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Journal articles on the topic 'Hydrazoic'

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1

Asghari, Sakineh, Ali Asghar Gouran, Davood Farmanzadeh, and Tahereh Abdollahi. "Investigating the reaction pathways of chemical functionalization of C20 fullerene by nitrile oxide and azide; A computational study." Journal of Theoretical and Computational Chemistry 17, no. 01 (2018): 1850003. http://dx.doi.org/10.1142/s0219633618500037.

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In this study, the interactions between nitrile oxide (fulminic acid) and azide (hydrazoic acid) with the C[Formula: see text] fullerene were investigated and their priority in reacting and functionalizing surface of this fullerene were compared with each other. The results show that the 1,3-dipolar cycloaddition reaction between fulminic acid and C[Formula: see text] fullerene could occur faster than this reaction by hydrazoic acid. Therefore, nitrile oxide group as a dipole is much preferred compared to the azide functional group in reacting with the surface of C[Formula: see text] fullerene
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2

Vávra, K., P. Kania, J. Koucký, Z. Kisiel, and Š. Urban. "Rotational spectra of hydrazoic acid." Journal of Molecular Spectroscopy 337 (July 2017): 27–31. http://dx.doi.org/10.1016/j.jms.2017.04.002.

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3

Donati, C., RH Prager, and B. Weber. "Potential GABAB Receptor Antagonists. III. Folded Baclofen Analogs Based on Phthalide." Australian Journal of Chemistry 42, no. 6 (1989): 787. http://dx.doi.org/10.1071/ch9890787.

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Possible analogues of baclofen, 3-aminomethyl-5-chloro-, 3-aminomethyl-6-chloro- and 3-aminomethyl-5,6-dichloro-isobenzofuran-1(3H)-one, have been prepared for evaluation as antispasticity agents. The corresponding 3-hydroxyisobenzofuran-l(3H)-one was reacted with ethyl acetoacetate under acidic conditions, and the keto ester hydrolysed and decarboxylated to give the 3-(2-oxopropyl)isobenzofuran-l(3H)-one; this was treated with hydrazoic acid, and the product was hydrolysed. A parallel series of (3-oxo-1,3-dihydroisobenzofuran-1-y1)glycines was obtained by treating the keto ester first with hy
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4

Betterton, Eric A., and Jill L. Robinson. "Henry’s Law Coefficient of Hydrazoic Acid." Journal of the Air & Waste Management Association 47, no. 11 (1997): 1216–19. http://dx.doi.org/10.1080/10473289.1997.10464060.

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5

Couladouros, Elias A., and Costas D. Apostolopoulos. "1,4-Reductive Addition of Hydrazoic Acid." Synlett 1996, no. 04 (1996): 341–42. http://dx.doi.org/10.1055/s-1996-5411.

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6

Ongstad, A. P., R. D. Coombe, D. K. Neumann, and D. J. Stech. "Photochemistry of ozone/hydrazoic acid mixtures." Journal of Physical Chemistry 93, no. 2 (1989): 549–52. http://dx.doi.org/10.1021/j100339a013.

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7

Gafarov, A. N. "Hydrazoic acid in the Mannich reaction." Russian Chemical Bulletin 58, no. 10 (2009): 2169–72. http://dx.doi.org/10.1007/s11172-009-0296-8.

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8

Kabalka, George W., David A. Henderson, and Rajender S. Varma. "Reaction of organoboranes with hydrazoic acid." Organometallics 6, no. 6 (1987): 1369–70. http://dx.doi.org/10.1021/om00149a046.

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9

L'abbé, Gerrit, Jean-Paul Dekerk, and Peter van Stappen. "Addition of Hydrazoic Acid to Dimethyl Acetylenedicarboxylate." Bulletin des Sociétés Chimiques Belges 90, no. 10 (2010): 1073–74. http://dx.doi.org/10.1002/bscb.19810901012.

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10

Hussain, S., M. Noor Saleh, J. Forsberg, and L. Ehrenberg. "Mutagenicity of hydrazoic acid emanated from azide solution." Hereditas 87, no. 1 (2009): 127–28. http://dx.doi.org/10.1111/j.1601-5223.1977.tb01254.x.

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11

Chong, D. P. "Theoretical study of hydrazoic acid and methyl azide." Chemical Physics Letters 175, no. 5 (1990): 525–30. http://dx.doi.org/10.1016/0009-2614(90)85575-w.

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12

COULADOUROS, E. A., and C. D. APOSTOLOPOULOS. "ChemInform Abstract: 1,4-Reductive Addition of Hydrazoic Acid." ChemInform 27, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199633149.

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13

Hoff, S., and A. P. Blok. "Cycloaddition of isothiocyanates with diazomethane and hydrazoic acid." Recueil des Travaux Chimiques des Pays-Bas 93, no. 12 (2010): 317–19. http://dx.doi.org/10.1002/recl.19740931205.

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14

Ibtehal K. Abdullah and Meaad K. Buniya. "Preparation and Identification of some heterocyclic compounds from cyano compounds." Tikrit Journal of Pure Science 20, no. 5 (2023): 96–105. http://dx.doi.org/10.25130/tjps.v20i5.1245.

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This article included prepared cyano acetic acid hydrazid from interaction cyano ethylacetate with hydrate hydrazen, and interaction with 2- acytel thiophene and 2- acytelpyridine it will formation of hydrazide- hydrazone derivative (I, II), and through the undergo the compounds (I,II) for chain of interactions with different chemical materials then enclosed cyclo formed derivative of (arylidene ,coumarin , aryl hydrazon , thiophene ) .
 Prepared compounds have been studied and Identification by physical and spectral means.
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15

Tokoro, Roberto, Mauro Bertotti, and Lúcio Angnes. "Polarographic studies of indium(III) in aqueous medium of sodium azide." Canadian Journal of Chemistry 73, no. 2 (1995): 232–40. http://dx.doi.org/10.1139/v95-032.

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In this paper, some aspects of the polarography of indium(III) in azide/hydrazoic acid buffer are presented. The electrode process is mostly governed by diffusion in the complexing medium. Nevertheless, for controlled-potential coulometry (involving a large time window) a catalytic process was observed, ascribed to the reaction of the hydrazoic acid and indium amalgam. The stability of azide complexes of In(III) was studied polarographically, and the formation of four mononuclear species was confirmed by computational analysis of data obtained from polarograms of In(III) in different azide con
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16

Porezag, Dirk, Mark R. Pederson, and Amy Y. Liu. "Adsorption and dissociation of hydrazoic acid on Al(111)." Physical Review B 61, no. 19 (2000): 13230–34. http://dx.doi.org/10.1103/physrevb.61.13230.

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17

Bendtsen, Jørgen, та Flemming M. Nicolaisen. "Infrared spectrum of the ν4 band of hydrazoic acid". Journal of Molecular Spectroscopy 133, № 1 (1989): 193–200. http://dx.doi.org/10.1016/0022-2852(89)90253-1.

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18

Ponnuswamy, S., A. Akila, and D. Kiruthiga Devi. "Facile Denitrosation of Cyclic N-Nitrosamines with Hydrazoic Acid." Synthetic Communications 45, no. 17 (2015): 2030–34. http://dx.doi.org/10.1080/00397911.2015.1063654.

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19

G., M. ABOU-ELENIEN, A. ABD EL-RAHMAN H., and S. EL-BASIOUNY M. "Polarisation Behaviour of Mild Steel in Sulphuric Acid Solutions containing Sodium Azide." Journal of Indian Chemical Society Vol. 67, Sep 1990 (1990): 726–29. https://doi.org/10.5281/zenodo.6243658.

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Chemistry Department, Faculty of Science, Cairo University, Giza, A. R. Egypt <em>Manuscript received 22 December 1989, revised 20 April 1990, accepted 3 July 1990</em> The polarisation behaviour of iron in deoxygenated sulphuric acid solutions in absence and presence of NaN<sub>3</sub> was studied. The presence of NaN<sub>3</sub> was found to shift the cathodic branches of the polarisation curves much more than the anodic ones to higher current densities. The cathodic and anodic Tafel slopes in absence and presence of NaN<sub>3</sub> were found to be the same. The corrosion rate and corrosion
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20

Lin, Sheng H., and Cheng P. Huang. "Adsorption of hydrazoic acid from aqueous solution by macroreticular resin." Journal of Hazardous Materials 84, no. 2-3 (2001): 217–28. http://dx.doi.org/10.1016/s0304-3894(01)00228-x.

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21

Forohar, Farhad, Victor J. Bellitto, William M. Koppes, and Craig Whitaker. "The adsorption of hydrazoic acid on single-walled carbon nanotubes." Materials Chemistry and Physics 112, no. 2 (2008): 427–31. http://dx.doi.org/10.1016/j.matchemphys.2008.05.076.

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22

Schönnenbeck, G., H. Biehl, F. Stuhl, U. Meier, and V. Staemmler. "Vuv photolysis of hydrazoic acid: Absorption and fluorescence excitation spectra." Journal of Chemical Physics 109, no. 6 (1998): 2210–19. http://dx.doi.org/10.1063/1.476789.

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23

Cacace, Fulvio, Marina Attina, Maurizio Speranza, Giulia de Petris, and Felice Grandinetti. "Concerning the proton affinity of hydrazoic acid and methyl nitrate." Journal of Organic Chemistry 58, no. 14 (1993): 3639–42. http://dx.doi.org/10.1021/jo00066a013.

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24

Titova, I. E., V. S. Poplavskii, G. I. Koldobskii, V. A. Ostrovskii, V. D. Nikolaev, and G. B. Erusalimskii. "Tetrazoles. 21. Reaction of benzonitrile with salts of hydrazoic acid." Chemistry of Heterocyclic Compounds 22, no. 8 (1986): 880–83. http://dx.doi.org/10.1007/bf01175064.

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25

Russell,, John N., Victor M. Bermudez, and Andrés Leming. "Adsorption and Thermal Decomposition of Hydrazoic Acid on Al(111)." Langmuir 12, no. 26 (1996): 6492–500. http://dx.doi.org/10.1021/la960505w.

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26

Breton, Gary W., Kimberlee A. Daus, and Paul J. Kropp. "Surface-mediated reactions. 2. Addition of hydrazoic acid to alkenes." Journal of Organic Chemistry 57, no. 24 (1992): 6646–49. http://dx.doi.org/10.1021/jo00050a053.

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27

Prager, RH, C. Tsopelas, and T. Heisler. "A Simple Synthesis of Amphimedine." Australian Journal of Chemistry 44, no. 2 (1991): 277. http://dx.doi.org/10.1071/ch9910277.

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The marine alkaloid amphimedine has been synthesized by a short sequence of reactions commencing from the known indenopyridinedione (2). Reaction with 4-pyridyllithium, followed by hydrazoic acid treatment, gave 5-(4-pyridyl)-3,6-phenanthrolin-4(3H)-one (12) which was converted into the chlorophenanthroline. The methyl-substituted fluorosulfonate salt of this compound was specifically oxidized by alkaline ferricyanide. Conversion of the pyridone into the nitrile gave the precursor which was cyclized to amphimedine by polyphosphoric acid.
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28

Gerry, M. C. L., N. Heineking, H. Mäder, and H. Dreizler. "Resolution of the 14N Nuclear Quadrupole Hvperfine Structure in the Rotational Spectrum of Hydrazoic Acid, HN3, and Evaluation of the Rotational Constants of H15NNN and HNN15N." Zeitschrift für Naturforschung A 44, no. 11 (1989): 1079–86. http://dx.doi.org/10.1515/zna-1989-1107.

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Microwave Fourier transform spectra have been measured for hydrazoic acid as its normal isotopomer, H14N3, and two substituted isotopomers, H15N14N14N and H14N14N15N. The 14N quadrupole hyperfine structure has been resolved in all cases, and the quadrupole coupling constants of all 14N atoms have been determined. They are compared with those from ab initio predictions. Rotational constants A have been evaluated accurately for the first time for the two 15N species, and have been used to confirm a previously published structure
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29

Klimochkin, Yuri, Ilya Tkachenko, and Victor Rybakov. "Convenient Synthesis of Ethyl 5-Oxohomoadamantane-4-carboxylate: A Useful Precursor of Polyfunctional Homoadamantanes." Synthesis 51, no. 06 (2018): 1482–90. http://dx.doi.org/10.1055/s-0037-1610312.

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A facile and convenient synthesis of ethyl 5-oxohomoadamantane-4-carboxylate is reported, and its chemical properties as a cage analogue of acetoacetic ester are investigated. Various derivatives of homoadamantane were synthesized through the reaction of 5-oxohomoadamantane-4-carboxylate with electrophilic agents, binucleophiles, and hydrazoic acid. Some new unusual products were obtained by the reaction of that β-keto ester with nitric acid and nitrosyl chloride. Cage compounds synthesized could be used as precursors for the diverse condensed heterocyclic compounds with potential viral ion ch
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30

DEB, Jyotirmoy, Debolina PAUL, David PEGU, and Utpal SARKAR. "Adsorption of Hydrazoic Acid on Pristine Graphyne Sheet: A Computational Study." Acta Physico-Chimica Sinica 34, no. 5 (2018): 537–42. http://dx.doi.org/10.3866/pku.whxb201710161.

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31

Furton, Kenneth G., J. Howard Purnell, and Geoffrey Stedman. "Stability constants of hydrazoic acid–tributyl phosphate complexes in hexadecane solution." J. Chem. Soc., Faraday Trans. 86, no. 21 (1990): 3561–65. http://dx.doi.org/10.1039/ft9908603561.

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32

Puskar, Mark A., Scott M. Fergon, and Lawrence H. Hecker. "A SHORT-TERM SOLID SORBENT DETERMINATION OF HYDRAZOIC ACID IN AIR." American Industrial Hygiene Association Journal 52, no. 1 (1991): 14–19. http://dx.doi.org/10.1080/15298669191364253.

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33

Avdeenko, A. P., and Yu V. Menafova. "Reactivity of N-arylsulfonyl-1,4-benzoquinone imines. Reaction with hydrazoic acid." Russian Journal of Organic Chemistry 42, no. 3 (2006): 403–5. http://dx.doi.org/10.1134/s1070428006030110.

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34

Besset, Céline, Stéphane Chambert, Bernard Fenet, and Yves Queneau. "Direct azidation of unprotected carbohydrates under Mitsunobu conditions using hydrazoic acid." Tetrahedron Letters 50, no. 50 (2009): 7043–47. http://dx.doi.org/10.1016/j.tetlet.2009.09.173.

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35

Akhmetov, A. R., A. R. Tuktarov, U. M. Dzhemilev, I. R. Yarullin, and L. A. Gabidullina. "First example of the interaction of fullerene C60 with hydrazoic acid." Russian Chemical Bulletin 60, no. 9 (2011): 1885–87. http://dx.doi.org/10.1007/s11172-011-0284-7.

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36

Jonathan, N. B. H., P. J. Knight, and A. Morris. "UHV studies of the adsorption of hydrazoic acid on Si(100)." Surface Science 275, no. 1-2 (1992): L640—L644. http://dx.doi.org/10.1016/0039-6028(92)90634-i.

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37

Chu, Jason C. S., Y. Bu, and M. C. Lin. "Spectroscopy and reactions of hydrazoic acid on silicon single crystal surfaces." Surface Science 284, no. 3 (1993): 281–90. http://dx.doi.org/10.1016/0039-6028(93)90499-a.

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38

Gericke, Karl Heinz, Tobias Haas, Michael Lock, Robert Theinl, and Franz Josef Comes. "Hydrazoic acid(~A1A'') hypersurface at excitation energies of 4.0-5.0 eV." Journal of Physical Chemistry 95, no. 16 (1991): 6104–11. http://dx.doi.org/10.1021/j100169a013.

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39

Wiss, Jacques, Christian Fleury, Christoph Heuberger, Ulrich Onken, and Martin Glor. "Explosion and Decomposition Characteristics of Hydrazoic Acid in the Gas Phase." Organic Process Research & Development 11, no. 6 (2007): 1096–103. http://dx.doi.org/10.1021/op7000645.

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40

Wang, Jeng-Han, M. C. Lin, and Ying-Chieh Sun. "Reactions of Hydrazoic Acid on TiO2Nanoparticles: an Experimental and Computational Study." Journal of Physical Chemistry B 109, no. 11 (2005): 5133–42. http://dx.doi.org/10.1021/jp0458046.

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41

Soni, Vimal, and Raj N. Mehrotra. "Mechanism of the oxidation of hydrazoic acid by tetrachloroaurate(III) ion." Transition Metal Chemistry 33, no. 3 (2008): 367–76. http://dx.doi.org/10.1007/s11243-007-9052-9.

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42

Ananiev, A. "Kinetics of the platinum catalyzed hydrazoic acid decomposition in acidic media." Applied Catalysis A: General 257, no. 2 (2004): 151–56. http://dx.doi.org/10.1016/j.apcata.2003.07.003.

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43

Xia, Qi Ying, He Ming Xiao, Xue Hai Ju, and Xue Dong Gong. "DFT study on cooperativity in the interactions of hydrazoic acid clusters." International Journal of Quantum Chemistry 94, no. 5 (2003): 279–86. http://dx.doi.org/10.1002/qua.10643.

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44

Ponnuswamy, S., A. Akila, and D. Kiruthiga Devi. "ChemInform Abstract: Facile Denitrozation of Cyclic N-Nitrosamines with Hydrazoic Acid." ChemInform 46, no. 49 (2015): no. http://dx.doi.org/10.1002/chin.201549154.

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45

Afaque, Shala, M. H. Ansari та M. S. Siddiqui. "Reaction of Hydrazoic Acid on γ- and β-Oxoolefinic Fatty Acids". Fett Wissenschaft Technologie/Fat Science Technology 90, № 12 (1988): 470–75. http://dx.doi.org/10.1002/lipi.19880901203.

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46

Avdeenko, A. P., and S. A. Zhukova. "ChemInform Abstract: Reaction of N-Arylsulfonyl-p-quinonimines with Hydrazoic Acid." ChemInform 32, no. 21 (2010): no. http://dx.doi.org/10.1002/chin.200121054.

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47

BRIDGES, A. S., R. GREEF, N. B. H. JONATHAN, A. MORRIS, and G. J. PARKER. "ELLIPSOMETRIC STUDIES OF VERY LOW PRESSURE THERMAL CVD GROWN SILICON NITRIDE THIN FILMS USING HYDRAZOIC ACID AND DICHLOROSILANE." Surface Review and Letters 01, no. 04 (1994): 573–76. http://dx.doi.org/10.1142/s0218625x94000692.

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High quality silicon nitride thin films have been grown using dichlorosilane and hydrazoic acid (ratio 1:5) at a total ambient growth pressure of 1×10–4 Torr. Sequential growth studies of successive CVD nitride films over the 974-1068 K temperature range revealed an activation energy of 84 kJmol –1. Film thicknesses and refractive indices were obtained using in situ real-time ellipsometry, and the majority of the grown films displayed a refractive index of 2.0. Ellipsometric data for the growth of an 8 Å thermal-nitride film with a refractive index of 2.0 are also given.
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48

Chen, Xiao-fang, Kun Yang, and Ke-li Han. "Theoretical Study of 1,3-Dipolar Cycloaddition of Hydrazoic Acid to Substituted Ynamines." Chinese Journal of Chemical Physics 22, no. 2 (2009): 143–48. http://dx.doi.org/10.1088/1674-0068/22/02/143-148.

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49

Donkor, A., RH Prager, and MJ Thompson. "Heterocyclic Synthesis With Azides. I. The Reaction of Hydrazoic Acid With Ethoxymethylenemalonate." Australian Journal of Chemistry 45, no. 10 (1992): 1571. http://dx.doi.org/10.1071/ch9921571.

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Reaction of diethyl ethoxymethylenemalonate with sodium azide in trifluoroacetic acid at 20� gives ethyl 5-ethoxyisoxazole-4-carboxylate (67%), diethyl cyanomalonate (21%) and diethyl ethoxyaminomethylenemalonate (5%). The last compound and its tautomer are converted into ethyl 1-ethoxy-3-oxo-2,3-dihydro-1H-pyrazole-4-carboxylate. The product structures have been confirmed by synthesis or degradation.
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50

Han, Keping, and D. Howard Fairbrother. "Surface nitridation of nickel using hydrazoic acid (HN3) and nitrogen ion implantation." Applied Surface Science 195, no. 1-4 (2002): 229–35. http://dx.doi.org/10.1016/s0169-4332(02)00560-3.

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