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Relevant bibliographies by topics / Imidazole-2-thiones

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Journal articles

Academic literature on the topic 'Imidazole-2-thiones'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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Journal articles on the topic "Imidazole-2-thiones"

1

Koner, Abhishek, Spencer C. Serin, Gregor Schnakenburg, Brian O. Patrick, Derek P. Gates, and Rainer Streubel. "Exploring the chemistry of backbone amino(chloro)phosphanyl-substituted imidazole-2-thiones." Dalton Transactions 46, no. 31 (2017): 10504–14. http://dx.doi.org/10.1039/c7dt01859b.

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2

Majhi, Paresh Kumar, Gregor Schnakenburg, Anthony J. Arduengo, and Rainer Streubel. "Synthesis and Oxidative Desulfurization of PV-Functionalized Imidazole-2-thiones: Easy Access to P-Functional Ionic Liquids." Australian Journal of Chemistry 68, no. 8 (2015): 1282. http://dx.doi.org/10.1071/ch14726.

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Selective synthesis of 4-phosphanylated imidazole-2-thiones 2d, 3a,b(b′),c(c′),d were achieved using a backbone lithiation and phosphanylation reaction protocol. The 4-phosphanylated-imidazole-2-thiones 3b(b′),c(c′) were subjected to a oxidation/phosphanylation/oxidation reaction sequence to access C4/5-bis(phosphanoyl)-substituted imidazole-2-thiones 7b,c. Oxidative desulfurization of phosphanylated imidazole-2-thiones 2d, 4a,d, and 7b,c with hydrogen peroxide afforded the first examples of room temperature imidazolium ionic liquids 8d, 9a,d, and 10b,c respectively, possessing backbone P-subs

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3

Koner, Abhishek, Gregor Pfeifer, Zsolt Kelemen, et al. "1,4-Diphosphinines from Imidazole-2-thiones." Angewandte Chemie International Edition 56, no. 31 (2017): 9231–35. http://dx.doi.org/10.1002/anie.201704070.

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4

Trzhtsinskaya, Bella V., and Nina D. Abramova. "Imidazole-2-Thiones: Synthesis, Structure, Properties." Sulfur reports 10, no. 4 (1991): 389–421. http://dx.doi.org/10.1080/01961779108048760.

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5

Po, Henry N., Zarila Shariff, Jeffrey A. Masse, Fillmore Freeman, and Monica C. Keindl-yu. "THERMODYNAMIC AND ELECTROCHEMICAL PROPERTIES OF IMIDAZOLE-2-THIOLS (IMIDAZOLE-2(3H)-THIONES)." Phosphorus, Sulfur, and Silicon and the Related Elements 63, no. 1-2 (1991): 1–12. http://dx.doi.org/10.1080/10426509108029421.

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6

Batanero, Belén. "Electrosynthesis of N-Substituted Imidazole-2-thiones." Synthesis 1999, no. 10 (1999): 1809–13. http://dx.doi.org/10.1055/s-1999-3585.

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7

Mlostoń, Grzegorz, Małgorzata Celeda, Marcin Jasiński, et al. "2-Unsubstituted Imidazole N-Oxides as Novel Precursors of Chiral 3-Alkoxyimidazol-2-ylidenes Derived from trans-1,2-Diaminocyclohexane and Other Chiral Amino Compounds." Molecules 24, no. 23 (2019): 4398. http://dx.doi.org/10.3390/molecules24234398.

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‘Desymmetrization’ of trans-1,2-diaminocyclohexane by treatment with α,ω-dihalogenated alkylation reagents leads to mono-NH2 derivatives (‘primary-tertiary diamines’). Upon reaction with formaldehyde, these products formed monomeric formaldimines. Subsequently, reactions of the formaldimines with α-hydroxyiminoketones led to the corresponding 2-unsubstituted imidazole N-oxide derivatives, which were used here as new substrates for the in situ generation of chiral imidazol-2-ylidenes. Upon O-selective benzylation, new chiral imidazolium salts were obtained, which were deprotonated by treatment

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8

TRZHTSINSKAYA, B. V., and N. D. ABRAMOVA. "ChemInform Abstract: Imidazole-2-thiones: Synthesis, Structure, Properties." ChemInform 22, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199151344.

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9

Abramov, N. D., and B. V. Trzhtsinskaya. "Structure and properties of imidazole-2-thiones (review)." Chemistry of Heterocyclic Compounds 24, no. 12 (1988): 1309–21. http://dx.doi.org/10.1007/bf00486668.

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10

Wang, Xi-Cun, Fang Wang, Zheng-Jun Quan, Man-Gang Wang, and Zheng Li. "An efficient and clean synthesis of 1-aroyl-3-aryl-4-substituted imidazole-2-thiones in water." Journal of Chemical Research 2005, no. 11 (2005): 689–90. http://dx.doi.org/10.3184/030823405774909423.

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Treatment 1-aryl-3-aroyl/benzofuroyl thioureas with α-bromo substituted carbonyl compounds in water affording 1-aroyl/benzofuroyl-3-aryl-4-substituted imidazole-2-thiones in excellent yields within short time.

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