Relevant bibliographies by topics / Sulfoxides

Academic literature on the topic 'Sulfoxides'

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Published: 4 June 2021
Last updated: 1 August 2024

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Journal articles on the topic "Sulfoxides"

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Kimura, Tsutomu, Koto Sekiguchi, Akane Ando, and Aki Imafuji. "Fritsch–Buttenberg–Wiechell rearrangement of magnesium alkylidene carbenoids leading to the formation of alkynes." Beilstein Journal of Organic Chemistry 17 (May 28, 2021): 1352–59. http://dx.doi.org/10.3762/bjoc.17.94.

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A series of 1-heteroatom-substituted vinyl p-tolyl sulfoxides were prepared and treated with organometallic reagents to evaluate which combination of sulfoxides and organometallic reagents yielded alkynes the most efficiently. The use of 1-chlorovinyl p-tolyl sulfoxide and isopropylmagnesium chloride was optimal for this purpose. A variety of 1-chlorovinyl p-tolyl sulfoxides were prepared from carbonyl compounds and chloromethyl p-tolyl sulfoxide and were converted into alkynes via the sulfoxide/magnesium exchange reaction and subsequent Fritsch–Buttenberg–Wiechell (FBW) rearrangement of the resulting magnesium alkylidene carbenoids. The mechanism of the FBW rearrangement of magnesium alkylidene carbenoids was studied by using 13C-labeled sulfoxides and by using DFT calculations.
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Kou, K. G. M., and V. M. Dong. "Tandem rhodium catalysis: exploiting sulfoxides for asymmetric transition-metal catalysis." Organic & Biomolecular Chemistry 13, no. 21 (2015): 5844–47. http://dx.doi.org/10.1039/c5ob00083a.

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Sulfoxides are uncommon substrates for transition-metal catalysis due to their propensity to inhibit catalyst turnover. We have developed the first DKR of racemic allylic sulfoxides where rhodium catalyzed both sulfoxide epimerization and alkene hydrogenation.
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Salom-Roig, Xavier, and Claude Bauder. "Recent Applications in the Use of Sulfoxides as Chiral Auxiliaries for the Asymmetric Synthesis of Natural and Biologically Active Products." Synthesis 52, no. 07 (January 27, 2020): 964–78. http://dx.doi.org/10.1055/s-0039-1690803.

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The contribution of chiral sulfoxides as versatile auxiliaries in the field of organic chemistry has shown a prevalent interest in the asymmetric synthesis of natural products during the last 45 years. In this short review, we report the recent applications of these chiral auxiliaries to the synthesis of natural and biological active products highlighted from 2010 to 2019. We hope to allow the reader to have an overview of the potential of sulfoxide chemistry in the field of enantio­selective synthesis.1 Introduction2 Diastereoselective Additions to Ketones2.1 Reduction of β-Keto Sulfoxides2.2 Reduction of β-Keto Sulfoxides Followed by Bromohydrin Forma tion3 Synthesis of an α-Amino α′-Sulfinyl Ketone Followed by Diastere oselective Reduction of the β-Keto Sulfoxide4 Diastereoselective Addition of Carbanionic Chiral Sulfoxides4.1 Addition to an Aldehyde4.1.1 Aldol Reactions4.1.2 Reformatsky-Type Reactions4.2 Additions to Chiral Sulfinimines5 Diastereoselective Cyclization Reactions Directed by a Chiral Sulf oxide5.1 1,4-Radical Additions5.2 Intramolecular Conjugate Additions5.3 Nazarov Cyclizations5.4 Diels–Alder Reactions6 Atropodiastereoselective Synthesis7 Conclusion
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S. Kadam, Satwashila, Niranjan S. Mahajan, Pankaj A. Jadhav, and Shashikant C. Dhawale. "SULFOXIDES AND SULFONES: REVIEW." Indian Drugs 60, no. 02 (March 2, 2023): 7–14. http://dx.doi.org/10.53879/id.60.02.12267.

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It has been established that sulfoxide with sulfones have distinct pharmacological effects. Commodity compounds like sulfoxide and sulfones find widespread use in many chemical disciplines. This is why organic chemists find the synthesis of sulfoxide and sulfones so interesting. In the process of oxidation, sulphides can transform into sulfoxides or sulfones. Comprehensive oxidation to the sulfones is significantly simpler than mild oxidation to the sulfoxide, but both can be achieved by the use of highly selective technologies.
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Tomkiel, Aneta M., Dorota Czajkowska-Szczykowska, Ewa Olchowik-Grabarek, Lucie Rárová, Szymon Sękowski, and Jacek W. Morzycki. "A Study on the Chemistry and Biological Activity of 26-Sulfur Analogs of Diosgenin: Synthesis of 26-Thiodiosgenin S-Mono- and Dioxides, and Their Alkyl Derivatives." Molecules 28, no. 1 (December 26, 2022): 189. http://dx.doi.org/10.3390/molecules28010189.

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A chemoselective procedure for MCPBA oxidation of 26-thiodiosgenin to corresponding sulfoxides and sulfone was elaborated. An unusual equilibration of sulfoxides in solution was observed. Moreover, α-alkylation of sulfoxide and sulfone was investigated. Finally, the biological activity of obtained compounds was examined.
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Holland, Herbert L., Cynthia G. Rand, Peter Viski, and Frances M. Brown. "Microbial oxidation of benzyl sulfides and bibenzyl by Mortierella isabellina and Helminthosporium species." Canadian Journal of Chemistry 69, no. 12 (December 1, 1991): 1989–93. http://dx.doi.org/10.1139/v91-287.

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The biotransformation of 1,2-diphenylethane by the fungus Mortierella isabellina ATCC 42613, and that of a series of alkyl benzyl sulfides by the fungi M. isabellina and Helminthosporium species NRRL 4671 have been studied. Mortierella hydroxylates 1,2-diphenylethane in low yield, giving (S)-1,2-diphenylethanol with an enantiomeric purity of 33%. Bioconversions of deuterium-labelled and racemic 1,2-diphenylethanol by M. isabellina demonstrate that this organism performs reversible oxidation/reduction of the alcohol. Biotransformations of n-alkyl benzyl sulfides by H. species give predominantly the (S) enantiomer of sulfoxide, with no sulfone formation, but M. isabellina, although showing a general preference for the oxidation of alkyl benzyl sulfides to (R) sulfoxides, also generates sulfones from n-alkyl benzyl sulfides in a time-dependent manner that suggests a stereoselective removal of (R) sulfoxide. The latter microorganism can be used, however, for the production of (R)-benzyl methyl and benzyl isopropyl sulfoxides, and gives (S)-benzyl tert-butyl sulfoxide in low yield. Key words: biotransformation, enzymes, sulfoxides.
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Massa, Antonio, Laura Capozzolo, and Arrigo Scettri. "Sulfoxides in the allylation of aldehydes in the presence of silicon tetrachloride and allyltributylstannane." Open Chemistry 8, no. 6 (December 1, 2010): 1210–15. http://dx.doi.org/10.2478/s11532-010-0099-7.

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AbstractSiCl4 can be conveniently activated by catalytic amounts of dimethyl sulfoxide or other readily-available sulfoxides for the allylation of aromatic, hetero-aromatic and unsaturated aldehydes in the presence of allyltributyl stannane. Chiral aryl methyl sulfoxides have been used to develop asymmetric allylation methods, as well as probe the aldehyde substrate scope.
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Somogyi, László. "Elimination, ring-contraction, and fragmentation reactions of 1-thioflavanone 1-oxides." Canadian Journal of Chemistry 79, no. 7 (July 1, 2001): 1159–65. http://dx.doi.org/10.1139/v01-096.

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Epimeric thioflavanone sulfoxides (2b) were selectively transformed into thioflavone (1a), thioaurone (3a), and di(2-cinnamoylphenyl) disulfide (4). Disulfide 4 can be recyclized into thioaurones (3a–c) and thioflavanones (2a,5) with heterolysis of the S—S bond. The 3-p-anisylidene sulfoxide analog of 2b (6) transforms, with fragmentation, into 4'-methoxythioaurone 3b.Key words: chalcone, ring contraction, sulfoxides, thioaurones, thioflavonoids.
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Holland, Herbert L., and Benito Munoz. "Fungal biotransformation of 1,3-oxathiolanes." Canadian Journal of Chemistry 66, no. 9 (September 1, 1988): 2299–303. http://dx.doi.org/10.1139/v88-364.

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A series of 2,2-disubstituted 1,3-oxathiolanes has been incubated with fungi known to be capable of efficient asymmetric oxidation of sulfides to sulfoxides. In three cases (2-phenyl-1,3-oxathiolane, 2-methyl-2-phenyl-1,3-oxathiolane, and 2-tert-butyl-2-phenyl-1,3-oxathiolane), sulfoxidation occurred to give a single diastereomer of sulfoxide, whose relative stereochemistry has been assigned by 1H nuclear magnetic resonance analysis. The sulfoxides were obtained as racemates or had low enantiomeric enrichment. In some cases ketones, assumed to be formed by spontaneous hydrolysis of oxathiolane sulfoxides, were obtained, together with their reduction products, secondary alcohols.
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Hrudková, Hana, Pavel Čefelín, and Václav Janout. "Polymer sulfoxides based on poly(vinyl alcohol) as effective catalysts of nucleophilic substitution reactions." Collection of Czechoslovak Chemical Communications 52, no. 9 (1987): 2204–11. http://dx.doi.org/10.1135/cccc19872204.

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Using the addition of alcohols to ethyl vinyl sulfoxide, a number of 2-alkoxyethyl ethyl sulfoxides were prepared, containing the following alkyls: methyl, ethyl, isopropyl, benzyl, and cyclohexyl. With a 10 mole % excess of alcohol the extent of the reaction was 70-95%. By a polymeranalogous reaction with poly(vinyl alcohol) and poly(ethylene-co-vinyl alcohol), copolymers poly[1-hydroxyethylene (74 mole %)-co-1-(2-ethylsulfinylethoxy)ethylene (26 mole %)] and poly[ethylene (62 mole %)-co-1-hydroxyethylene (35 mole %)-co-1-(2-ethylsulfinylethoxy)ethylene (3 mole %)] were prepared; the reaction with polymer alcohols requires the use of excess ethyl vinyl sulfoxide. These polymer sulfoxides were tested as catalysts of nucleophilic substitution reactions, using reactions of 1-bromooctane with sodium phenoxide, sodium iodide and potassium thiocyanate. They are more effective catalysts than polymer sulfoxides based on crosslinked poly(styrene) under the conditions of a two-phase (S-L) and three-phase (L-S-L) catalysis.
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Dissertations / Theses on the topic "Sulfoxides"

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Davies, Clair. "Capillary Electrophoretic Separation of Sulfoxides." TopSCHOLAR®, 1998. http://digitalcommons.wku.edu/theses/338.

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Chiral sulfoxides are most widely used in asymmetric synthesis. Their application as chiral synthons has now become a well-established and reliable strategy, mainly due to availability and high asymmetric induction exerted by the chiral sulfinyl group. Very few articles have been published on the separation of chiral sulfoxides; most involve HPLC or GC. The first separation of optically active sulfoxides was described by Phillips and co-workers. To date no work has been reported using capillary electrophoresis for the separation of alkylaryl sulfoxides. A series of alkylaryl sulfoxides were synthesized. Conditions for their separation were investigated using a modified 125 mM Boric acid (pH 8.5)/ 75 mM SDS buffer solution (MEKC buffer). Synthetic procedures for the preparation of these sulfoxides will be presented as well as separation results. The separation is based on the differential partition of solutes between the micelle and the bulk solution.
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Kendall, Jackie D. "Synthesis and enantioselective transformations of sulfoxides." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311838.

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Grainger, Richard Sheridan. "Cycloaddition reactions of C2-symmetric vinyl sulfoxides." Thesis, University of Sheffield, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387754.

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Lee, Danny Ka Ming. "Unsaturated sulfinates and sulfoxides in organic synthesis." HKBU Institutional Repository, 1995. http://repository.hkbu.edu.hk/etd_ra/47.

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Rowen, Catherine Carmel, and n/a. "A New Approach Towards Bicyclo[4.2.0]octan-1-ols: Synthetic and Mechanistic Studies." Griffith University. School of Science, 2003. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20030602.131636.

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The reaction between the lithium enolate of cyclohexanone and phenyl vinyl sulfoxide resulted in the formation of the novel bicyclooctanol sulfoxides 215-217 and the monoalkylated sulfoxide 218. The effects of variation in reaction time, temperature and concentration were studied. Under optimal conditions (10 minutes, -10°C and 0.085 M) the ratio of the bicyclooctanol sulfoxides 215-217 (75% yield) to the monoalkylated sulfoxide 218 was 95:5. The bicyclooctanol sulfoxides 215-217 were characterised as the sulfone derivatives, bicyclooctanol sulfones 219 and 220. X-ray crystal structures were used to determine the relative stereochemistry of the bicyclooctanol sulfoxides 215-217 and the bicyclooctanol sulfones 219 and 220. Bicyclo[4.2.0]octano-1-ol formation was determined to occur via an ionic mechanism. Mechanistic studies were carried out using variations in reaction lighting and reaction solvent, conducting the reaction in the presence of a radical trap and quenching the reaction with a deuterium label. The role of the counterion was determined to be important in the formation of the bicyclooctanol sulfoxides 215-217. Sequestering lithium ions with HMPA and substituting lithium with potassium favoured alkylation. Substituting the lithium enolate of cyclohexanone with the dimethylaluminium enolate of cyclohexanone resulted in a different distribution of the bicyclooctanol sulfoxides 215-217 and the formation of bicyclooctanol sulfoxide 243. Transition states to account for these differences have been proposed. The stability of the bicyclooctanol sulfoxides under conditions of acid, base and heating was studied. Thermal ring opening of the bicyclooctanol sulfoxides 215 and 216 to the monoalkylated sulfoxides 218A and 218B respectively occurred with retention of the configuration at sulfur. The relative stereochemistry of the individual bicyclooctanol sulfoxides 215-217 was considered to account for the observed stability in each case. The reaction between the lithium enolate of cyclohexanone and (R)-(+)-p-tolyl vinyl sulfoxide 193 gave the bicyclooctanol tolyl sulfoxides 246, 251 and 252 and the monoalkylated tolyl sulfoxide 247. This showed that both bond rotation in the side chain of the intermediate and epimerisation at sulfur occurred in the bicyclo[4.2.0]octan-1-ol forming process. The presence of the sulfoxide functionality in phenyl vinyl sulfoxide was determined to be crucial to the formation of bicyclo[4.2.0]octan-1-ols. In the reaction with the lithium enolate of cyclohexanone, phenyl vinyl sulfide gave no reaction, phenyl vinyl sulfone gave the bicyclic disulfones 260-265, ethyl acrylate gave the diesters 266-268 and diphenylvinylphosphine oxide gave the phosphine oxide 269. The cyclobutanol 270 and the ketone 271 were the products resulting from the reaction between the reaction between the lithium enolate of acetophenone and phenyl vinyl sulfoxide. This demonstrated potential scope for the cyclisation process using both cyclic and acyclic ketones.
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Rowen, Catherine Carmel. "A New Approach Towards Bicyclo[4.2.0]octan-1-ols: Synthetic and Mechanistic Studies." Thesis, Griffith University, 2003. http://hdl.handle.net/10072/367745.

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The reaction between the lithium enolate of cyclohexanone and phenyl vinyl sulfoxide resulted in the formation of the novel bicyclooctanol sulfoxides 215-217 and the monoalkylated sulfoxide 218. The effects of variation in reaction time, temperature and concentration were studied. Under optimal conditions (10 minutes, -10°C and 0.085 M) the ratio of the bicyclooctanol sulfoxides 215-217 (75% yield) to the monoalkylated sulfoxide 218 was 95:5. The bicyclooctanol sulfoxides 215-217 were characterised as the sulfone derivatives, bicyclooctanol sulfones 219 and 220. X-ray crystal structures were used to determine the relative stereochemistry of the bicyclooctanol sulfoxides 215-217 and the bicyclooctanol sulfones 219 and 220. Bicyclo[4.2.0]octano-1-ol formation was determined to occur via an ionic mechanism. Mechanistic studies were carried out using variations in reaction lighting and reaction solvent, conducting the reaction in the presence of a radical trap and quenching the reaction with a deuterium label. The role of the counterion was determined to be important in the formation of the bicyclooctanol sulfoxides 215-217. Sequestering lithium ions with HMPA and substituting lithium with potassium favoured alkylation. Substituting the lithium enolate of cyclohexanone with the dimethylaluminium enolate of cyclohexanone resulted in a different distribution of the bicyclooctanol sulfoxides 215-217 and the formation of bicyclooctanol sulfoxide 243. Transition states to account for these differences have been proposed. The stability of the bicyclooctanol sulfoxides under conditions of acid, base and heating was studied. Thermal ring opening of the bicyclooctanol sulfoxides 215 and 216 to the monoalkylated sulfoxides 218A and 218B respectively occurred with retention of the configuration at sulfur. The relative stereochemistry of the individual bicyclooctanol sulfoxides 215-217 was considered to account for the observed stability in each case. The reaction between the lithium enolate of cyclohexanone and (R)-(+)-p-tolyl vinyl sulfoxide 193 gave the bicyclooctanol tolyl sulfoxides 246, 251 and 252 and the monoalkylated tolyl sulfoxide 247. This showed that both bond rotation in the side chain of the intermediate and epimerisation at sulfur occurred in the bicyclo[4.2.0]octan-1-ol forming process. The presence of the sulfoxide functionality in phenyl vinyl sulfoxide was determined to be crucial to the formation of bicyclo[4.2.0]octan-1-ols. In the reaction with the lithium enolate of cyclohexanone, phenyl vinyl sulfide gave no reaction, phenyl vinyl sulfone gave the bicyclic disulfones 260-265, ethyl acrylate gave the diesters 266-268 and diphenylvinylphosphine oxide gave the phosphine oxide 269. The cyclobutanol 270 and the ketone 271 were the products resulting from the reaction between the reaction between the lithium enolate of acetophenone and phenyl vinyl sulfoxide. This demonstrated potential scope for the cyclisation process using both cyclic and acyclic ketones.
Thesis (PhD Doctorate)
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Faculty of Science
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Heer, Jag Paul. "New methods of asymmetric oxidation." Thesis, University of Liverpool, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.484195.

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Chan, Eddy Tsz Tak. "Unsaturated sulfoxides in organic synthesis : a new furan synthesis and total synthesis of isoquinolone alkaloids." HKBU Institutional Repository, 1991. https://repository.hkbu.edu.hk/etd_ra/3.

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Banjavšciªc, Marko Peter. "Infrared multiple-photon dissociation of small organic sulfoxides." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0020/NQ41366.pdf.

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Motto, John M. "Ã,ß-unsaturated sulfoxides and sulfinic acid derivatives." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ58363.pdf.

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Books on the topic "Sulfoxides"

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Kelly, Cornelius J. Stereoselective synthesis using sulfoxides. Dublin: University College Dublin, 1997.

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Lütz, Stephan. Prozessentwicklung der elektroenzymatischen Sulfoxidation mit Chloroperoxidase. Jülich: Forschungszentrum Jülich, Zentralbibliothek, 2005.

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Kochanewycz, Michael James. Oxidation of sulfides to sulfoxides using N-Phosphinoyloxaziridines. Birmingham: University of Birmingham, 1994.

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Saul, Patai, Rappoport Zvi, and Stirling C. J. M, eds. The Chemistry of sulphones and sulphoxides. Chichester [Sussex]: Wiley, 1988.

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Office, General Accounting. Acid rain: Emissions trends and effects in the eastern United States : report to Congressional requesters. Washington, D.C. (P.O. Box 37050, Washington, D.C. 20013): The Office, 2000.

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Office, General Accounting. Acid rain: Delays and management changes in the federal research program : report to the Chairman, Subcommittee on Oversight and Investigations, Committee on Energy and Commerce, House of Representatives. Washington, D.C: GAO, 1987.

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Office, General Accounting. Acid rain: Emissions trends and effects in the Eastern United States. Washington, D.C. (P.O. Box 37050, Washington, D.C. 20013): The Office, 2000.

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Schmid, Alex Adolf. Zur Infrarot-Laserchemie der Sulfoxide. [s.l.]: [s.n.], 1998.

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Science & Life Consultants Association., ed. Dimethyl sulfoxide (DMSO): Index of new information with authors & subjects. Washington, D.C: Abbe, 1994.

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Mailloux, Jeremy. The Effects of DMSO (Dimethyl Sulfoxide) on MCF-7 breast carcinoma cells. Sudbury, Ont: Laurentian University, 1999.

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Book chapters on the topic "Sulfoxides"

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Choudary, Boyapati M., Chinta Venkat, V. Reddy, Billakanti V. Prakash, Mannepalli L. Kantam, B. Sreedhar, Kiumar Bahrami, et al. "Oxidation of Sulfides and Sulfoxides." In Regio- and Stereo- Controlled Oxidations and Reductions, 279–302. Chichester, UK: John Wiley & Sons, Ltd, 2007. http://dx.doi.org/10.1002/9780470090244.ch9.

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Zeng, Jing, Yan Liu, Wei Chen, Xiang Zhao, Lingkui Meng, and Qian Wan. "Glycosyl Sulfoxides in Glycosylation Reactions." In Sulfur Chemistry, 367–98. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-25598-5_11.

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Ruano, José L. García, and Belén Cid de la Plata. "Asymmetric [4+2] Cycloadditions Mediated by Sulfoxides." In Topics in Current Chemistry, 1–126. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48956-8_1.

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"Sulfoxides." In Lead Optimization for Medicinal Chemists, 104–5. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527645640.ch21.

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Sandler, Stanley R., and Wolf Karo. "SULFOXIDES." In Sourcebook of Advanced Organic Laboratory Preparations, 182–85. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-08-092553-0.50023-6.

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Johnson, Carl R., and Mark P. Westrick. "Sulfoxides." In Methods in Enzymology, 281–86. Elsevier, 1987. http://dx.doi.org/10.1016/0076-6879(87)43054-1.

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Anna and George Wypych. "Sulfoxides." In Databook of Solvents, 689–96. Elsevier, 2014. http://dx.doi.org/10.1016/b978-1-895198-66-9.50023-0.

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Anna and George Wypych. "Sulfoxides." In Databook of Green Solvents, 501–12. Elsevier, 2014. http://dx.doi.org/10.1016/b978-1-895198-82-9.50016-6.

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Wypych, Anna, and George Wypych. "Sulfoxides." In Databook of Solvents, 810–15. Elsevier, 2024. http://dx.doi.org/10.1016/b978-1-77467-044-6.50024-2.

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Wypych, Anna, and George Wypych. "Sulfoxides." In Databook of Green Solvents, 553–64. Elsevier, 2024. http://dx.doi.org/10.1016/b978-1-77467-034-7.50017-x.

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Conference papers on the topic "Sulfoxides"

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Porto, Caio M., and Nelson H. Morgon. "Quantum Tunneling and Reaction Rates in Selenoxides and Sulfoxides Elimination." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202062.

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Selenoxides and sulfoxides elimination reactions are important, not only to Organic Chemistry synthesis, but also to other areas, as Biochemistry. These reactions were studied, using direct dynamics calculations, at the canonical variational theory (CVT) and small curvature tunneling (SCT) level. The calculated rate constants for the selenoxide reaction were in good agreement with experimental data, 8.83 × 10-5 s -1 and 3.20 × 10-5 s -1 , respectively. The rate constants for the sulfoxide reaction are very small at 37°C, namely 2.43 × 10-9 , and there is also a significant tunneling correction, which shows quantum tunneling effects occur in both reactions, although with very different magnitudes. One of the most striking difference comes from the barrier height, which is almost 2000 cm-1 bigger for the sulfoxide elimination, and helps to explain the difference in reaction rates.
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Wu, Fei, Xirong Chen, and Brad R. Weiner. "Photodissociation studies of cyclic sulfoxides." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by John W. Hepburn. SPIE, 1995. http://dx.doi.org/10.1117/12.220839.

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Ferioli, Federico, Elisa Giambanelli, and Filippo D'Antuono. "Evaluation of cysteine sulfoxides and volatile compounds in local garlic (Allium sativum L.) and elephant garlic (Allium ampeloprasum L.) populations from northern and central Italy." In VII South-Eastern Europe Syposium on Vegetables & Potatoes. University of Maribor Press, 2017. http://dx.doi.org/10.18690/978-961-286-045-5.13.

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Rack, Jeffrey J., Maksim Y. Livshits, and Jisoo Shin. "Photonastic effects in ruthenium sulfoxide polymers." In SPIE Organic Photonics + Electronics, edited by Joy E. Haley, Jon A. Schuller, Manfred Eich, and Jean-Michel Nunzi. SPIE, 2016. http://dx.doi.org/10.1117/12.2237391.

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Yu, Dongmei, Chao Zhang, Peiwu Qin, and Peter V. Cornish. "Characterization of Dimethyl Sulfoxide Binding Sites on Globular Trimeric Adiponectin." In Biomedical Engineering. Calgary,AB,Canada: ACTAPRESS, 2013. http://dx.doi.org/10.2316/p.2013.791-011.

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Mizuno, Kazuko, Takashi Sumikama, Yoshinori Tarnai, and Masahiko Tani. "Origins of Heat Evolution in Mixing Water and Dimethyl Sulfoxide." In 2018 43rd International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz 2018). IEEE, 2018. http://dx.doi.org/10.1109/irmmw-thz.2018.8509894.

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Altan, Semih. "Dimethyl Sulfoxide Suppresses Corneal Neovascularization in Acid Burn of Rabbits." In 15th International Congress of Histochemistry and Cytochemistry. Istanbul: LookUs Scientific, 2017. http://dx.doi.org/10.5505/2017ichc.pp-247.

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Gabler, Tomasz, Monika Janik, Marcin Koba, Malwina Sosnowska, Marta Kutwin, Ewa Sawosz Chwalibóg, and Mateusz Śmietana. "Real-time cytotoxicity monitoring using microcavity in-line Mach-Zehnder interferometer." In Optical Fiber Sensors. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/ofs.2022.th4.16.

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The work reports a microcavity in-line Mach-Zehnder interferometer sensor for real-time, label-free monitoring of a non-cancer bone marrow stromal cell line HS-5 responses to two cytotoxic agents, namely dimethyl sulfoxide (DMSO) and hydrogen peroxide (H2O2).
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Hamon, Cyrille, Claire Goldmann, Marta de Frutos, Doru Constantin, and Eric Hill. "Shape control of silver nanorods by ascorbic acid and dimethyl sulfoxide." In Internet NanoGe Conference on Nanocrystals. València: Fundació Scito, 2021. http://dx.doi.org/10.29363/nanoge.incnc.2021.001.

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Sano, T., and H. Schmidt. "Dual wavelength optofluidic distributed feedback dye laser on a single PDMS chip." In CLEO: Applications and Technology. Washington, D.C.: Optica Publishing Group, 2023. http://dx.doi.org/10.1364/cleo_at.2023.jw2a.1.

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We demonstrate two liquid-core distributed feedback (DFB) lasers operating side-by-side simultaneously at two different wavelengths with sub-mW thresholds from Rhodamine 6G dissolved in ethylene glycol and 4-(Dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4H-pyran in dimethyl sulfoxide on a single polydimethylsiloxane device.
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Reports on the topic "Sulfoxides"

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Blank, D. A., S. W. North, and D. Stranges. Three-body dissociations: The photodissociation of dimethyl sulfoxide at 193 nm. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/603618.

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LeMay, J. D. ,. LLNL. Swelling behavior of halthane 73-18 polyurethane adhesive in dimethyl sulfoxide (DMSO). Office of Scientific and Technical Information (OSTI), June 1996. http://dx.doi.org/10.2172/664427.

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So, Joanne D. An Essential Protein Repair Enzyme: Investigation of the Molecular Recognition Mechanism of Methionine Sulfoxide Reductase A. Fort Belvoir, VA: Defense Technical Information Center, May 2008. http://dx.doi.org/10.21236/ada485775.

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Krawiec, S. Cloning and expression of the sulfoxide/sulfone/sulfonate/sulfate genes in Pseudomonads and Thiobacillae. Tenth quarterly report. Office of Scientific and Technical Information (OSTI), February 1992. http://dx.doi.org/10.2172/10134616.

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Krawiec, S. Cloning and expression of the sulfoxide/sulfone/sulfonate/sulfate genes in Pseudomonads and Thiobacillae. [Pseudomonas, Thiobacillus, Rhodococcus]. Office of Scientific and Technical Information (OSTI), February 1992. http://dx.doi.org/10.2172/5653703.

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Adigun, Risikat. Insight into the Reactivity of Metastasis Inhibitor, Imidazolium trans-[tetrachloro (dimethyl sulfoxide)(imidazole)ruthenate(III)], with Biologically-active Thiols. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.378.

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Krawiec, S. Molecular biological enhancement of coal desulfurization: Cloning and expression of the sulfoxide/sulfone/sulfonate/sulfate genes in Pseudomonads and Thiobacillae. Office of Scientific and Technical Information (OSTI), November 1991. http://dx.doi.org/10.2172/5587437.

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Krawiec, S. Molecular biological enhancement of coal desulfurization: Cloning and expression of the sulfoxide/sulfone/sulfonate/sulfate genes in Pseudomonads and Thiobacillae. Office of Scientific and Technical Information (OSTI), August 1991. http://dx.doi.org/10.2172/6224900.

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Krawiec, S. Molecular biological enhancement of coal desulfurization: Cloning and expression of the sulfoxide/sulfone/sulfonate/sulfate genes in Pseudomonads and Thiobacillae. Eleventh quarterly report. Office of Scientific and Technical Information (OSTI), August 1992. http://dx.doi.org/10.2172/10159410.

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Krawiec, S. Molecular biological enhancement of coal desulfurization: Cloning and expression of the sulfoxide/sulfone/sulfonate/sulfate genes in Pseudomonads and Thiobacillae. [Rhodococcus erythropolis, Thiobacillus acidophilus, Thiobacillus novellus]. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/5065996.

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