Relevant bibliographies by topics / Hydrazoic

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

Academic literature on the topic 'Hydrazoic'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Hydrazoic"

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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Hydrazoic"

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Nakai, Takashi S. M. Massachusetts Institute of Technology. "Asymmetric synthesis of amines by the catalytic enantioselective additions of hydrazoic acid to ketenes." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/41770.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2007.<br>Includes bibliographical references.<br>The development of a planar-chiral catalyst for the enantioselective additions of HN3 to hindered ketenes was investigated. It was demonstrated that a new planar-chiral catalyst (1.5) is an excellent catalyst for the enantioselective addition of HN3 to hindered ketenes, en route to enantioenriched amines. The addition of HN3 to a ketene is likely occurring by the Bronsted acid catalysis mechanism. The evidence in support of the Bronsted acid catalysis mechanism include ste
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Bridges, Andrew Simon. "Very low pressure MOCVD growth of III-N and IV-N epitaxial layers using novel nitrogen precursor, hydrazoic acid." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242566.

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Bertotti, Mauro. "Estudos polarográficos envolvendo aquo-íons de molibdênio em meio sulfúrico e caracterização de processo catalítico na presença de ácido azotídrico." Universidade de São Paulo, 1992. http://www.teses.usp.br/teses/disponiveis/46/46133/tde-17082010-105830/.

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A literatura cita o aparecimento de onda catalítica polarográfica do Mo(VI) na presença de NO-3. Há menção na literatura sobre comportamento semelhante entre o ácido azotídrico e o ácido nítrico em relação ao poder de oxidação. Seguindo uma linha de pesquisa da área de Química Analítica deste Instituto, procedeu-se a estudos envolvendo a existência de onda polarográfica de natureza catalítica do Mo(VI) na presença de HN3. Os trabalhos foram desenvolvidos utilizando-se técnicas como espectrofotometria, polarografia TAST e de pulso (normal e diferencial) e coulometria a potencial controlado, com
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Jadhav, Abhijit V. "Crosslinking of polyaniline with aryl azides and the photolysis of vinyl azides and azidopropanones." University of Cincinnati / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1204666531.

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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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Gellermann, Eike. "Silylhydrazine und -hydrazone Insertionsreaktionen und Isomerisierung /." [S.l. : s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=963676393.

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Juon, Heinz. "Genotoxizität von Hydrazin-Derivaten bei Drosophila melanogaster /." Zürich, 1986. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=8130.

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Buff, Heiko. "Hydrazone als Aza-Enamine in der Nenitzescu-Reaktion." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=963417282.

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Klein, Jörg Martin. "Dynamic combinatorial chemistry of hydrazone and disulfide macrocycles." Thesis, University of Cambridge, 2011. https://www.repository.cam.ac.uk/handle/1810/252248.

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Köhler, Brigitte. "Von der Koordinationschemie der Azaphosphole zur Koordinationschemie funktionalisierter Hydrazone." Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-104523.

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Books on the topic "Hydrazoic"

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Shahrouri, Tawfiq. Hydrazin- und Hydroxylaminderivate als NO-Donatoren. [s.n.], 1996.

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Perner, Monika. Untersuchungen an dipolaren Hydroxylamin- und Hydrazin-Verbindungen. [s.n.], 1985.

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Patai, Saul, ed. The Chemistry of the Hydrazo, Azo and Azoxy Groups. John Wiley & Sons, Ltd, 1997. http://dx.doi.org/10.1002/0470023503.

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Knopp, Monika. Diastereo- und enantioselektive Caroll- und Aza-Claisen-Umlagerung mit Hilfe der SAMP, RAMP-Hydrazon-Methode. [s.n.], 1996.

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Meiers, Michaela Elisabeth. Diastereo- und enantioselektive Synthese von C2symmetrischen 1,n-Diaminen durch nucleophile 1,2-Addition an Dialdehyd-SAMP-Hydrazone. [s.n.], 1997.

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Aachen, Rheinisch-Westfälische Technische Hochschule, ed. Enantioselektive Synthese von [alpha]-, [beta]- und [omega]-Aminoacetalen [Omega-Aminoacetalen] und -Aminosäuren durch 1,2-Addition an Aldehyd-SAMP/RAMP-Hydrazone. [s.n.], 1994.

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Rendenbach, Beatrice. Asymmetrische Michael-Additionen via SAMP-/RAMP-Hydrazone - diastereo- und enantioselektive Synthese von substituierten 5-Oxoestern [Oxoestern] und d-Lactonen [Delta-Lactonen]. [s.n.], 1987.

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8

Karafiat, Ute. Synthese und Reaktionen von Hydrazid-hydrazonen. 1989.

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Patai, Saul E. Chemistry of Hydrazo Azo and Azoxy Groups. Wiley & Sons, Limited, John, 2010.

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Patai, S., and Saul Patai. Chemistry of the Hydrazo, Azo and Azoxy Groups. Wiley & Sons, Incorporated, John, 2000.

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Book chapters on the topic "Hydrazoic"

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Lazny, Ryszard. "Hydrazone Linker Units." In Linker Strategies in Solid-Phase Organic Synthesis. John Wiley & Sons, Ltd, 2009. http://dx.doi.org/10.1002/9780470749043.ch10.

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Li, Jie Jack. "Japp-Klingemann hydrazone synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_154.

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Li, Jie Jack. "Japp–Klingemann hydrazone synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_142.

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Li, Jie Jack. "Japp-Klingemann hydrazone synthesis." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_144.

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Li, Jie Jack. "Japp–Klingemann hydrazone synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_133.

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Buss, Joan L., Marcelo Hermes-Lima, and Prem Ponka. "Pyridoxal Isonicotinoyl hydrazone and its analogues." In Iron Chelation Therapy. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0593-8_11.

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Tang, Jinkui, and Peng Zhang. "Hydrazone-Based Lanthanide Single-Molecule Magnets." In Lanthanide Single Molecule Magnets. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-46999-6_5.

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Horowitz, A., and L. A. Rajbenbach. "Radiation chemistry of hydrazo and azo compounds." In Chemistry of Functional Groups. John Wiley & Sons, Ltd., 2013. http://dx.doi.org/10.1002/9780470686317.ch10.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with polydentate hydrazonic ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_353.

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Melnyk, Oleg, Nathalie Ollivier, Christophe Olivier, Catherine Gouyette, Tam Huynh-Dinh, and Hélène Gras-Masse. "Synthesis of Oligodeoxynucleotide-Peptide Conjugates Using Hydrazone Chemical Ligation." In Peptides: The Wave of the Future. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_48.

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Conference papers on the topic "Hydrazoic"

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Milenković, Dejan, Marko Antonijević, Edina Avdović, Dušica Simijonović, and Zoran Marković. "Design, in Silico Evaluation, and Toxicological Assessment of $N$-Protocatechoyl Hydrazone Derivatives as Potential EGFR Kinase Inhibitors." In 2024 IEEE 24th International Conference on Bioinformatics and Bioengineering (BIBE). IEEE, 2024. https://doi.org/10.1109/bibe63649.2024.10820446.

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Amberger, Brent, Robert McMahon, R. Woods, and Brian Esselman. "MILLIMETER-WAVE SPECTROSCOPY OF HYDRAZOIC ACID (HN3)." In 69th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.wj05.

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Amberger, Brent, Robert McMahon, Brian Esselman, and R. Woods. "MILLIMETER-WAVE SPECTROSCOPY AND GLOBAL ANALYSIS OF THE LOWEST EIGHT VIBRATIONAL STATES OF DEUTERATED HYDRAZOIC ACID (DN3)." In 70th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.fe02.

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Woods, R., Robert McMahon, Brian Esselman, and Brent Amberger. "TOWARDS A GLOBAL FIT OF THE COMBINED MILLIMETER-WAVE AND HIGH RESOLUTION FTIR DATA FOR THE LOWEST EIGHT VIBRATIONAL STATES OF HYDRAZOIC ACID (HN3)." In 70th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.fe01.

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Owen, Andrew, Robert McMahon, R. Woods, John Stanton, Brian Esselman, and Nitai Sahoo. "IMPROVED SEMI-EXPERIMENTAL EQUILIBRIUM STRUCTURE DETERMINATION AND THEORETICAL PREDICTION OF HYDRAZOIC ACID (<span class="roman">HN</span><sub><span class="roman">3</span></sub>)." In 2021 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.te04.

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Branković, Jovica, Vesna Milovanović, and Vladimir P. Petrović. "CYCLOOXYGENASE-2 AS „IN SILICO“ TARGET OF PHENOLIC HYDRAZONE- TYPE DERIVATIVES." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.324b.

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In the present work, a series of phenolic hydrazone analogs were investigated in silico for their potential inhibitory activity toward COX-2. These examinations were based on the capability of hydrazone-based compounds to interact with numerous enzymes, as well as on their versatile biological features and therapeutical applications. COX-2 was selected due to its involvement in the inflammation and carcinogenesis processes. Regarding this, COX-2 represents a valid target for the development of compounds that could block the formation of harmful inflammation mediators.
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Liphardt, Martin, Brian Jones, Stephen Ducharme, J. M. Takacs, Lei Zhang, and R. V. Athalye. "Photorefractive characterization of polymers." In OSA Annual Meeting. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/oam.1993.mxx.6.

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Branković, Jovica, Zorica D. Petrović, and Vladimir P. Petrović. "In silico antibiofilm potency of phenolic N-acyl hydrazones against selected bacterial strains." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.495b.

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In the present work, fourteen phenolic hydrazone derivatives were evaluated for their in silico inhibitory activity against selected P. aeruginosa and S. maltophilia proteins involved in drug resistance and biofilm formation. Molecular docking analysis revealed the highest binding affinity of analogs n (-8.4 kcal/mol) and h (-7.3 kcal/mol) towards P. aeruginosa 7m1m and 7m1l proteins, respectively. In the case of S. maltophilia, analog k (-8.4 kcal/mol) expressed the highest binding affinity to 6qw7, whereas for 6uaf, the lowest binding energy was calculated for derivative d (-8.1 kcal/mol). T
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Marques, Monique Ferreira, and Silvio Cunha. "Synthesis of Cyclic Azo- and Hydrazo-Enaminones." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0305-1.

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Ducharme, Stephen, Brian Jones, Martin Liphardt, et al. "Photorefractive Properties of Bisphenol-A-4,4'-Nitroaminostilbene Mixed with Diethylaminobenzaldehyde-Diphenyl Hydrazone." In Photorefractive Materials, Effects, and Devices II. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/pmed.1993.tha.1.

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We report the photorefractive properties of a new polymer mixture composed of 40 wt. % benzaldehyde-diphenyl hydrazone dissolved in Bisphenol A 4,4'-nitroaminostilbene. The polymer has a response time of 0.11±0.02 sec at 1 W/cm2, an overall photorefractive sensitivity (index change per unit absorbed energy density) of 1.8±0.5 × 10−6 cm3/J.
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Reports on the topic "Hydrazoic"

1

Hallman, D. F. Hydrazoic Acid Controls and Risks When Processing Plutonium Solutions in HB-Line Phase II. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/783008.

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HALLMAN, DONALD. HYDRAZOIC ACID CONTROLS AND RISKS WHEN PROCESSING NEPTUNIUM SOLUTIONS IN HB-LINE PHASE II. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/882776.

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HALLMAN, DONALD. HYDRAZOIC ACID CONTROLS AND RISKS WHEN PROCESSING NEPTUNIUM SOLUTIONS IN HB-LINE PHASE II. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/882777.

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