Relevant bibliographies by topics / Azidi

Contents

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

Academic literature on the topic 'Azidi'

Author: Grafiati
Published: 9 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "Azidi"

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Alaa Abdulzahra, Mohammed, Ruaa Wassim Adam, and Hanaa Kadtem Egzar. "New polytetrazole synthesis and adsorption surface investigation based on sulfadiazine grafted polyimine." Himia, Fizika ta Tehnologia Poverhni 15, no. 3 (2024): 420–28. http://dx.doi.org/10.15407/hftp15.03.420.

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The present work concentrates on synthesizing and adsorption surface investigation of polytetrazole polymer (P-T) created from polyimine (P-S) grafted with sulfadiazine drug. The prepared polymer is synthesized by mechanochemical polycondensation reaction between dialdehyde aromatic compound and diamine aromatic compound by applying appropriate polar solvent and glacial acetic acid at (78 °C) as dependent on the polymerization reaction. The synthetic route to prepare tetrazole polymer (P-T) consists off multi chemical reaction process, firstly the synthesis of polyimine backbone (P-S) (4-(((4'
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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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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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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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Sari, Novita Indah Kartika, and Wahyu Indra Duwi Fanata. "RESPON KERAGAAN DAN PRODUKTIVITAS TANAMAN CABAI BESAR (Capsicum annuum L.) TERHADAP KONSENTRASI LARUTAN SODIUM AZIDA." Berkala Ilmiah Pertanian 5, no. 2 (2022): 88. http://dx.doi.org/10.19184/bip.v5i2.29199.

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ABSTRAK
 Cabai besar merupakan salah satu tanaman hortikultura yang memiliki nilai ekonomi yang cukup tinggi di Indonesia. Harga cabai besar, sering kali mengalami kenaikan terutama pada saat hari hari besar. Salah satu yang dapat dilakukan untuk meningkatkan produktivitas cabai besar yaitu dengan menghasilkan kultivar baru yang unggul. Hal yang dapat dilakukan untuk menghasilkan kultivar baru yaitu dapat menggunakan perlakuan mutasi. Perlakuan mutasi yang digunakan dalam penelitian ini yaitu mutasi kimia dengan menggunakan larutan Sodium Azida (NaN3). Perlakuan mutasi Sodium Azida (NaN3)
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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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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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Kapuściński, Szymon, Bindushree Anand, Paulina Bartos, Jose M. Garcia Fernandez, and Piotr Kaszyński. "Tethered Blatter Radical for Molecular Grafting: Synthesis of 6-Hydroxyhexyloxy, Hydroxymethyl, and Bis(hydroxymethyl) Derivatives and Their Functionalization." Molecules 27, no. 4 (2022): 1176. http://dx.doi.org/10.3390/molecules27041176.

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Synthetic access to 7-CF3-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl radicals containing 4-(6-hydroxyhexyloxy)phenyl, 4-hydroxymethylphenyl or 3,5-bis(hydroxymethyl)phenyl groups at the C(3) position and their conversion to tosylates and phosphates are described. The tosylates were used to obtain disulfides and an azide with good yields. The Blatter radical containing the azido group underwent a copper(I)-catalyzed azide–alkyne cycloaddition with phenylacetylene under mild conditions, giving the [1,2,3]triazole product in 84% yield. This indicates the suitability of the azido derivative for grafti
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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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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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Dissertations / Theses on the topic "Azidi"

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LO, CONTE Mauro. "SINTESI DI BIOISOSTERI DEGLI OLIGOMANNOSI CON POTENZIALE ATTIVITA’ ANTITUBERCOLARE." Doctoral thesis, Università degli studi di Ferrara, 2010. http://hdl.handle.net/11392/2389182.

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Mycobacterium tuberculosis is the cause of the deadly infectious disease, tuberculosis (TB). According to the World Health Organization, nearly one–third of the world's population has been exposed to the tuberculosis pathogen and nearly 1.6 million deaths result every year. TB is, in addition, the leading infectious killer of people living with HIV/AIDS. Recent outbreaks of drug-resistant TB in many industrialized nations have led to a new interest in the disease, and basic research and drug development have again become priorities. The Mycobacterium organism possesses a complex cell wal
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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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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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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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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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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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Wong, Sang K. "Pharmaceutical studies on aromatic azido compounds." Thesis, Aston University, 1986. http://publications.aston.ac.uk/12461/.

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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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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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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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Books on the topic "Azidi"

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Stefan, Bräse, and Banert Klaus, eds. Organic azides: Syntheses and applications. Wiley, 2009.

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Nahal, Chaman. Azadi. Penguin Books, 2001.

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Singh, Khushwant. Azadi. Nigarshaat, 2004.

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Bhatt, Dolat. Azadi andolan. Kothari, 1988.

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Kamleshur. Azadi mubarak. Satiya academy, 2001.

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Jouan, Yves. Azadi: Poèmes. Dumerchez, 1995.

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Sevim, Ali. Azimi Tarihi. Turk Tarih Kurumu Basimevi, 1988.

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Kychanov, E. I. Vlastiteli Azii. Vostochnai︠a︡ literatura RAN, 2004.

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Zolott͡sev, Stanislav Aleksandrovich. Zov Azii. Izd-vo "Adib", 1987.

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Rerikh, Nikolaĭ Konstantinovich. Legendy Azii. "ĖKSMO", 2014.

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Book chapters on the topic "Azidi"

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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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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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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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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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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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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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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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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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Bodanszky, Miklos, and Agnes Bodanszky. "The Azide Process." In The Practice of Peptide Synthesis. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85055-4_6.

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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 "Azidi"

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Kwon, Jieun, Syed Zahid Hassan, and Dae Sung Chung. "Intrinsically stretchable High-k dielectrics metal oxide transistor with azide-functionalized coordination ligand for skin electronics." In Image Sensing Technologies: Materials, Devices, Systems, and Applications XII, edited by Nibir K. Dhar, Achyut K. Dutta, and Sachidananda R. Babu. SPIE, 2025. https://doi.org/10.1117/12.3059188.

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Birca, Natalia, and Veaceslav Kulcitki. "Late stage functionalization of cyclic terpenoids by atom transfer radical addition. A convenient route towards nitrogen heterocycles." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab12.

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Terpens are a class of widely spread natural compounds with a broad range of biological properties, showing ‘drug-like’ chemical properties, including lipophilicity, interesting molecular geometry, alkylating center reactivity etc [1]. Nevertheless, nitrogen-containing terpens, which can show diverse functionality and biological activity in living cells, are rare in natural sources. We present in this communication the atom transfer radical additions performed on relevant terpene derivatives of labdane and drimane framework, compounds 1-3, and resulting in a series of azido-compounds. Carboazi
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"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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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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Pajic, Tanja, Miroslav Zivic, Mihailo Rabasovic, Aleksandar Krmpot, and Natasa Todorovic. "THE DAMPENING OF LIPID DROPLET OSCILLATORY MOVEMENT IN NITROGEN STARVED FILAMENTOUS FUNGI BY A LOW DOSE OF MITOCHONDRIAL RESPIRATION INHIBITOR." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac,, 2021. http://dx.doi.org/10.46793/iccbi21.226p.

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Lipid droplets (LDs) are small mobile organelles conserved in all eukaryotic cells. We wanted to test if the LD movement can be muffled by an incomplete inhibition of mitochondrial respiration, induced by treating hyphae of filamentous fungus Phycomyces blakesleeanus with 0.5 mM sodium azide. Nitrogen starved hyphae were used, in order to obtain LDs in larger sizes and numbers. The data obtained unequivocally showed: 1. Sodium azide treatment dramatically reduces the LD velocity and the distances LDs travel; 2. LDs in both controls and in azide-treated hyphae oscillate in a small confined spac
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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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Campillo Robles, Jose Miguel, and Laura Oca. "Geruzatzerik gabeko berun-azido bateriak." In I. Ikergazte. Nazioarteko ikerketa euskaraz. UEU arg, 2015. http://dx.doi.org/10.26876/ikergazte.i.74.

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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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De la Caba Ciriza, Koro, Pedro Guerrero Manso, Alaitz Etxabide Etxeberria, Itsaso Leceta Lasa, and Jone Uranga Gama. "Azido zitrikoz eraldatutako arrain-gelatinazko filmak." In II. Ikergazte. Nazioarteko ikerketa euskaraz. UEU arg, 2017. http://dx.doi.org/10.26876/ikergazte.ii.03.08.

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Coombe, Robert D. "Azide reactions for advanced chemical lasers." In OSA Annual Meeting. Optica Publishing Group, 1986. http://dx.doi.org/10.1364/oam.1986.wh1.

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An efficient short-wavelength chemical laser will be a device which couples a highly constrained chemical pumping mechanism with an atomic or molecular species whose spectroscopic characteristics are appropriate for lasing. Research in the past several years has identified a number of candidates (e.g., interhalogens, group VI atoms and molecules, CN, NO, and others) which are capable of lasing in the UV or visible regions. Recent work in our laboratory has sought means by which the very highly constrained reactions of azide radicals may be used to pump these known candidate systems. The electr
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Reports on the topic "Azidi"

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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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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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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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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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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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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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