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Relevant bibliographies by topics / Heteroatomic1,2,3-Tiazole derivatives

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Academic literature on the topic 'Heteroatomic1,2,3-Tiazole derivatives'

Author: Grafiati

Published: 6 September 2023

Last updated: 31 July 2025

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Journal articles on the topic "Heteroatomic1,2,3-Tiazole derivatives"

1

Dufresne, Stéphane, Thomas Skalski, and W. G. Skene. "Insights into the effect of ketylimine, aldimine, and vinylene group attachment and regiosubstitution on the fluorescence deactivation of fluorene." Canadian Journal of Chemistry 89, no. 2 (2011): 173–80. http://dx.doi.org/10.1139/v10-089.

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The spectroscopic and electrochemical properties of a 9-substituted fluorene ketylimine (3) were investigated and compared with those of its vinylene analogue (4) to determine the origins of the quenched fluorescence of these compounds. The predominate mode of singlet excited state deactivation of the heteroatomic fluorene was found to be internal conversion involving bond rotation. Meanwhile, its carbon counterpart was found to undergo deactivation preferentially by intersystem crossing to form its triplet, which was confirmed by laser flash photolysis. Both 3 and 4 quenched the fluorescence

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2

Nalibayeva, Arailym M., Sergey N. Adamovich, Amangul Bold, et al. "Chankanai Zeolite Modified with Heteroatomic Derivatives of 3-Aminopropyltriethoxysilane as an Effective Sorbent for Ag(I), Co(II)." Water 16, no. 23 (2024): 3416. http://dx.doi.org/10.3390/w16233416.

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Bis-N,N-(3-triethoxysilylpropyl)thiosemicarbazide 3 was obtained by the condensation of 3-aminopropyltriethoxysilane 1 with thiosemicarbazide 2. Ethyl ether N-[3-(triethoxysilyl)propyl]-b-alanine 5 was obtained by the interaction of an equimolar amount of aminopropyltriethoxysilane 1 and ethyl acrylate 4 (aza-Michael reaction). Synthesized functional organosilanes 3 and 5 were successfully immobilized on the surface of natural zeolite Z (Chankanai deposit, Kazakhstan). Compounds and materials have been studied by NMR and IR Fourier spectroscopy and X-ray diffraction analysis. The elemental com

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3

Zhang, Ming-Xing, and Guang-Jiu Zhao. "Heteroatomic Effects on Charge-Transfer Mobility of Dianthra[2,3-b:2′,3′-f]thieno[3,2-b]thiophene (DATT) and Its Derivatives." Journal of Physical Chemistry C 116, no. 36 (2012): 19197–202. http://dx.doi.org/10.1021/jp306311v.

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4

Dembitsky, V. M., G. A. Tolstikov та M. Srebnik. "Boranes in Organic Chemistry 1. α-Carbonylalkyl- and β-Oxyalkylboranes in Organic Synthesis". Eurasian Chemico-Technological Journal 4, № 2 (2017): 87. http://dx.doi.org/10.18321/ectj522.

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<p>This review is devoted to the synthesis of a-carbonylalkyl- and β-hydroxy-alkyl boranes and their use in organic synthesis. a-Carbonyl-alkylboranes include several heteroatomic compounds, in particular, [1.2.3]-diazaborinines, uracyl boronic acids, and [1.2.3.4]-diaza-diboretes. The latter type has been obtained by the ketene aminoborations. The reactions of halogenboranes with diazoesters and sulfur ylides resulting in formation of a-carbonyl alkylborates containing diazofunction or ylide structural fragment are described. Amino and halogen boration of acetylenic acid esters was also

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5

Chintawar, Chetan C., Ranjini Laskar, Debanjan Rana, et al. "Photoredox-catalysed amidyl radical insertion to bicyclo[1.1.0]butanes." Nature Catalysis, October 22, 2024. http://dx.doi.org/10.1038/s41929-024-01239-9.

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AbstractReplacing planar aromatic rings in drug molecules with C(sp3)-rich isosteric mimetics, such as bicyclo[n.1.1]alkanes, can significantly alter their physicochemical and pharmacokinetic properties, often leading to higher clinical success rates. However, unlike a benzene ring, the structurally rigid C(sp3)-rich isosteric mimetics of heteroaromatic rings are rare. Heterobicyclo[n.1.1]alkanes are promising in this regard, but the lack of modular synthetic methods has currently hindered their exploration. We envisioned that the strategic and selective insertion of different heteroatomic uni

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