Relevant bibliographies by topics / Bromobenzamide

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Bromobenzamide'

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

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Journal articles on the topic "Bromobenzamide"

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Xing, Zhi-Tao, Hai-Bo Wang, Jun Yin, Wen-Yuan Wu, and Feng Han. "4-Bromobenzamide oxime." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2236—o2237. http://dx.doi.org/10.1107/s1600536807015863.

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Cavalheiro, Valéria Machado Siqueira, Sabrina Madruga Nobre, and Felipe Kessler. "Correction: Study of the dual functional behaviour of 1,2-bis(4-bromobenzamide)benzene by synchronous fluorescence spectroscopy." New Journal of Chemistry 43, no. 24 (2019): 9740. http://dx.doi.org/10.1039/c9nj90078k.

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Correction for ‘Study of the dual functional behaviour of 1,2-bis(4-bromobenzamide)benzene by synchronous fluorescence spectroscopy’ by Valéria Machado Siqueira Cavalheiro et al., New J. Chem., 2019, 43, 7162–7168.
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Cavalheiro, Valéria Machado Siqueira, Sabrina Madruga Nobre, and Felipe Kessler. "Study of the dual functional behaviour of 1,2-bis(4-bromobenzamide)benzene by synchronous fluorescence spectroscopy." New Journal of Chemistry 43, no. 18 (2019): 7162–68. http://dx.doi.org/10.1039/c8nj06066e.

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This study presents the dual functionality of 1,2-bis(4-bromobenzamide)benzene, where depending on the stoichiometric conditions, temperature and reaction time, the compound may act as a PdCl<sub>2</sub> ligand or as one of the reactants of the Suzuki coupling reaction.
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B., THIMME GOWDA, JAGAN MOHANA RAO P., and DARLIN QUINE S. "Kinetics and Mechanism of Bromination of Phenol and Substituted Phenols by N-Bromobenzamide in Aquo-acetic Acid Medium." Journal of Indian Chemical Society Vol. 69, Dec 1992 (1992): 830–34. https://doi.org/10.5281/zenodo.6116677.

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Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangothri-574 199 <em>Manuscript received 2 December 1991, revised 24 August 1992, accepted 24 September 1992</em> Kinetics of bromination of phenol and substituted phenols by <em>N</em>-bromobenzamide <em>have </em>been studied in aquo-acetic acid (1 : 1, v/v) medium. The rates of bromination show first order kinetics in [NBB], fractional order in [phenols] and zero order in [H<sup>+</sup>]. The rate slightly decreases with the addition of the reduced product of the oxidant, while the increase in aceti
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Y., Dominic Ravichandran, Kishor Rachna, Hariharasubramanian A., Mohana Priya K., and S. Khora Samanta. "Synthesis and characterization of N-substituted benzimidazole derivatives and study of their antibacterial and antifungal activity." Journal of Indian Chemical Society Vol. 92, Jun 2015 (2015): 915–17. https://doi.org/10.5281/zenodo.5637656.

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Organic Chemistry Division, School of Advanced Sciences, VIT University, Vellore-632 014, Tamilnadu, India <em>E-mail </em>: dominic.y@vit.ac.in Medical Biotechnology Division, School of Bioscience and Technology, VIT University, Vellore-632 014, Tamilnadu, India N-(4-(1<em>H</em>-Benzo[d]imidazol-1-yl)phenyl)-3-nitrobenzamide, N-(4-(1<em>H</em>-benzo[d]imidazol-1-yl)phenyl)-4- chlorobenzamide, 4-(1<em>H</em>-benzo[d]imidazol-1-yl)benzenamine and N-(4-(1<em>H</em>-benzo[<em>d</em>]imidazol-1-yl)phenyl)-4-bromobenzamide were synthesized and characterized by IR and NMR techniques. These N-substi
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Hu, Rong-Hua, Yan Sui, Ji-Wu Wen, Zhi-Gang Luo, and Long-Jin Zhong. "A New Type of Organic Ferroelectric N-Dehydroabietyl-4-bromobenzamide." Asian Journal of Chemistry 27, no. 7 (2015): 2627–29. http://dx.doi.org/10.14233/ajchem.2015.18628.

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Liu, Zibin, Li-Yan Zeng, Chao Li, et al. "“On-Water” Synthesis of Quinazolinones and Dihydroquinazolinones Starting from o-Bromobenzonitrile." Molecules 23, no. 9 (2018): 2325. http://dx.doi.org/10.3390/molecules23092325.

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A versatile and practical “on-water” protocol was newly developed to synthesize quinazolinones using o-bromobenzonitrile as a novel starting material. Studies have found that air as well as water plays an important role in synthesis of quinazolinones. Further investigation indicated that dihydroquinazolinones can be prepared with this protocol under the protection of N2. The protocol can be extended to other substrates and various quinazolinones and dihydroquinazolinones were obtained. o-Bromobenzamide, o-aminobenzonitrile, and o-aminobenzamide were also evaluated as starting materials, and th
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8

Huang, Yu-Ying, Hui-Chang Lin, Kaung-Min Cheng, et al. "Efficient di-bromination of 5-pyrazolones and 5-hydroxypyrazoles by N-bromobenzamide." Tetrahedron 65, no. 46 (2009): 9592–97. http://dx.doi.org/10.1016/j.tet.2009.09.055.

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9

Chowdhury, Kakuli, and Kalyan K. Banerji. "Kinetics and mechanism of the oxidation of organic sulfides by N-bromobenzamide." Journal of Organic Chemistry 55, no. 19 (1990): 5391–93. http://dx.doi.org/10.1021/jo00306a017.

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Banerji, Kalyan K. "Kinetics and mechanism of the oxidation of substituted benzaldehydes by N-bromobenzamide." Journal of Organic Chemistry 51, no. 25 (1986): 4764–67. http://dx.doi.org/10.1021/jo00375a004.

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Dissertations / Theses on the topic "Bromobenzamide"

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Donati, Ludovic. "L' unité ortho-bromobenzamide : étude de la réactivité en couplage organopalladié et application à la synthèse de pyridopyrroloisoquinolones et de phénanthridinones à potentialité thérapeutique." Paris 5, 2010. http://www.theses.fr/2010PA05P636.

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Ce projet se place dans le cadre de la préparation de nouveaux composés antitumoraux, analogues de la fagaronine et de la nitidine, alcaloïdes naturels inhibiteurs de la topoisomérase I. Les nouvelles structures envisagées sont de type pyridopyrroloisoquinolones et pyridopyrroloquinolones. Les stratégies de synthèse mises en oeuvre ont conduit à la formation de nouveaux produits possédant une structure tétracyclique ou tricyclique inattendues. Afin de comprendre la réactivité du motif orthobromobenzamide en pallado-catalyse, la formation des dérivés tricycliques a fait l'objet d'une étude méca
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Huang, Yu-Ying, and 黃俞穎. "Efficient Bromination of 5-Pyrazolones and 5-Hydroxypyrazoles by N-Bromobenzamide and Dibromoisocyanuric acid." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/56727404362986312087.

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碩士<br>中國醫藥大學<br>藥物化學研究所碩士班<br>97<br>An efficient and convenient method for the bromination of pyrazolones and 5-hydroxypyrazoles was developed by used of N-bromobenzamide or dibromoisocyanuric acid in THF at room temperature. A safe bromination has been developed for pyrazolones and 5-hydroxypyrazoles to give the corresponding di-brominated pyrazolones in excellent yields (≥ 90%).
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Book chapters on the topic "Bromobenzamide"

1

lvarez, M., and J. A. Joule. "From 2-Bromobenzamide." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01419.

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You might also be interested in the extended bibliographies on the topic 'Bromobenzamide' for particular source types:
Journal articles
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