.doi.org/10.2514/6.2011-270.

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Kuluev, A. R., E. A. Zaikina, B. R. Kuluev, and A. V. Chemeris. "Chemically induced mutagenesis of diploid wheat Triticum sinskajae A. Filat. et Kurk." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.140.

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Mutagenesis of Triticum sinskajae was performed using sodium azide. The optimal concentration was 0.1 mM. Changes were observed in the length of the spike and stem in the experimental plants as compared with the control ones.

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8

Dutra, Luiz Gustavo, and Marcus Mandolesi Sá. "Milder Preparation of a g-Azido-a-diazo-b-keto Ester by Consecutive Introduction of Azido and Diazo Groups." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0182-2.

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9

Nonogaki, Saburo, Michiaki Hashimoto, Takao Iwayanagi, and Hiroshi Shiraishi. "Azide-Phenolic Resin Resists Sensitive To Visible Light." In 1985 Microlithography Conferences, edited by Larry F. Thompson. SPIE, 1985. http://dx.doi.org/10.1117/12.947834.

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Hori, Keiichi. "Application of Glycidyl Azide Polymer to Hybrid Rocket Motor." In 45th AIAA/ASME/SAE/ASEE Joint Propulsion Conference & Exhibit. American Institute of Aeronautics and Astronautics, 2009. http://dx.doi.org/10.2514/6.2009-5348.

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Reports on the topic "Azidy"

1

Bracuti, A. J., and C. Y. Manning. The Synthesis of Triaminoguanidinium Azide (TAZ). Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada199160.

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2

Mourad, Jack. The systhesis and photolysis of 1-phenylcyclohexaneacetic acid azide. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2775.

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3

Chen, Chiung-Chu, and Michael McQuaid. A Thermochemical Kinetic-Based Study of Ignition Delays for 2-Azidoethanamine-Red Fuming Nitric Acid Systems: 2-Azido-N-Methylethanamine (MMAZ) Vs. 2-Azido-N,N-Dimethylethanamine (DMAZ). Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada599206.

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McQuaid, Michael J. Computationally Based Measures of Amine Azide Basicity and Their Correlation With Hypergolic Ignition Delays. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada420016.

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McQuaid, Michael J. Computational Characterization of 2-Azidocycloalkanamines: Notional Variations on the Hypergol 2-Azido-N,N-Dimethylethanamine (DMAZ). Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada405699.

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6

McQuaid, Michael J., and Betsy M. Rice. Computational Chemistry-Based Enthalpy-of-Formation, Enthalpy-of-Vaporization, and Enthalpy-of-Sublimation Predictions for Azide-Functionalized Compounds. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada447987.

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7

Cai, Sui X., M. N. Wybourne, and John F. Keana. A Novel Photosensitive Polyimide Resist Consisting of a Soluble Polyimide and a Bis(perfluorophenyl Azide) as a Cross-Linker. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada265998.

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8

Billingsley, James P., and James M. Oliver. The Relevance of the De Broglie Velocity (V sub 1 = h/2md sub 1) to Shock Loading Induced Reactions in Lead Azide. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada246478.

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Health hazard evaluation report: HETA-95-0023-2531, American Azide Corporation, Cedar City, Utah. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1995. http://dx.doi.org/10.26616/nioshheta9500232531.

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