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Thematische Bibliographien / Dithioethers

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Konferenzberichte

Auswahl der wissenschaftlichen Literatur zum Thema „Dithioethers“

Autor: Grafiati

Veröffentlicht am 18. Mai 2024

Zuletzt aktualisiert am 31. Juli 2025

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Zeitschriftenartikel zum Thema "Dithioethers"

1

Furukawa, Naomichi, Hisashi Fujihara, and Akira Kawada. "Formation of Dithioether Diactions of Cyclic Dithioethers in Concentrated Sulfuric Acid." HETEROCYCLES 24, no. 1 (1986): 17. http://dx.doi.org/10.3987/r-1986-01-0017.

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2

Kundu, Samir, Babli Roy, and Basudeb Basu. "Silica: An efficient catalyst for one-pot regioselective synthesis of dithioethers." Beilstein Journal of Organic Chemistry 10 (January 7, 2014): 26–33. http://dx.doi.org/10.3762/bjoc.10.5.

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The development of a silica-promoted highly selective synthesis of 1,2 or 1,3-dithioethers via solvent-free one-pot tandem reactions of an allyl bromide with excess thiol at room temperature is described. The choice of silica gel, either pre-calcined or moistened with water, exhibited notable regioselectivity in the formation of dithioethers. Plausible mechanistic routes were explored and postulated.

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3

Moorhoff, Cornelis M., Wayne D. Cook, Fei Chen, et al. "Synthesis of Acyclic, Symmetrical 3,3'-Allyl Dithioethers, from the Alkylation of 3-Mercapto-2-mercaptomethylprop-1-ene in the Presence of Sodium Hydride." Australian Journal of Chemistry 64, no. 8 (2011): 1083. http://dx.doi.org/10.1071/ch11117.

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A novel method where 3,3′-allyl dithioethers have been prepared from 3-mercapto-2-mercaptomethylprop-1-ene and two mol equivalent of alkyl halide in the presence of two mol equivalent of sodium hydride has been developed. Using this method, bisepoxide, 2,2′-(2-methylenepropane-1,3-diyl)bis(sulfanediyl)bis(methylene)dioxirane (8) has been synthesized from epichlorohydrin, whereas potassium carbonate was unable to deliver this product. These 3,3′-allyl dithioethers can be utilized either as monomers, or with further chemical reactions transformed into more complex monomers, for photoplastic poly

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4

Yuan, Xiao, Xiaoju Tan, Na Ding, Yongchun Liu, Xiaoxiao Li, and Zhigang Zhao. "NIS-promoted intermolecular bis-sulfenylation of allenamides via a two-step radical process: synthesis of 1,3-dithioethers." Organic Chemistry Frontiers 7, no. 18 (2020): 2725–30. http://dx.doi.org/10.1039/d0qo00690d.

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5

Yu, Guodian, Yingcong Ou, Danyao Chen, Yuanting Huang, Yan Yan, and Qian Chen. "Air-Induced Disulfenylation of Alkenes: Facile Synthesis of Vicinal Dithioethers." Synlett 31, no. 01 (2019): 83–86. http://dx.doi.org/10.1055/s-0039-1691493.

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A novel disulfenylation of alkenes with thiophenols and their corresponding disulfides by using air as the oxidant has been achieved. This transformation provides a facile and practical protocol for the synthesis of vicinal dithioethers under mild conditions.

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6

Chernova, Nina P., Nurgul A. Pirmanova, Tolebi Dzhienalyev, and Andrei S. Potapov. "Simple Synthesis of Pyrazole-derived Dithioethers." Procedia Chemistry 15 (2015): 277–81. http://dx.doi.org/10.1016/j.proche.2015.10.044.

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7

Heinz, Benjamin, Moritz Balkenhohl, and Paul Knochel. "Thiolation of Pyridine-2-sulfonamides using Magnesium Thiolates." Synthesis 51, no. 23 (2019): 4452–62. http://dx.doi.org/10.1055/s-0039-1690199.

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The thiolation of pyridine-2-sulfonamides using magnesium thiolates is reported. The ortho-functionalizations of these sulfonamides using TMPMgCl·LiCl (TMP = 2,2,6,6-tetramethylpiperidyl) followed by electrophilic quenching produced a range of 3-functionalized pyridine-2-sulfonamides, which were subsequently converted into the corresponding thioethers. Finally, symmetric or asymmetric diorganodisulfides were employed as electrophiles in a one-pot ortho-functionalization–thiolation procedure, leading to pyridine 2,3-disubstituted dithioethers.

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8

Flores-Santos, Leticia, Erika Martin, Montserrat Diéguez, Anna M. Masdeu-Bultó, and Carmen Claver. "Novel chiral dithioethers derived from l-tartaric acid." Tetrahedron: Asymmetry 12, no. 21 (2001): 3029–34. http://dx.doi.org/10.1016/s0957-4166(01)00504-3.

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9

Serita, Masanori, Makiko Tamaoki, and Koichi Itoh. "Vibrational spectra of cyclic dithioethers and their dications. 1. Vibrational spectra and structures of 1,5-dithiacyclooctane and related cyclic dithioethers." Journal of Physical Chemistry 92, no. 7 (1988): 1747–51. http://dx.doi.org/10.1021/j100318a010.

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10

Moorhoff, Cornelis M., Wayne D. Cook, Tara Schiller, Carl Braybrook та San H. Thang. "Synthesis of Symmetrical, Substituted (alkane-α,ω-diyl)(bis[3,3′-allyl dithioethers]) Monomers for Photoplastic Polymer Networks". Australian Journal of Chemistry 65, № 8 (2012): 1165. http://dx.doi.org/10.1071/ch12278.

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Novel symmetrical (alkane-α,ω-diyl)(bis[3,3′-allyl dithioethers]) compounds and their ether analogues, have been synthesised from (alkane-α,ω-diyl)bis([2-{chloromethyl}allyl]sulfane) precursors, for use in crosslinked polymers which exhibit photoplastic behaviour. Facile synthesis and purification of these monomers was achieved if the alkane-α,ω-diyl moiety had at least one oxygen atom in this linker. The number of sulfur atoms in these monomers was varied from four to two to zero to produce monomers which can be used to evaluate their importance on the photoplasticity behaviour.

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Dissertationen zum Thema "Dithioethers"

1

Saha, Sankar. "Synthesis, characterization of transition metal-dithioether complexes and catalytic applications in organic reactions." Thesis, University of North Bengal, 2019. http://ir.nbu.ac.in/handle/123456789/3640.

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2

Broeker, Jeffrey Lee. "Theoretical and experimental studies on oxidation and interactions of mono- and dithioethers and their derivatives." Diss., The University of Arizona, 1988. http://hdl.handle.net/10150/184506.

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The potential energy surface of naphtho (1,8-b,c) -1,5-dithiocin and its mono-, di-, tri-, and tetraoxides was analyzed by dynamic ¹H NMR spectroscopy, AM1 semiempirical calculations, and x-ray crystallography. The lowest energy conformers of these compounds in the solid state, the gas state, and in solution, as well as the energy barriers for the interconversion between their conformers are reported. The electronic structure of naphtho (1,8-b,c) -1,5-dithiocin was analyzed by the AM1 semiempirical method. An experimental method was developed to verify these calculations. Comparison of the rel

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Buchteile zum Thema "Dithioethers"

1

Jennings, J. Gregory, and Gregory L. Powell. "Reactivity of Dithioethers Toward [Re2X8]2−." In Metal-Metal Bonds and Clusters in Chemistry and Catalysis. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2492-6_32.

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Konferenzberichte zum Thema "Dithioethers"

1

Potapov, Andrei, Nina Chernova, Tolebi Dzhienalyev, and Andrei Khlebnikov. "Synthesis of Pyrazole-Derived Dithioethers Using in situ Generation of Dithiolate-Ions." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a010.

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