Relevant bibliographies by topics / Selenosilanes

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Selenosilanes'

Author: Grafiati
Published: 10 March 2023

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Journal articles on the topic "Selenosilanes"

1

Degl'Innocenti, Alessandro, Antonella Capperucci, Giulio Castagnoli, Irene Malesci, Caterina Tiberi, and Brunella Innocenti. "Selenosilanes Mediated Stereoselective Synthesis of Polyfunctionalized Organic Molecules." Phosphorus, Sulfur, and Silicon and the Related Elements 183, no. 4 (April 1, 2008): 966–69. http://dx.doi.org/10.1080/10426500801900923.

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2

Tanini, Damiano, Tommaso Pecchi, Nikolai V. Ignat’ev, and Antonella Capperucci. "Ionic Liquids-Assisted Ring Opening of Three-Membered Heterocycles with Thio- and Seleno-Silanes." Catalysts 12, no. 10 (October 17, 2022): 1259. http://dx.doi.org/10.3390/catal12101259.

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Ring opening reactions of strained heterocycles (epoxides, aziridines, thiiranes) by silyl chalcogenides, such as thiosilanes and selenosilanes, can be efficiently performed in a variety of ionic liquids, which can behave as reaction media and in some cases also as catalysts. This protocol enables an alternative access to β-functionalized sulfides and selenides under mild conditions.
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3

Viglianisi, Caterina, Chiara Bonardi, Elena Ermini, Antonella Capperucci, Stefano Menichetti, and Damiano Tanini. "Selenosilane-Promoted Selective Mild Transformation of N-Thiophthalimides into Symmetric Disulfides." Synthesis 51, no. 08 (January 7, 2019): 1819–24. http://dx.doi.org/10.1055/s-0037-1610354.

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The reactivity of N-thiophthalimides with silyl chalcogenides is described. Treatment of N-thiophthalimides with bis(trimethylsilyl) sulfide [(Me3Si)2S] leads to the formation of a mixture of the corresponding disulfides and trisulfides. On the other hand, N-thiophthalimides react with bis(trimethylsilyl) selenide [(Me3Si)2Se] under TBAF catalysis to smoothly give variously substituted diaryl, divinyl, and dialkyl disulfides; formation of a selenotrisulfide (dithiaselane, RSSeSR) is rationalized as an intermediate. Exploiting the different chemical behavior of silyl chalcogenides, we have disclosed a novel, selective, and operationally simple method to access disulfides in good yields under mild conditions.
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4

Pandey, Ganesh, and Smita R. Gadre. "Generation and Mesolytic Dynamics of Organoselenane and Selenosilane Radical Ions: Development of Mechanistically Interesting and Synthetically Useful Chemistry†." Accounts of Chemical Research 37, no. 3 (March 2004): 201–10. http://dx.doi.org/10.1021/ar030037z.

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5

Kuciński, Krzysztof, Marcin Gruszczyński, and Grzegorz Hreczycho. "Ru‐catalyzed Formation of Thiosilanes and Selenosilanes using Dichalcogenides as a User‐Friendly Alternative to Thiols and Selenols." ChemCatChem, August 10, 2022. http://dx.doi.org/10.1002/cctc.202200961.

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6

Pandey, Ganesh, and Smita R. Gadre. "Generation and Mesolytic Dynamics of Organoselenane and Selenosilane Radical Ions: Development of Mechanistically Interesting and Synthetically Useful Chemistry." ChemInform 35, no. 24 (June 15, 2004). http://dx.doi.org/10.1002/chin.200424265.

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Dissertations / Theses on the topic "Selenosilanes"

1

Tanini, Damiano. "Stereoselective synthesis of functionalized open chain and heterocyclic sulfur and selenium containing compounds through the use of thiosilanes and organoselenosilanes." Doctoral thesis, 2016. http://hdl.handle.net/2158/1150967.

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In the course of this PhD thesis the research was mainly focused on the study of the reactivity of sulfurated and selenated derivatives with different substrates, aimed to develop mild and general approaches to obtain useful acyclic and cyclic compounds containing sulfur and/or selenium moieties, together with other heteroatoms (N, O). In this context, synthetic strategies based on the functionalization of bidentate compounds and on the reactivity of various silanes were studies. Particular attention was also paied to the determination of the antioxidant activity of selected, novel and simple molecules obtained during this work, as well as in the evaluation of their behaviour as synthetic mimics of glutathione peroxidase (GPx). In this connection was also studied the functionalization of natural substrates, such as eugenol, limonene, resveratrol and ascorbic acid, to introduce these chalchogens at selected positions of the natural molecular skeleton, in order to evaluate whether a synergistic effect could be obtained to increase their activity. During the period spent at the University of Bristol the research was focused on the chemistry of boronic esters as versatile intermediates in the asymmetric synthesis of a variety of organic compounds, with the aim to apply these findings also to the stereoselective synthesis of suitable enantioenriched precursors of more complex sulfurated and selenated derivatives.
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