Academic literature on the topic 'Phenyl hydrazine method'
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Journal articles on the topic "Phenyl hydrazine method"
Ananthi, Vadamalai, Kaliyaraj Rajalakshmi, Inbasekaran Muthuvel, and Ganesamoorthy Thirunarayanan. "Solid acidic FeCl3/Bentonite catalyzed solvent-free condensation: Synthesis, spectral studies and antimicrobial activities of some aryl hydrazine Schiff’s bases." Annales Universitatis Mariae Curie-Sklodowska, sectio AA – Chemia 71, no. 2 (2017): 127. http://dx.doi.org/10.17951/aa.2016.71.2.127.
Full textKaur, 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.
Full textGHAMMAMY, SHAHRIAR, and SAJJAD SEDAGHAT. "Determination and Characterization of New Palladium Complexes and Study of their Properties." Material Science Research India 9, no. 2 (2012): 223–26. http://dx.doi.org/10.13005/msri/090207.
Full textRaut, Santosh, Bharat Dhotre, Atul Tidke, and Mohammad Arif Pathan. "An Operationally Simple and Efficient Synthesis of 7-Benzylidene-substitutedphenyl- 3,3a,4,5,6,7-hexahydro-2H-indazole by Grinding Method." Current Organic Synthesis 17, no. 4 (2020): 313–21. http://dx.doi.org/10.2174/1570179417666200406142118.
Full textAli, M. M., M. Jesmin, S. M. A. Salam, J. A. Khanam, M. F. Islam, and M. N. Islam. "Pesticidal Activities of Some Schiff Bases Derived from Benzoin, Salicylaldehyde, Aminophenol and 2,4 Dinitrophenyl Hydrazine." Journal of Scientific Research 1, no. 3 (2009): 641–46. http://dx.doi.org/10.3329/jsr.v1i3.2585.
Full textBhandarkar, Subodh, and Bhavana Khobragade. "Synthesis and Biological Study of 2-( 5-aryl-4,5-dihydro-1-substituted-pyrazol-3-yl )-Substituted-Naphthalene-1-Ol." Advanced Materials Research 1110 (June 2015): 306–10. http://dx.doi.org/10.4028/www.scientific.net/amr.1110.306.
Full text.Gowd, V. S. "Facile and Multicomponent Synthesis of Amino Pyrazole employed by Mg (NO3)2 As Catalyst." INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT 09, no. 05 (2025): 1–9. https://doi.org/10.55041/ijsrem48648.
Full textGiribabu, G., and Dr KRISHNARAO. "One Pot Multicomponent Synthesis of Amino Pyrazole Promoted by Imidazole and Bioevluation." INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT 09, no. 04 (2025): 1–9. https://doi.org/10.55041/ijsrem44605.
Full textKomal, Savaliya, and S. Patel Pankaj. "Synthesis and Biological evaluation Of Some New Benzoyl Pyrazole Derivatives bearing a 6,8-Dibromo-2-methylquinazolin-4-one Moiety." Der Pharma Chemica 14, no. 2 (2022): 6. https://doi.org/10.4172/0975-413X.14.2.1-5.
Full textSavaliya, Komal, and S. Patel Pankaj. "Synthesis and Biological evaluation Of Some New Benzoyl Pyrazole Derivatives bearing a 6,8-Dibromo-2-methylquinazolin-4-one Moiety." Der Pharma Chemica 14, no. 2 (2022): 6. https://doi.org/10.5281/zenodo.13353950.
Full textDissertations / Theses on the topic "Phenyl hydrazine method"
Haelters, Jean-Pierre. "Synthèse de dérivés phosphono-indoliques-benzofuranniques et -pyrroliques à partir d'hydrazones phosphonates." Brest, 1987. http://www.theses.fr/1987BRES2002.
Full textBook chapters on the topic "Phenyl hydrazine method"
Ghate, Manjunath, and Manohar V. Kulkarni. "Unusual reaction of 4-bromomethyl coumarin with hydrazine hydrate and phenyl hydrazine in ethanol and acetic acid medium: and New method of synthesis of 3-oxo- 4-benzopyridazine." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50151-9.
Full textConference papers on the topic "Phenyl hydrazine method"
Popusoi, Ana, Nicanor Barba, and Aurelian Gulea. "Synthesis of 1,3-Phenyl(Pyridyl)propenones with thiosemicarbazidic groups." 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.ab03.
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