Relevant bibliographies by topics / Cyanoacetohydrazide

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Cyanoacetohydrazide'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Cyanoacetohydrazide"

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Jadeja, Juvansinh, Mayank Mamtora, Mitesh B. Gondaliya, Rohit Manawar, and Manish K. Shah. "Synthesis, Spectral Analysis and Evolution of Antimicrobial Activity of Schiff Base of Cyanoacetohydrazide." International Letters of Chemistry, Physics and Astronomy 52 (June 2015): 100–110. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.52.100.

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In search of some antimicrobial agents, synthesis of some Schiff base of cyanoacetohydrazide derivatives has been reported. The structures of all the synthesized compounds were established on the bases of various spectroscopic methods. All Schiff base were screened for antimicrobial activity. cyanoacetohydrazide were found to possess better antimicrobial potential.
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Pomes Hernandez, R., A. Gómez González, A. Rosado Pérez, B. M. Nápoles Frías, R. A. Toscano, and J. Quincoces Suárez. "N'-[Bis(methylthio)methylene]cyanoacetohydrazide." Acta Crystallographica Section C Crystal Structure Communications 52, no. 11 (1996): 2941–42. http://dx.doi.org/10.1107/s0108270196007147.

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Atta-Allah, Saad R., Wael S. I. Abou-Elmagd, Kamal A. A. Kandeel, Magdy M. Hemdan, David S. A. Haneen, and Ahmed S. A. Youssef. "Synthesis and Antimicrobial Activity Evaluation of Some Novel Hydrazone, Pyrazolone, Chromenone, 2-Pyridone and 2-Pyrone Derivatives." Journal of Chemical Research 41, no. 11 (2017): 617–23. http://dx.doi.org/10.3184/174751917x15065183733150.

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A cyanoacetohydrazide derivative underwent a series of reactions with different nucleophilic reagents, such as hydrazine hydrate, p-chlorobenzaldehyde and salicylaldehyde, to give the condensation products. In addition, an arylidene malononitrile was reacted with different nitrogen nucleophiles, such as hydrazine hydrate, thiocarbohydrazide and cyanoacetohydrazide, to afford the hydrazine, hydrazone and pyridin-2-one derivatives, respectively. Furthermore, a pyridin-2-one derivative was reacted with different carbon electrophiles, such as carbon disulfide, p-chlorobenzaldehyde and acetic anhyd
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4

Elkholy, Said S., Khalid D. Khalil, and Maher Zaki Elsabee. "Grafting of acryloyl cyanoacetohydrazide onto chitosan." Journal of Polymer Research 18, no. 3 (2010): 459–67. http://dx.doi.org/10.1007/s10965-010-9437-x.

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Hosseini, Hajar, and Mohammad Bayat. "Synthesis of 5-amino-N′-(9H-fluoren-9-ylidene)-8-nitro-7-aryl-1,2,3,7-tetrahydroimidazo[1,2-a]pyridine-6-carbohydrazide derivatives based on heterocyclic ketene aminals." RSC Advances 8, no. 72 (2018): 41218–25. http://dx.doi.org/10.1039/c8ra09308c.

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A new class of tetrahydroimidazo[1,2-a]pyridine derivatives has been successfully prepared via a five-component domino reaction using cyanoacetohydrazide, 9-fluorenone, aromatic aldehydes, 1,1-bis(methylthio)-2-nitroethene and ethylenediamine in ethanol at reflux.
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El-Sharief, Marwa A. M. Sh, Samir Y. Abbas, Medhat A. Zahran, Yehia A. Mohamed, Ahmed Ragab, and Yousry A. Ammar. "New 1,3-diaryl-5-thioxo-imidazolidin-2,4-dione derivatives: synthesis, reactions and evaluation of antibacterial and antifungal activities." Zeitschrift für Naturforschung B 71, no. 8 (2016): 875–81. http://dx.doi.org/10.1515/znb-2016-0054.

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AbstractNew cyanothioformamide derivative 1 was prepared by treatment of 3,5-dichlorophenyl isothiocyanate with potassium cyanide at room temperature. Cycloaddition of cyanothioformamide 1 with phenyl isocyanate as electrophile furnished the corresponding imidazolidine 2. Imine hydrolysis of 2 with ethanolic HCl produced the corresponding 4-thioxo-2,5-imidazolidinedione 3. This compound was used as key synthon for the preparation of a wide variety of new substituted imidazole compounds. Condensation of 3 with different types of hydrazine derivatives furnished new series of hydrazone 4a, b, thi
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7

Martins, Marcos A. P., Dayse N. Moreira, Clarissa P. Frizzo, Kelvis Longhi, Nilo Zanatta та Helio G. Bonacorso. "Reaction of β-alkoxyvinyl halomethyl ketones with cyanoacetohydrazide". Journal of the Brazilian Chemical Society 19, № 7 (2008): 1361–68. http://dx.doi.org/10.1590/s0103-50532008000700019.

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8

Nilov, D. B., and V. G. Granik. "Study of reactions of lactim ethers with cyanoacetohydrazide." Russian Chemical Bulletin 55, no. 9 (2006): 1636–41. http://dx.doi.org/10.1007/s11172-006-0466-x.

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9

Mekheimer, Ramadan A., and Rafat M. Shaker. "Synthesis and Reactivity of 3-Alkylthio-5-cyanomethyl-4-phenyl-1,2,4-triazoles." Journal of Chemical Research 23, no. 2 (1999): 76–77. http://dx.doi.org/10.1177/174751989902300205.

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Phenyl isothiocyanate reacts with 2-cyanoacetohydrazide (1) to yield the corresponding 1-cyanoacetyl-4-phenylthiosemicarbazide (3), via acid hydrolysis of the intermediate 2 whereas cyclization of 3 gave the 1,2,4-triazoles 4, 1,3,4-thiadiazoles 7 and 1,3,4-thiadiazine-5-ones 9; compound 4a was reacted with phenyl isothiocyanate, dicyandiamide, sulfanylacetic acid and benzaldehyde to afford 11, 13, 14 and 15, respectively.
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10

Al-Awadi, Nouria A., and Maher Z. Elsabee. "Pyrolysis of N-acryloyl, N′cyanoacetohydrazide and its polymer." Polymer Degradation and Stability 50, no. 3 (1995): 319–22. http://dx.doi.org/10.1016/0141-3910(95)00140-9.

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Dissertations / Theses on the topic "Cyanoacetohydrazide"

1

Moreira, Dayse das Neves. "Reações de ciclocondensação de cianoacetoidrazida com enonas halometil-substituídas." Universidade Federal de Santa Maria, 2008. http://repositorio.ufsm.br/handle/1/10429.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>The synthesis of thirteen 3-(R1), 4-(R2) and 5-(R3)-substituted 1-cyanoacetyl-5-hydroxy-4,5-dihydro-1H-pyrazoles from the cyclocondensation reaction of 4-alkoxy-3-alken-2-ones [R3C(O)C(R2)=C(R1)(OR), where R3 = CF3, CCl3, CHCl2, CO2Et; R2 = H, Me; R1 = H, Me, Et, Pr, Pentyl, c-Hexyl, Ph, and R = Me, Et] with cyanoacetohydrazide is reported. This reaction was carried out in different methodologies, firstly using water like solvent and following with ionic liquid ([BMIM]BF4). The results showed that when the ionic liquid was used as
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