Relevant bibliographies by topics / Bromothiazolo

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  2. Conference papers

Academic literature on the topic 'Bromothiazolo'

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

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Journal articles on the topic "Bromothiazolo"

1

Rangnekar, D. W., and N. D. Sonawane. "Synthesis and application of 2-styryl-6(7)-bromothiazolo[4,5-b]quinoxaline based fluorescent dye chromophores: Part 2." Dyes and Pigments 45, no. 2 (2000): 87–96. http://dx.doi.org/10.1016/s0143-7208(00)00006-1.

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2

Hwang, Hee-Jong, Young-Jin Son, Dahyun Kim, et al. "Diversity-oriented routes to thiopeptide antibiotics: total synthesis and biological evaluation of micrococcin P2." Organic & Biomolecular Chemistry 20, no. 9 (2022): 1893–99. http://dx.doi.org/10.1039/d1ob02145a.

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3

Li, Jiang-Tao, Jing-Kang Wang, and Li-Na Zhou. "N-(2-Bromothiazol-5-ylmethyl)phthalimide." Acta Crystallographica Section E Structure Reports Online 62, no. 6 (2006): o2327—o2328. http://dx.doi.org/10.1107/s1600536806017260.

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4

Lamberth, Clemens, Sarah Sulzer-Mosse, and Peter Kubizna. "Synthesis of Ring-Opened Analogues of Oxysterol-Binding Protein-Inhibiting Piperidinyl-thiazole Fungicides." Synlett 28, no. 17 (2017): 2277–80. http://dx.doi.org/10.1055/s-0036-1588473.

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Novel aminoethyl-, aminopropyl-, and aminobutyl-substituted thiazole-4-carboxamides have been prepared which are ring-opened analogues of piperidinyl-thiazole fungicides. Depending of the chain length, completely different synthetic approaches had to be chosen which vary from a Sonogashira coupling with a 2-bromothiazole derivative to a thiazole ring construction from different β- and δ-amino acids.
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Katritzky, Alan R., Kathleen S. Laurenzo, and Douglas I. Relyea. "The preparation and fungicidal activity of a series of thiazolyl- and isothiazoiyl-diarylcarbinols." Canadian Journal of Chemistry 66, no. 7 (1988): 1617–24. http://dx.doi.org/10.1139/v88-262.

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(Isothiazol-5-yl)diarylcarbinols were prepared from 5-lithioisothiazole. (Thiazol-5-yl)diarylcarbinols were obtained via 5-lithio-2-bromothiazole or 5-lithio-2-trimethylsilylthiazole with subsequent removal of the 2-substituent. Corresponding 2-aminothiazol-5-ylcarbinols were made by protecting 2-aminothiazole as its bis(trimethylsilyl) derivative. Biological activities were compared to the calculated electron densities at the heterocyclic N-atoms.
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6

Ji, Chang, and Dennis G. Peters. "Electrochemical reduction of 2-bromothiazole at carbon cathodes in acetonitrile." Journal of Electroanalytical Chemistry 455, no. 1-2 (1998): 147–52. http://dx.doi.org/10.1016/s0022-0728(98)00158-2.

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7

Obushak, N. D., V. S. Matiichuk, N. I. Ganushchak, and R. L. Martyak. "Synthesis of 4-amino-5-arylmethyl-2-bromothiazoles." Chemistry of Heterocyclic Compounds 33, no. 8 (1997): 1000. http://dx.doi.org/10.1007/bf02253182.

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8

Ghabbour, Hazem A. "Crystal structure of ethyl 2-amino-5-bromothiazole-4-carboxylate, C6H7BrN2O2S." Zeitschrift für Kristallographie - New Crystal Structures 231, no. 2 (2016): 629–30. http://dx.doi.org/10.1515/ncrs-2015-0216.

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9

da Silva, Luiz Everson, Antonio Carlos Joussef, Carla Regina Andrighetti-Fröhner, Ricardo José Nunes, and Adailton José Bortoluzzi. "5-(5-Bromothiazol-2-ylaminomethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione." Acta Crystallographica Section E Structure Reports Online 62, no. 3 (2006): o1062—o1063. http://dx.doi.org/10.1107/s1600536806005307.

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10

Aitken, Kati M., R. Alan Aitken, Callum I. MacGregor, Mohamed D. M. Traore, and Alexandra M. Z. Slawin. "The X-ray Structures of 2,4-Dibromothiazole and 2,4-Diacetyl-5-bromothiazole." Journal of Chemical Crystallography 45, no. 10-12 (2015): 461–65. http://dx.doi.org/10.1007/s10870-015-0615-x.

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Conference papers on the topic "Bromothiazolo"

1

Ali, Asam Hussein, Aseel Farhan Abdullah, Mohammed Mahdi Mohammed, Raheem A. H. Al-Uqaily, and Subhi A. H. Al-Bayaty. "The use of an organic compound (ethyl-2-bromothiazole-4-carboxylate) as an inhibitor to reduce the corrosion of copper in acidic media." In TRANSPORT, ECOLOGY, SUSTAINABLE DEVELOPMENT: EKO VARNA 2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0191596.

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