Relevant bibliographies by topics / Swern oxidation

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

Academic literature on the topic 'Swern oxidation'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 June 2025

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Journal articles on the topic "Swern oxidation"

1

Guo, Tianfo, Yu Gao, Zhenjiang Li, Jingjing Liu, and Kai Guo. "Cyclopropenium-Activated DMSO for Swern-Type Oxidation." Synlett 30, no. 03 (2019): 329–32. http://dx.doi.org/10.1055/s-0037-1611183.

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Swern oxidation is widely used to convert alcohols into their corresponding carbonyl compounds. However, the conventional method with use of the volatile oxalyl chloride as an activator requires the reaction to be conducted below −60 °C. We discovered that 3,3-dichloro-1,2-diphenylcyclopropene (DDC) can be used as a new activator for Swern-type oxidations of alcohols, which can be conducted at −20 °C. This new protocol features mild and fast reactions with easy operation. Furthermore, the activator DDC is easy to handle, and diphenylcyclopropenone can be recovered quantitively. This new type o
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Bailey, Patrick D., Philip J. Cochrane, Frances Irvine, Keith M. Morgan, David P. J. Pearson, and Kenneth T. Veal. "Swern oxidation of tryptamine derivatives." Tetrahedron Letters 40, no. 24 (1999): 4593–96. http://dx.doi.org/10.1016/s0040-4039(99)00692-9.

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Richardson, Stewart K., and Robert J. Ife. "Swern oxidation of diaziridines to diazirines." Journal of the Chemical Society, Perkin Transactions 1, no. 6 (1989): 1172. http://dx.doi.org/10.1039/p19890001172.

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Bisai, Alakesh, M. Chandrasekhar, and Vinod K. Singh. "An alternative to the Swern oxidation." Tetrahedron Letters 43, no. 46 (2002): 8355–57. http://dx.doi.org/10.1016/s0040-4039(02)02004-x.

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Smith, Amos B., Tamara L. Leenay, Hsing-Jang Liu, Lloyd A.K.Nelson, and Richard G. Ball. "A Cavaet on the Swern Oxidation." Tetrahedron Letters 29, no. 1 (1988): 49–52. http://dx.doi.org/10.1016/0040-4039(88)80013-3.

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Gilbert, J. C., та Robert D. Selliah. "Swern oxidation of a hindered β-hydroxyester". Research on Chemical Intermediates 22, № 2 (1996): 91–101. http://dx.doi.org/10.1163/156856796x00548.

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Bailey, Patrick D., Philip J. Cochrane, Frances Irvine, Keith M. Morgan, David P. J. Pearson, and Kenneth T. Veal. "ChemInform Abstract: Swern Oxidation of Tryptamine Derivatives." ChemInform 30, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199933136.

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Al-Smadi, Derar, Thilak Enugala, Thomas Norberg, Jan Kihlberg, and Mikael Widersten. "Synthesis of Substrates for Aldolase-Catalysed Reactions: A Comparison of Methods for the Synthesis of Substituted Phenylacetaldehydes." Synlett 29, no. 09 (2018): 1187–90. http://dx.doi.org/10.1055/s-0036-1591963.

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Methods for the synthesis of phenylacetaldehydes (oxidation, one-carbon chain extension) were compared by using the synthesis of 4-methoxyphenylacetaldehyde as a model example. Oxidations of 4-methoxyphenylethanol with activated DMSO (Swern oxidation) or manganese dioxide gave unsatisfactory results; whereas oxidation with 2-iodoxybenzoic acid (IBX) produced 4-methoxyphenylacetaldehyde in reasonable (75%) yield. However, Wittig-type one-carbon chain extension with methoxymethylene-triphenylphosphine followed by hydro­lysis gave an excellent (81% overall) yield of 4-methoxyphenylacetaldehyde fr
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9

Dabbagh, Hossein A., and Ali Bagheri. "Thiomethoxymethylation of 5-Aryloxytetrazoles via Modified Swern Reagents." Journal of Chemical Research 2005, no. 3 (2005): 202–4. http://dx.doi.org/10.3184/0308234054213636.

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The modified Swern oxidation of 5-aryloxytetrazole (Ar- = 4-NO2-C6H4-, C6H5-, 2,6-dimethoxy-C6H3-) rings is described using combination of dimethyl sulfoxide with dicyclohexylcarbodiimide (DCC), oxalyl chloride or trifluoroacetic anhydride. The product observed at 1- and/or 2-position of tetrazole rings and yield depends on the substrate, electronic effect of aryloxy group and reaction conditions. It was possible to introduce a thiomethoxymethyl group at 1 and 2-position of tetrazole via rearrangement of Swern intermediate.
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Keirs, David, and Karl Overton. "Conversion of amines into imines by swern oxidation." Journal of the Chemical Society, Chemical Communications, no. 21 (1987): 1660. http://dx.doi.org/10.1039/c39870001660.

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Dissertations / Theses on the topic "Swern oxidation"

1

Vaccari, Thomas. "Synthesis of thioenol ether functionalized cyclooctyne and its orthogonal cycloaddition sequence." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2020. http://amslaurea.unibo.it/21705/.

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In this work, the synthesis of a new bifunctionalized cyclooctyne for a possible layer by layer surface functionalization is presented. The main objective is to find a more stable molecule than the literature known methyl enol ether substituted cyclooctyne. Accordingly, the two target functionalities are an internal alkyne group and a vinyl methyl sulfide group. The synthesis was achieved in 9 steps and consists first of all in the preparation of an aldehyde starting from 1,5-cyclooctadiene with a cyclopropanation reaction followed by a reduction and the SWERN oxidation to an aldehyde. The new
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Aquino, Estefania da Costa. "Síntese de 3-Trifluoracetil-1H-pirróis N-Aril Substituídos." Universidade Federal de Santa Maria, 2011. http://repositorio.ufsm.br/handle/1/10481.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico<br>This work presents a new, simple and versatile strategy for the synthesis of new N-aryl substituted 3-trifluoroacetyl-1H-pyrroles. The pyrroles were obtained by the reaction of 3-trifluoroacetyl-4,5-dihydrofuran with aryl amines of general formula ArNH2, and Ar= C6H4, 2-MeO(C6H4), 3-MeO(C6H4), 4-MeO(C6H4), 2-Me(C6H4), 3-Me(C6H4), 4-Me(C6H4), 3-F(C6H4), 4-F(C6H4), 3-Cl(C6H4), 4-Cl(C6H4), 4-OH(C6H4), 2-OH-5-Me(C6H3), 3-OH-4-Me(C6H3), 4-Br(C6H4) generating 1,1,1-trifluoro-3-(2-hydroxyethyl)-4-arylamino-3-beten-2-ones intermediates t
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Book chapters on the topic "Swern oxidation"

1

Li, Jie Jack. "Swern oxidation." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_295.

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Li, Jie Jack. "Swern oxidation." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_270.

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Li, Jie Jack. "Swern Oxidation." In Namensreaktionen. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-52850-7_148.

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Li, Jie Jack. "Swern oxidation." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_283.

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Li, Jie Jack. "Swern oxidation." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_251.

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Li, Jie Jack. "Swern Oxidation." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_148.

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Parrain, J. L., and J. Thibonnet. "Swern Oxidation." In Ketones. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00670.

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"90 Swern Oxidation." In Organic Chemistry: 100 Must-Know Mechanisms. De Gruyter, 2023. http://dx.doi.org/10.1515/9783110786835-090.

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Parrain, J. L., and J. Thibonnet. "By Swern Oxidation." In Ketones. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00694.

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"90. Swern Oxidation." In Organic Chemistry: 100 Must-Know Mechanisms. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110608373-090.

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