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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 27, 1997 - Issue 8
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Original Articles

Hypervalent Iodine in Synthesis XXI: A Facile Method for the Preparation of Thiosulfonic S-Esters by the Oxidation of Diaryl Disulfides or Thiophenols with Phenyliodine (III) bis(Trifluoroacetate)

Min Xia Department of Chemistry, Hangzhou University, Hangzhou, P. R. China
&
Zhen-Chu Chen Department of Chemistry, Hangzhou University, Hangzhou, P. R. China
Pages 1301-1308 | Received 13 Jun 1996, Published online: 22 Aug 2006

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Nasser Iranpoor, Habib Firouzabadi & Ali Reza Pourali. (2006) Dinitrogen Tetroxide Impregnated Charcoal (N2O4/Charcoal): Selective Oxidation of Thiols to Disulfides or Thiosulfonates. Phosphorus, Sulfur, and Silicon and the Related Elements 181:3, pages 473-479.
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B. P. Bandgar & S. S. Pandit. (2004) Direct synthesis of thiosulfonic S-esters from sulfonic acids using cyanuric chloride under mild conditionsdirect synthesis of thiosulfonic s-esters. Journal of Sulfur Chemistry 25:5, pages 347-350.
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Articles from other publishers (17)

Guofu Zhang, Zhimin Sang, WenLiang Wu, Qiankun Fan & Chengrong Ding. (2022) Rongalite Promoted Reductive Esterification of Sulfonyl Chlorides: An Efficient Preparation of Sulfinic Esters. ChemistrySelect 7:41.
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A. K. Pandey, A. Kumar & S. K. Srivastava. (2022) Blue Light-Induced Coupling of N-Hydroxy Sulfonamides: An Efficient and Green Approach to Symmetrical Thiosulfonates. Russian Journal of Organic Chemistry 58:6, pages 844-849.
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Julia Strehl & Gerhard Hilt. (2021) Synthesis of Symmetrical and Unsymmetrical Thiosulfonates from Disulfides through Electrochemically Induced Disulfide Bond Metathesis and Site‐Selective Oxidation. European Journal of Organic Chemistry 2022:1.
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P. Mampuys, C. R. McElroyJ. H. ClarkR. V. A. Orru & B. U. W. Maes. (2019) Thiosulfonates as Emerging Reactants: Synthesis and Applications. Advanced Synthesis & Catalysis 362:1, pages 3-64.
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Pranab K. Shyam, Soobin Son & Hye-Young Jang. (2017) Copper-Catalyzed Sulfonylation of Alkenes and Amines by Using Thiosulfonates as a Sulfonylating Agent. European Journal of Organic Chemistry 2017:34, pages 5025-5031.
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Arisson Tranquilino, Silvia R.C.P. Andrade, Ana Paula M. da Silva, Paulo H. Menezes & Roberta A. Oliveira. (2017) Non-expensive, open-flask and selective catalytic systems for the synthesis of sulfinate esters and thiosulfonates. Tetrahedron Letters 58:13, pages 1265-1268.
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Akira Yoshimura & Viktor V. Zhdankin. (2016) Advances in Synthetic Applications of Hypervalent Iodine Compounds. Chemical Reviews 116:5, pages 3328-3435.
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A. Lattanzi. 2014. Comprehensive Organic Synthesis II. Comprehensive Organic Synthesis II 837 879 .
Viktor V. Zhdankin. 2013. Hypervalent Iodine Chemistry. Hypervalent Iodine Chemistry 145 336 .
Satoshi Iwata, Masato Senoo, Takeshi Hata & Hirokazu Urabe. (2013) Synthesis of S -Aryl Arenethiosulfonates from N , N -Di(arenesulfonyl)hydrazines: Reduction of Sulfonyl Chlorides with an Organic Reagent . Heteroatom Chemistry 24:4, pages 336-344.
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O.A. Rakitin. 2005. Comprehensive Organic Functional Group Transformations II. Comprehensive Organic Functional Group Transformations II 659 707 .
Gerald F. Koser, Thierry Ollevier & Valerie Desyroy. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Gerald F. Koser, Thierry Ollevier & Valerie Desyroy. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Thomas Wirth. 2003. Hypervalent Iodine Chemistry. Hypervalent Iodine Chemistry 185 208 .
Gerald F. Koser. 2003. Hypervalent Iodine Chemistry. Hypervalent Iodine Chemistry 173 183 .
Viktor V. Zhdankin & Peter J. Stang. (2002) Recent Developments in the Chemistry of Polyvalent Iodine Compounds. Chemical Reviews 102:7, pages 2523-2584.
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M. XIA & Z.‐C. CHEN. (2010) ChemInform Abstract: Hypervalent Iodine in Synthesis. Part 21. A Facile Method for the Preparation of Thiosulfonic S‐Esters by the Oxidation of Diaryl Disulfides or Thiophenols with Phenyliodine(III) Bis(trifluoroacetate).. ChemInform 28:29.
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