Relevant bibliographies by topics / ORGANIC DERIVATIVES OF HYDRAZINE

Contents

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

Academic literature on the topic 'ORGANIC DERIVATIVES OF HYDRAZINE'

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

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Journal articles on the topic "ORGANIC DERIVATIVES OF HYDRAZINE"

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Kaur, Aneet Kamal, Renu Bala, Poonam Kumari, Sumit Sood, and Karan Singh. "Microwave Assisted Vilsmeier-Haack Reaction on Substituted Cyclohexanone Hydrazones: Synthesis of Novel 4,5,6,7-Tetrahydroindazole Derivatives." Letters in Organic Chemistry 16, no. 3 (2019): 170–75. http://dx.doi.org/10.2174/1570178615666180917101637.

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Vilsmeier-Haack reaction is one of the most important chemical reactions used for formylation of electron-rich arens. Even though Vilsmeier-Haack reaction was studied on a wide variety of hydrazones of enolizable ketones, literature lacks the examples of the use of 4-substituted cyclohexanones as a substrate. The cyclization potential of hydrazones of cyclic keto compounds is still interested topic of investigation. In the present study, the reaction of various hydrazines with 4-substituted cyclohexanones was proceeded and the resulted hydrazones in crude form were treated with Vilsmeier- Haac
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Sapkota, Kamal Raj, Shilpi Kumari, Zeba Alam, and Md Serajul Haque Faizi. "Synthesis, and Structural Characterization of (E)-1-(4-((2-(2,4-Dinitrophenyl) hydrazono) methyl)phenyl) piperidine: A Combined Spectroscopic and Computational Study." Bhairahawa Campus Journal 7, no. 1 (2024): 41–55. https://doi.org/10.3126/bhairahawacj.v7i1.79948.

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This study Hydrazine-based piperidine derivatives are widely recognized for their significant roles in pharmaceutical development and material science research. In this context, the present study aimed to synthesize a novel hydrazone derivative to explore its structural and electronic features. This study presents the synthesis and structural characterization of (E)-1-(4-((2-(2,4-Dinitrophenyl)hydrazono)methyl)phenyl)piperidine) (DHP). The compound was obtained through a condensation reaction between 4-(piperidin-1-yl) benzaldehyde and (2,4-dinitrophenyl) hydrazine, achieving an 88% yield. Its
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Wu, Shouting, Xi Liang, Fang Luo, et al. "Synthesis, Crystal Structure and Bioactivity of Phenazine-1-carboxylic Acylhydrazone Derivatives." Molecules 26, no. 17 (2021): 5320. http://dx.doi.org/10.3390/molecules26175320.

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A phenazine-1-carboxylic acid intermediate was synthesized from the reaction of aniline and 2-bromo-3-nitro-benzoic acid. It was then esterified and reacted with hydrazine hydrate to afford phenazine-1-carboxylic hydrazine. Finally, 10 new hydrazone compounds 3a–3j were obtained by the condensation reaction of phenazine-1-carboxylic acid hydrazide and the respective aldehyde-containing compound. The structures were characterized by 1H and 13C NMR spectroscopy, MS and single crystal X-ray diffraction. The antitumor activity of the target compounds in vitro (HeLa and A549) was determined by thia
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Jasril, E. Juwiyatri, S. N. Fauza, and N. Afriana. "Synthesis, in vitro Antioxidant Activity, and Toxicity Evaluation of Hydrazone Derivatives Naphthalene-1-ylmethylene hydrazine." Journal of Physics: Conference Series 2049, no. 1 (2021): 012050. http://dx.doi.org/10.1088/1742-6596/2049/1/012050.

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Abstract Hydrazone is a versatile organic compound that has a basic structure (-NHN=CH-) called the azomethine group. This structure is responsible for the physical and chemical of hydrazone, which makes this compound has variety bioactivities such as antioxidant, antitumor, and anticancer. In this work, two hydrazone derivatives from 1-naphthaldehyde and hydrazine (phenylhydrazine/hydrazine hydrate) have been synthesized under microwave irradiation. Their antioxidant activity and toxicity were evaluated by DPPH and BSLT method, respectively. Structures of the synthesized compounds were confir
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Gera, Ankur, Chander Mohan, and Sandeep Arora. "Synthesis of Phthaloylglycyl Hydrazide Derivatives: Selective Protection of Phthalimide Group from Hydrazinolysis." Current Organic Synthesis 15, no. 6 (2018): 839–45. http://dx.doi.org/10.2174/1570179415666180601083256.

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Background: N-phthalimide amino acid hydrazide is a class of compounds that have the potential therapeutic use. In general, hydrazinolysis of N-substituted amino acid(s) ester removes the ester group and yields the corresponding hydrazide. However, in case if N-substitution group is phthalimide, phthalimide group is cleaved and not the ester group. The resulted compound, therefore, is amino acid ester rather than Nphthalimide amino acid hydrazide. The above class of compounds, because of susceptibility of phthalimide group to hydrazinolysis, has previously been synthesized by a lengthy three-s
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Yehye, Wageeh, and Amit Nath. "Acid Hydrazide: A Potential Reagent for the Synthesis of Semicarbazones." Synthesis 50, no. 21 (2018): 4301–12. http://dx.doi.org/10.1055/s-0037-1609557.

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Complex semicarbazone derivatives were successfully synthesized from substituted semicarbazides in acidic ethanol upon heating in the presence of aldehyde. The reaction is functional group tolerant and chemoselective because no terminal hydrazine moiety is present in the substituted semicarbazides. Thus, functional groups such as esters and acetyls, which are prone to reaction with hydrazine, can also be used in this reaction because the terminal hydrazine moiety of the acid hydrazide was protected by aryl isocyanates in order to prepare substituted semicarbazides. In addition, neither of the
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Timperio, Anna Maria, Sara Rinalducci, and Lello Zolla. "Hydrazide derivatives produce active oxygen species as hydrazine." Bioorganic Chemistry 33, no. 6 (2005): 459–69. http://dx.doi.org/10.1016/j.bioorg.2005.09.001.

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El-Naggar, Mohamed, Abd El-Galil E. Amr, Ahmed A. Fayed, Elsayed A. Elsayed, Mohamed A. Al-Omar, and Mohamed M. Abdalla. "Potent Anti-Ovarian Cancer with Inhibitor Activities on Both Topoisomerase II and V600EBRAF of Synthesized Substituted Estrone Candidates." Molecules 24, no. 11 (2019): 2054. http://dx.doi.org/10.3390/molecules24112054.

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A series of 16-(α-alkoxyalkane)-17-hydrazino-estra-1(10),2,4-trien[17,16-c]-3-ol (3a–l) and estra-1(10),2,4-trien-[17,16-c]pyrazoline-3-ol derivatives (4a–d) were synthesized from corresponding arylidines 2a,b which was prepared from estrone 1 as starting material. Condensation of 1 with aldehydes gave the corresponding arylidine derivatives 2a,b which were treated with hydrazine derivatives in alcohols to give the corresponding derivatives 3a–l, respectively. Additionally, treatment of 2a,b with methyl- or phenylhydrazine in ethanolic potassium hydroxide afforded the corresponding N-substitut
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Kirilin, A. D., L. O. Belova, N. I. Kirilina, A. V. Petrogradsky, and N. L. Shembel. "PECULIARITIES OF ISOCYANATES INTERACTION WITH HYDRAZINE DERIVATIVES." Fine Chemical Technologies 13, no. 4 (2018): 39–49. http://dx.doi.org/10.32362/2410-6593-2018-13-4-39-49.

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The results of studies on chemical transformations of organic and organosilicon isocyanates in their interaction with hydrazine derivatives have been summarized in this review. It is shown that hydrazine and its derivatives including organosilicon compounds reacting with organic isocyanates form corresponding semicarbazides readily enough. The reaction conditions that effect the composition, structure and yield of the resulting target products are presented. A significant difference in the interaction of trimethylsilyl isocyanate with organic and organosilicon derivatives of hydrazine is demon
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Sepsey Für, Csilla, György Keglevich, and Hedvig Bölcskei. "Unexpected Formation of 4-aryl-1-(Propane-2-ylidenehydrazono)-2,3-diazaspiro[5.5]undec-3-ene by the Reaction of Pyridazinethiones Derivatives with Hydrazine." Molbank 2021, no. 3 (2021): M1243. http://dx.doi.org/10.3390/m1243.

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After making a new series of spiro[cycloalkane]pyridazinones with high Fsp3 character available, the new target was to synthesize derivatives comprising nitrogen-containing heterocycles, such as triazolo or tetrazolo rings. The corresponding thioxo derivatives (1a,b) seemed to be good starting materials for the synthesis of tetrazolo derivatives. The reaction of the pyridazinethiones (1a,b) with hydrazine surprisingly resulted in Schiff bases (3a,b) deriving from the reaction of hydrazones (2a,b) with acetone.
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Dissertations / Theses on the topic "ORGANIC DERIVATIVES OF HYDRAZINE"

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Yazici, Ceyda. "Synthesis Of 4-iodopyrazole Derivatives." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609750/index.pdf.

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Pyrazoles have been studied for over a century as an important class of heterocyclic compounds and continue to attract considerable interest due to the broad range of biological activities they possess. The electrophilic cyclization of the acetylenic hydrazones initiated by molecular iodine could provide new ways of synthesizing biologically active 4-iodopyrazole derivatives, which are important precursors for the synthesis of highly substituted pyrazole derivatives. For this reason, we investigated the synthesis of 4-iodopyrazole derivatives, such as 1-aryl- 5-alkyl/aryl-4-iodopyrazoles, star
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Mingle, David, and Abbas G. Dr Shilabin. "Synthesis, Characterization and Biological Evaluation of novel (S, E)-11-[2-(arylmethylene)hydrazono] pyrrolo [2,1-c] [1,4] benzodiazepine derivatives." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/asrf/2019/schedule/212.

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Pyrrolo [2,1-c] [1,4] benzodiazepine (PBD) is a class of natural products obtained from various actinomycetes which have both anti-tumor and antibiotic activities. They can bind to specific sequences of DNA that can trigger a biological response which is of pharmacological interest. PBD can also prevent cell division leading to death of the bacteria. This research focuses on the synthesis of novel 11-hydrazinyl PBD derivatives using a multi-step synthesis. PBD-dilactam was initially produced using isatoic anhydride and (L)-proline which was then converted to the PBD-thiolactam using Lawesson's
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Mingle, David. "Synthesis, Characterization and Biological Evaluation of Novel (S,E)-11-[2-(Arylmethylene) Hydrazono] Pyrrolo [2,1-c] [1,4] Benzodiazepine Derivatives." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/etd/3596.

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Pyrrolo [2,1-c] [1,4] benzodiazepine (PBD) is a class of natural products obtained from various actinomycetes which have both anti-tumor and antibiotic activities and can bind to specific sequences of DNA. PBD-dilactam was initially produced using isatoic anhydride and (L)-proline which was then converted to the PBD-thiolactam using Lawesson's reagent. Reaction of thiolactam with hydrazine in ethanol afforded PBD-11-hydrazinyl. Condensation of 11-hydrazinyl PBD with aldehydes possessing various substitutions was performed to obtain (S,E)-11-[2-(arylmethylene) hydrazono] pyrrolo [2,1-c] [1,4] b
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Aumand, Livia M. "A Studies towards the formation of asymmetric quaternary centres via radical allylation B Applications of chiral hydrazide organocatalysts to Diels-Alder, hydride reduction, and alpha-chlorination reactions C Studies directed towards the synthesis of potential HIV-1 reverse transcriptase inhibitors: 9-Alkylaryl TIBO derivatives." Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/26843.

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In part A, the attempts at synthesizing quaternary centres via radical reactions are described. Using tartrate acetals as chiral auxiliaries, tertiary bromides were submitted to radical allylation conditions in an effort to form 1,3-dicarbonyl compounds 27 possessing an asymmetric quaternary centre at C2.* Part B describes the synthesis of chiral hydrazide 129 and its ability to catalyze the Diels-Alder reaction is examined. The application of chiral hydrazides 131 to the organocatalytic hydride reduction of alpha,beta-unsaturated aldehydes and the alpha-chlorination of aldehydes is also recou
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Thompsett, David. "Hydrazine and carbazate complexes of chromium and manganese : their role in the catalytic decomposition of hydrazine." Thesis, University of Bath, 1987. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376340.

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Ghassemi, Hossein. "Synthesis and properties of novel polyimides utilizing hydrazine." Thesis, McGill University, 1994. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=28451.

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Hydrazine reacts with phthalic anhydride to give a mixture of cyclic hydrazide and N-aminophthalimide. However, the N-aminoimide is exclusively formed in high yield by the reaction of 1,8-naphthalic anhydride with hydrazine. N-aminoimides act as amines and react further with cyclic anhydrides to yield stable bisimides containing an N-N linkage. The syntheses of several bis(N-aminoimide)s from the corresponding bisanhydrides which contain the naphthalic anhydride moiety have been described. Novel high molecular weight polyimides have been synthesized by the reaction of these bis(N-aminoimide)s
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Chen, Lingyan. "CaSH (camphor sulfonyl hydrazine) and CSI (chiral sulfonimide) organocatalysis." HKBU Institutional Repository, 2010. http://repository.hkbu.edu.hk/etd_ra/1186.

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Bollan, Hilary Roberta. "The detection of hydrazine and related materials by ion mobility spectrometry." Thesis, Sheffield Hallam University, 1998. http://shura.shu.ac.uk/19366/.

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A technique known as ion mobility spectrometry (IMS), which has been under development for about thirty years, has been shown to be capable of detecting hydrazines at low concentrations but with interference from ammonia. Ammonia is usually present in hydrazine environments, as a breakdown product or a by-product of the human metabolism. This project was undertaken to investigate mechanical and chemical parameters for improved detection of these hydrazines in the presence of ammonia, and for the detection of nitrogen dioxide, by IMS. The subject areas investigated were compatibility of detecto
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Clavette, Christian. "Synthesis of Beta-Aminocarbonyl Compounds and Hydrazine Derivatives Using Amino- and Imino-Isocyanates." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32004.

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Over the past recent years, β-aminocarbonyls have been of great interest to medicinal chemists. As a practical method to obtain these moieties, alkene aminocarbonylation, accounting for the formation of a C-N and a C-C bond, has been the subject of limited research efforts (very specific intramolecular metal-catalyzed variants have been reported). Direct aminocarbonylation of alkenes constitutes a challenging and an important potential innovation in the synthesis of β-aminocarbonyls such as β-amino acids. The research efforts described in the present thesis have been primarily directed towards
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He, Hao. "Organocatalysis : hydrazine and sulfonimide as new functionalities in asymmetric organocatalysis." HKBU Institutional Repository, 2009. http://repository.hkbu.edu.hk/etd_ra/1104.

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Books on the topic "ORGANIC DERIVATIVES OF HYDRAZINE"

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Patil, K. C., and Tanu Mimani Rattan, eds. Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.

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Schmidt, Eckart W. Hydrazine and its derivatives: Preparation, properties, applications. 2nd ed. Wiley-Interscience, 2001.

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Cancer, International Agency for Research on. Re-evaluation of some organic chemicals, hydrazine and hydrogen peroxide. IARC, 1999.

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IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Re-evaluation of some organic chemicals, hydrazine and hydrogen peroxide. IARC, 1999.

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International Agency for Research on Cancer. Re-evaluation of some organic chemicals, hydrazine and hydrogen peroxide. IARC, 1999.

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International Agency for Research on Cancer. Re-evaluation of some organic chemicals, hydrazine and hydrogen peroxide. IARC, 1999.

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Dressler, Hans. Resorcinol: Its uses and derivatives. Plenum Press, 1994.

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United States. National Aeronautics and Space Administration, ed. Catalysts for the decomposition of hydrazine and its derivatives, and a method for its production. National Aeronautics and Space Administration, 1986.

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Patai, Saul, and Zvi Rappoport, eds. The Chemistry of Organic Derivatives of Gold and Silver. John Wiley & Sons, Ltd, 1999. http://dx.doi.org/10.1002/0470857196.

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Saul, Patai, and Rappoport Zvi, eds. The chemistry of organic derivatives of gold and silver. Wiley, 1999.

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Book chapters on the topic "ORGANIC DERIVATIVES OF HYDRAZINE"

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Aruna, Singanahally T., and K. C. Patil. "Hydrazine Salts." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch02.

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Patil, K. C., and Tanu Mimani Rattan. "Metal Hydrazine Carboxylates." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch04.

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Rattan, Tanu Mimani, and K. C. Patil. "Hydrazine and Its Inorganic Derivatives." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch01.

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Gajapathy, Dasaratharam, and Tanu Mimani Rattan. "Metal Hydrazines." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch03.

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Govindrajan, Subbiah, and Singanahally T. Aruna. "Hydrazinium Metal Complexes." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch05.

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Patil, K. C., and Tanu Mimani Rattan. "Applications of Inorganic Hydrazine Derivatives." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch06.

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Powis, Garth. "Triazine and Hydrazine Derivatives." In Cancer Management in Man. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1095-9_9.

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Vollhardt, Peter, and Neil Schore. "Carboxylic Acid Derivatives." In Organic Chemistry. Macmillan Learning, 2014. http://dx.doi.org/10.1007/978-1-319-19197-9_20.

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Tucker, William B. "Carboxylic Acid Derivatives." In Organic Chemistry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-21.

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Vollhardt, Peter, and Neil Schore. "Amines and Their Derivatives." In Organic Chemistry. Macmillan Learning, 2014. http://dx.doi.org/10.1007/978-1-319-19197-9_21.

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Conference papers on the topic "ORGANIC DERIVATIVES OF HYDRAZINE"

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Quraishi, M. A. "Lauric Hydrazide Derivatives: New Class of Volatile Corrosion Inhibitors." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02319.

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Abstract The protection of metals against corrosion by means of volatile compounds is the most progressive method of fighting metallic corrosion. These inhibitors are used to protect metallic articles and equipment during storage and transportation. In view of this we have synthesized six organic volatile corrosion inhibitors (VCIs) using Lauric hydrazide with various acids such as cinnamic acid, succinic acid, nitrobenzoic acid, phthalic acid and maleic acid and evaluated their inhibiting action on corrosion of mild steel, copper, brass, zinc and aluminium by weight loss and potentiodynamic p
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Jaffer, Arif, David Fulmer, and John Ensslen. "Recent Developments in Organic Oxygen Scavenger Technology." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06687.

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Abstract Oxygen scavenger performance is a major consideration in selecting the most favorable chemical treatment program for steam plants. In the last twenty-five years alternatives to hydrazine for oxygen removal in steam generating systems have been introduced. The paper reviews the current oxygen scavenger technology and presents the field evaluation data for three different organic oxygen scavengers in an industrial plant environment.
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Nazarova, P. V., V. I. Volk, and K. N. Dvoeglazov. "REAGENTLESS CATALYTIC OXIDATION OF ORGANIC HYDRAZINE DERIVATIVES AND Pu (III) BY MEANS OF NITRIC ACID." In RAD Conference. RAD Association, 2017. http://dx.doi.org/10.21175/radproc.2017.07.

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Karimatu, Hamza, Idris Abdullahi Yunusa, Muhammad Aliyu Musa, Hamza Asmau Nasiru, Hamza Sa’adatu Auwal, and Abdullahi Maryam. "Synthesis and In Vitro Antibacterial Studies of Two New Hydrazone Derivatives." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20138.

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Martins, Bruna Simões, Elisiane Frantz Heck, Caroline Raquel Bender, et al. "Synthesis of 1,3,4-oxadiazoles derivatives from -amino acids and acyl hydrazides using microwave irradiation." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0364-1.

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Guenter, Peter. "Novel High Nonlinearity Organic Crystals." In Nonlinear Optics: Materials, Fundamentals and Applications. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/nlo.1996.nwd.2.

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We will present the most recent results on the growth and characterization of novel high quality molecular crystals for nonlinear optics. These crystals are based on ionic or hydrogen bonding of new and known chromophores with large second-order hyperpolarizabilities. Detailed results of optical, electro-optical and nonlinear-optical properties of high quality and large size DAST crystals, of hydrazone derivatives and new co-crystals will be presented. It will be shown that optimized parallel alignment of chromophores as well as optimum structures for phase-matched frequency mixing have been r
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Bosshard, Christian, Pan Feng, Man Shing Wong, Martin Bösch, Urs Meier, and Peter Günter. "Thiophene Based Hydrazones: a New Class of Nonlinear Optical Molecular Crystals." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.thd.2.

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Crystalline solids are often regarded as the best choice of material form for practical use as optical frequency converters because of the excellent long-term orientational stability and extremely high density of active components. Such materials can be combined with inexpensive diode lasers for optic parametric generation of a broad range of optical frequencies [1, 2]. We here report on our on-going efforts in the development of novel and highly efficient second-order nonlinear optical crystalline materials for frequency conversion, based on the hydrazone derivatives 5-(methylthio)-thiophenec
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Meier, U., M. S. Wong, F. Pan, Ch Bosshard, P. Günter, and V. Gramlich. "Five-membered Heteroaromatic Hydrazone Derivatives for Second-Order Nonlinear Optics." In The European Conference on Lasers and Electro-Optics. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/cleo_europe.1996.ctuk72.

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In the past decades, there have been extensive research efforts in developing new highly efficient organic materials with large second order susceptibilities because of their potential applications in optical signal processing and frequency conversion. Molecules possessing a large firstorder molecular hyperpolarizability ß are an essential prerequisite for achieving large macroscopic susceptibilities χ(2). The molecular nonlinearity of the classical, nonlinear optically active molecule, which usually contains an electron donor and an electron acceptor connected by a π-conjugated core, can be e
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Zveaghinteva, Marina, Natalia Sucman, and Fliur Macaev. "Preparation of pyrazole class derivatives by heterocyclization of 1,2,4-triazolylethanones." In Conferința științifică națională cu participare internațională "Integrare prin cercetare și inovare", dedicată Zilei Internaționale a Științei pentru Pace și Dezvoltare. Moldova State University, 2025. https://doi.org/10.59295/spd2024n.93.

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In this work the peculiarities of the heterocyclization reaction of vinyltriazoles with the participation of hydrazine hydrate in ethanol and acetic acid are considered. Within the framework of this work it was found that the nature of the formed reaction products of the interaction of vinyltriazoles with hydrazine hydrate depends on the nature of the solvent. In boiling ethanol, 4,5-dihydro-1H-pyrazolinfunctionalized 1H-1,2,4-triazole is formed. Under acetic acid conditions, along with the formation of a pair of diastereomeric substances 4,5-dihydro-1H-pyrazoline series diastereomeric substan
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Liu, Li-Hung, Jhih-Syuan Teng, Yao-Jane Hsu, and Pen-Cheng Wang. "Preparation of carbon nanotube ink via organic hydrazine treatment." In 2014 9th International Microsystems, Packaging, Assembly and Circuits Technology Conference (IMPACT). IEEE, 2014. http://dx.doi.org/10.1109/impact.2014.7048444.

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Reports on the topic "ORGANIC DERIVATIVES OF HYDRAZINE"

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Clearfield, Abraham. Organic Derivatives of Layered Group (4) Phosphates. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada201080.

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Palilis, Leonidas C., Antti J. Maekinen, Hideyuki Murata, Manabu Uchida, and Zakya H. Kafafi. Efficient Molecular Organic Light-Emitting Diodes Based on Silole Derivatives. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada447724.

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Brel, Valery K. Development of the New Approaches in Designing of Fluoroorganic Derivatives Sulfur (Unsaturated, Heterocyclic, Aromatic Molecular Systems and Polyfunctional Organic Compounds). Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada447113.

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Belokonova, Nadezhda, Elena Ermishina, Natalya Kataeva, Natalia Naronova, and Kristina Golitsyna. E-learning course "Chemistry". SIB-Expertise, 2024. http://dx.doi.org/10.12731/er0770.29012024.

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Abstract:
The electronic training course ""Chemistry"" was created as an auxiliary resource to accompany the chemistry curriculum for the specialties of General Medicine, Pediatrics, and Dentistry. The purpose of studying the course is to form ideas about the structure and transformations of organic and inorganic substances that underlie life processes and influence these processes, in direct connection with the biological functions of these compounds. Course objectives: - formation of knowledge and skills about the basic laws of thermodynamics and bioenergy; about the structure and chemical properties
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