Relevant bibliographies by topics / Deoxygenation of sulfoxides

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Deoxygenation of sulfoxides'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Deoxygenation of sulfoxides"

1

Ho, Tse-Lok, and C. WONG. "Deoxygenation of Sulfoxides." Synthesis 1973, no. 04 (2002): 206–7. http://dx.doi.org/10.1055/s-1973-22175.

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2

Shiri, Lotfi, and Mosstafa Kazemi. "Deoxygenation of sulfoxides." Research on Chemical Intermediates 43, no. 11 (2017): 6007–41. http://dx.doi.org/10.1007/s11164-017-2976-6.

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3

Mohanazadeh, Farajollah, Ahmad Reza Momeni, and Yousef Ranjbar. "Deoxygenation of sulfoxides with silica chloride." Tetrahedron Letters 35, no. 33 (1994): 6127–28. http://dx.doi.org/10.1016/0040-4039(94)88094-8.

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4

Kukushkin, Vadim Yu. "Metal-ion mediated deoxygenation of sulfoxides." Coordination Chemistry Reviews 139 (February 1995): 375–407. http://dx.doi.org/10.1016/0010-8545(94)01116-s.

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5

Suzuki, Kosuke, Jinu Jeong, Kazuya Yamaguchi, and Noritaka Mizuno. "Photoredox catalysis for oxygenation/deoxygenation between sulfides and sulfoxides by visible-light-responsive polyoxometalates." New Journal of Chemistry 40, no. 2 (2016): 1014–21. http://dx.doi.org/10.1039/c5nj01045d.

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6

García, Nuria, Manuel A. Fernández-Rodríguez, Patricia García-García, María R. Pedrosa, Francisco J. Arnáiz, and Roberto Sanz. "A practical and chemoselective Mo-catalysed sulfoxide reduction protocol using a 3-mercaptopropyl-functionalized silica gel (MPS)." RSC Advances 6, no. 32 (2016): 27083–86. http://dx.doi.org/10.1039/c6ra03106d.

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7

Sakai, Norio, Retsu Shimada, and Yohei Ogiwara. "Indium‐Catalyzed Deoxygenation of Sulfoxides with Hydrosilanes." Asian Journal of Organic Chemistry 10, no. 4 (2021): 845–50. http://dx.doi.org/10.1002/ajoc.202100063.

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8

Edinger, Carolin, and Siegfried R. Waldvogel. "Electrochemical Deoxygenation of Aromatic Amides and Sulfoxides." European Journal of Organic Chemistry 2014, no. 24 (2014): 5144–48. http://dx.doi.org/10.1002/ejoc.201402714.

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9

Porwal, Digvijay, and Martin Oestreich. "B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes." Synthesis 49, no. 20 (2017): 4698–702. http://dx.doi.org/10.1055/s-0036-1588476.

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B(C6F5)3 is shown to catalyze the deoxygenation of sulfoxides and sulfones to the corresponding sulfides with Et3SiH as the stoichiometric hydride source. While the method is limited in terms of functional group tolerance, it is applicable to the reduction of alkyl/aryl-, aryl/aryl-, and alkyl/alkyl-substituted sulfoxides, including the benzyl/benzyl-substituted derivative. The same protocol converts alkyl/aryl- but not aryl/aryl-substituted sulfones into sulfides.
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10

Nagasawa, Kazuo, Akemi Yoneta, Toshiyuki Umezawa, and Keiichi Ito. "Facile Deoxygenation of Sulfoxides by Using Metal/Chiloromethylsilanes." HETEROCYCLES 26, no. 10 (1987): 2607. http://dx.doi.org/10.3987/r-1987-10-2607.

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Dissertations / Theses on the topic "Deoxygenation of sulfoxides"

1

Nag, Mrinmoy. "Sulfoxides of thiophene and dibenzothiophene : a mechanistic study of photochemical deoxygenation /." 2005.

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Book chapters on the topic "Deoxygenation of sulfoxides"

1

Mapelli, Claudio, and Katerina Leftheris. "A rapid and efficient method of deoxygenation of sulfoxides applied to the reduction of methionine sulfoxide in peptide synthesis." In Peptides 1992. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1470-7_80.

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2

Drabowicz, J., P. Kiełbasiński, and M. Mikołajczyk. "Iodotrimethylsilane-Induced Elimination–Deoxygenation of Sulfoxides." In Ene-X Compounds (X=S, Se, Te, N, P). Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-033-00117.

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3

Drabowicz, J., P. Kiełbasiński, and M. Mikołajczyk. "Deoxygenation of Alk-1-enyl Sulfoxides." In Ene-X Compounds (X=S, Se, Te, N, P). Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-033-00118.

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4

Rehder, Dieter. "Oxo-transfer proteins based on molybdenum, tungsten, and vanadium." In Bioinorganic Chemistry. Oxford University Press, 2014. http://dx.doi.org/10.1093/hesc/9780199655199.003.0007.

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Abstract:
This chapter takes a closer look at early transition metals molybdenum, tungsten, and vanadium which are involved in many catalytically conducted two-electron transfer reactions, commonly accompanied by oxygenation and deoxygenation. Nature employs these metals as active centres in enzymes in a variety of oxidation and reduction reactions. These elements are also used in industrial contexts, commonly in steel production or, in the form of their oxides, to catalyze oxidation reactions, exploiting the ease of the change in oxidation states. The chapter discusses the Molybdo- and tungsto-pyranopt
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5

Taber, Douglass F. "Reduction of Organic Functional Groups." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0011.

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Cornelis J. Elsevier of the University of Amsterdam developed (ACS Catal. 2014, 4, 1349) an improved Pd-based protocol for the hydrogenation of an alkyne 1 to the Z-alkene 2. Yongbo Zhou and Shuang-Feng Yin of Hunan University showed (Adv. Synth. Catal. 2014, 356, 765) that under Cu catalysis, hypophosphorous acid selec­tively reduced the terminal alkyne of 3 to the ene-yne 4. Hidefumi Makabe of Shinshu University found (Tetrahedron Lett. 2014, 55, 2822) that the iodoalkyne 5 was reduced to the iodoalkene 6 by diimide, conveniently generated from the arenesulfo­nyl hydrazide. Manat Pohmakotr o
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Journal articles
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