Academic literature on the topic 'Trifluoromethylated pyrazoline synthesis'

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Journal articles on the topic "Trifluoromethylated pyrazoline synthesis"

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Yuan, Fangchong, Wenwen Duan, Zeyu Li, et al. "One-Pot Synthesis of Trifluoromethylated Pyrazol-4-yl-pyrrole-2,5-dione Derivatives." Synthesis 51, no. 17 (2019): 3345–55. http://dx.doi.org/10.1055/s-0037-1611837.

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Efficient and convenient one-pot, three-component reactions of pyrrolidone, aromatic aldehydes and 1-phenyl-3-trifluoromethyl-5-pyrazolone afforded highly functionalized trifluoromethylated pyrazol-4-ylpyrrole-2,5-dione derivatives in good yields. The effect of solvents on the reaction efficiency and yield was briefly investigated. The structures of products were determined by spectral methods and X-ray diffraction analysis. The latter showed that the products formed have a strong intramolecular hydrogen bond, which made them particularly stable and the corresponding annulated products were no
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Wang, Yuxiang, Ke-Hu Wang, Yingpeng Su, et al. "Cascade Oxidation/Halogenoaminocyclization Reaction of Trifluoromethylated HomoallylicN-Acylhydrazines: Metal-free Synthesis of CF3-Substituted Pyrazolines." Journal of Organic Chemistry 83, no. 2 (2018): 939–50. http://dx.doi.org/10.1021/acs.joc.7b02934.

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Dai, Hong, Hai-Bo Yu, Jian-Bing Liu, et al. "Synthesis and bioactivities of novel trifluoromethylated pyrazole oxime ether derivatives containing a pyridyl moiety." Arkivoc 2009, no. 7 (2009): 126–42. http://dx.doi.org/10.3998/ark.5550190.0010.713.

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Wu, Yongming, Haibo Xie, Jiangtao Zhu, Zixian Chen та Shan Li. "Reaction of a Trifluoromethylated N-Monosubstituted Hydrazone with α,β-Ethenyl Ketones: A Novel Synthesis of Substituted Pyrazolidines and Pyrazolines". Synthesis 2011, № 17 (2011): 2767–74. http://dx.doi.org/10.1055/s-0030-1260127.

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Xie, Haibo, Jiangtao Zhu, Zixian Chen, Shan Li та Yongming Wu. "ChemInform Abstract: Reaction of a Trifluoromethylated N-Monosubstituted Hydrazone with α,β-Ethenyl Ketones: A Novel Synthesis of Substituted Pyrazolidines and Pyrazolines." ChemInform 43, № 3 (2011): no. http://dx.doi.org/10.1002/chin.201203108.

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Kalaria, Piyush N., Shailesh P. Satasia, and Dipak K. Raval. "l-Proline promoted green and regioselective synthesis of a novel pyrazole based trifluoromethylated fused thiazolopyran scaffold and its biological evaluation." RSC Advances 4, no. 61 (2014): 32353. http://dx.doi.org/10.1039/c4ra04283b.

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Kalaria, Piyush N., Shailesh P. Satasia, and Dipak K. Raval. "ChemInform Abstract: L-Proline Promoted Green and Regioselective Synthesis of a Novel Pyrazole Based Trifluoromethylated Fused Thiazolopyran Scaffold and Its Biological Evaluation." ChemInform 46, no. 8 (2015): no. http://dx.doi.org/10.1002/chin.201508208.

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Karnakar, K., K. Ramesh, K. Harsha Vardhan Reddy, B. S. P. Anil Kumar, Jagadeesh Babu Nanubonula, and Y. V. D. Nageswar. "A novel one pot four-component reaction for the efficient synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-3′-carboxylate and trifluoromethylated spiro[indole-3,4′-pyrano[2,3-c]pyrazole] derivatives using recyclable PEG-400." New Journal of Chemistry 39, no. 11 (2015): 8978–83. http://dx.doi.org/10.1039/c5nj01448d.

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Karnakar, K., K. Ramesh, K. Harsha Vardhan Reddy, B. S. P. Anil Kumar, Jagadeesh Babu Nanubonula, and Y. V. D. Nageswar. "ChemInform Abstract: A Novel One Pot Four-Component Reaction for the Efficient Synthesis of Spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-3′-carboxylate and Trifluoromethylated Spiro[indole-3,4′-pyrano[2,3-c]pyrazole] Derivatives Using Recyclable PEG-400." ChemInform 47, no. 10 (2016): no. http://dx.doi.org/10.1002/chin.201610104.

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Wei, Lan, Shiteng Ding, Mingqing Liu, Zongxiang Yu та Yuanjing Xiao. "Synthesis of Trifluoromethylated Pyrazolidines, Pyrazolines and Pyrazoles via Divergent Reaction of β-CF3-1,3-Enynes with Hydrazines". Organic Letters, 20 вересня 2021. http://dx.doi.org/10.1021/acs.orglett.1c02646.

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Dissertations / Theses on the topic "Trifluoromethylated pyrazoline synthesis"

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Diercxsens, Nicolas. "Synthèse d’amidines et de composés trifluorométhylés par le biais de molécules hautement réactives." Thèse, 2017. http://hdl.handle.net/1866/20038.

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