Sulfoxide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sulfoxide" in English language version.

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archive.org

Audrieth, Ludwig F.; Kleinberg, Jacob (1953). Non-aqueous solvents. New York: John Wiley & Sons. p. 222. LCCN 52-12057.

doi.org

Patai S, Rappoport Z, eds. (1995). Syntheses of Sulphones, Sulphoxides and Cyclic Sulphides. PATai's Chemistry of Functional Groups. John Wiley & Sons. doi:10.1002/9780470666357. ISBN 9780470666357.
Yanagisawa S, Itami K (2011). "Palladium/2,2′-bipyridyl/Ag₂CO₃ catalyst for C–H bond arylation of heteroarenes with haloarenes". Tetrahedron. 67 (24): 4425–4430. doi:10.1016/j.tet.2011.03.093.
Thomas R, Shoemaker CB, Eriks K (1966). "The Molecular and Crystal Structure of Dimethyl Sulfoxide, (H₃C)₂SO". Acta Crystallogr. 21: 12–20. doi:10.1107/S0365110X66002263..
Cunningham TP, Cooper DL, Gerratt J, Karadakov PB, Raimondi M (1997). "Chemical bonding in oxofluorides of hypercoordinate sulfur". Journal of the Chemical Society, Faraday Transactions. 93 (13): 2247–2254. doi:10.1039/A700708F.
Brecher J (2008). "Graphical representation standards for chemical structure diagrams" (PDF). Pure and Applied Chemistry. 80: 277–410 (on p. 389). doi:10.1351/pac200880020277. hdl:10092/2052. S2CID 98211634.
Fernández I, Khiar N (September 2003). "Recent developments in the synthesis and utilization of chiral sulfoxides". Chemical Reviews. 103 (9): 3651–705. doi:10.1021/cr990372u. PMID 12964880.
Roy KM (2002). "Sulfones and Sulfoxides". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a25_487. ISBN 978-3527306732.
Johnson CR, Keiser JE (1966). "Methyl Phenyl Sulfoxide". Org. Syntheses. 46: 78. doi:10.15227/orgsyn.046.0078.
Kagan HB, Chellappan SK, Lattanzi A (2015). "(R)-(+)-Phenyl methyl sulfoxide". E-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rn00456. ISBN 978-0471936237.
Holland, Herbert Leslie (1988). "Chiral Sulfoxidation by Biotransformation of Organic Sulfides". Chemical Reviews. 88 (3): 473–485. doi:10.1021/cr00085a002.
Peyronneau M, Roques N, Mazières S, Le Roux C (2003). "Catalytic Lewis Acid Activation of Thionyl Chloride: Application to the Synthesis of ArylSulfinyl Chlorides Catalyzed by Bismuth(III) Salts". Synlett (5): 0631–0634. doi:10.1055/s-2003-38358.
Bandgar BP, Makone SS (2004). "Lithium/Sodium Perchlorate Catalyzed Synthesis of Symmetrical Diaryl Sulfoxides". Synth. Commun. 34 (4): 743–750. doi:10.1081/SCC-120027723. S2CID 96348273.
Shiri L, Kazemi M (2017). "Deoxygenation of Sulfoxides". Res. Chem. Intermed. 43: 6007–6041. doi:10.1016/j.ccr.2014.09.008.
Sousa SC, Fernandes AC (2015). "Efficient deoxygenation methodologies catalyzed by oxo-molybdenum and oxo-rhenium complexes". Coord. Chem. Rev. 284: 67–92. doi:10.1007/s11164-017-2976-6. S2CID 102494853.
Michael Carrasco, Robert J. Jones, Scott Kamel, H. Rapoport, Thien Truong (1992). "N-(Benzyloxycarbonyl)-L-Vinylglycine Methyl Ester". Organic Syntheses. 70: 29. doi:10.15227/orgsyn.070.0029.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Cubbage, Jerry W.; Guo, Yushen; McCulla, Ryan D.; Jenks, William S. (1 December 2001). "Thermolysis of Alkyl Sulfoxides and Derivatives: A Comparison of Experiment and Theory". The Journal of Organic Chemistry. 66 (26): 8722–8736. doi:10.1021/jo0160625. PMID 11749600.
Koelewijn, P.; Berger, H. (2 September 2010). "Mechanism of the antioxidant action of dialkyl sulfoxides". Recueil des Travaux Chimiques des Pays-Bas. 91 (11): 1275–1286. doi:10.1002/recl.19720911102.
Kröhnke, C. (2016). "Polymer Stabilization". Reference Module in Materials Science and Materials Engineering. doi:10.1016/B978-0-12-803581-8.01487-9. ISBN 978-0-12-803581-8.
Armstrong, C.; Plant, M.A.; Scott, G. (February 1975). "Mechanisms of antioxidant action: the nature of the redox behaviour of thiodipropionate esters in polypropylene". European Polymer Journal. 11 (2): 161–167. doi:10.1016/0014-3057(75)90141-X.
Calligaris M (2004). "Structure and Bonding in Metal Sulfoxide Complexes: an Update". Coordination Chemistry Reviews. 248 (3–4): 351–375. doi:10.1016/j.ccr.2004.02.005.

handle.net

hdl.handle.net

Brecher J (2008). "Graphical representation standards for chemical structure diagrams" (PDF). Pure and Applied Chemistry. 80: 277–410 (on p. 389). doi:10.1351/pac200880020277. hdl:10092/2052. S2CID 98211634.

iupac.org

Brecher J (2008). "Graphical representation standards for chemical structure diagrams" (PDF). Pure and Applied Chemistry. 80: 277–410 (on p. 389). doi:10.1351/pac200880020277. hdl:10092/2052. S2CID 98211634.

loc.gov

lccn.loc.gov

Audrieth, Ludwig F.; Kleinberg, Jacob (1953). Non-aqueous solvents. New York: John Wiley & Sons. p. 222. LCCN 52-12057.

nih.gov

pubmed.ncbi.nlm.nih.gov

Fernández I, Khiar N (September 2003). "Recent developments in the synthesis and utilization of chiral sulfoxides". Chemical Reviews. 103 (9): 3651–705. doi:10.1021/cr990372u. PMID 12964880.
Cubbage, Jerry W.; Guo, Yushen; McCulla, Ryan D.; Jenks, William S. (1 December 2001). "Thermolysis of Alkyl Sulfoxides and Derivatives: A Comparison of Experiment and Theory". The Journal of Organic Chemistry. 66 (26): 8722–8736. doi:10.1021/jo0160625. PMID 11749600.

orgsyn.org

Iwai I, Ide J (1988). "2,3-Diphenyl-1,3-Butadiene". Organic Syntheses; Collected Volumes, vol. 6, p. 531.

semanticscholar.org

api.semanticscholar.org

Brecher J (2008). "Graphical representation standards for chemical structure diagrams" (PDF). Pure and Applied Chemistry. 80: 277–410 (on p. 389). doi:10.1351/pac200880020277. hdl:10092/2052. S2CID 98211634.
Bandgar BP, Makone SS (2004). "Lithium/Sodium Perchlorate Catalyzed Synthesis of Symmetrical Diaryl Sulfoxides". Synth. Commun. 34 (4): 743–750. doi:10.1081/SCC-120027723. S2CID 96348273.
Sousa SC, Fernandes AC (2015). "Efficient deoxygenation methodologies catalyzed by oxo-molybdenum and oxo-rhenium complexes". Coord. Chem. Rev. 284: 67–92. doi:10.1007/s11164-017-2976-6. S2CID 102494853.