|
[1]
|
Dunbar, K.L., Scharf, D.H., et al. (2017) Enzymatic Carbon-Sulfur Bond Formation in Natural Product Biosynthesis. Chemical Reviews, 117, 5521-5577. [Google Scholar] [CrossRef] [PubMed]
|
|
[2]
|
Zheng, L.W., Yang, C., Xu, Z.Z., Gao, F. and Xia, W.J. (2015) Difunctionalization of Alkenes via the Visible-Light-Induced Trifluoro-methylarylation/1,4-Aryl Shift/Desulfonylation Cascade Reactions. The Journal of Organic Chemistry, 80, 5730-5736. [Google Scholar] [CrossRef] [PubMed]
|
|
[3]
|
Ilardi, E.A., Vitaku, E. and Njardarson, J.T. (2014) Data-Mining for Sulfur and Fluorine: An Evaluation of Pharmaceuticals to Reveal Opportunities for Drug Design and Discovery. Journal of Medicinal Chemistry, 57, 2832-2842. [Google Scholar] [CrossRef] [PubMed]
|
|
[4]
|
Elattar, K.M., Fekri, A., et al. (2017) Sulfones in Heterocyclic Syn-thesis: Advances in the Chemistry of Phenyl Sulfonylacetophenone. Research on Chemical Intermediates, 43, 4227-4264. [Google Scholar] [CrossRef]
|
|
[5]
|
Yang, H., Carter, R.G. and Zakharov, L.N. (2008) Enantioselective Total Synthesis of Lycopodine. Journal of the American Chemical Society, 130, 9238-9239. [Google Scholar] [CrossRef] [PubMed]
|
|
[6]
|
Barry, M.T. and Dennis, P.C. (1981) Chemoselective Oxidation of Sulfides to Sulfones with Potassium Hydrogen Persulfate. Tetrahedron Letters, 14, 1287-1290. 90298-9 [Google Scholar] [CrossRef]
|
|
[7]
|
Sreedhar, B. and Rawat, V. (2012) A Regioselective Catalyst- and Additive-Free Synthesis of β-Ketosulfones from Aryl Acetylenes and Sodium Arenesulfinates. Synlett, 23, 413-417. [Google Scholar] [CrossRef]
|
|
[8]
|
Lu, Q.Q., Zhang, J., Zhao, G.L., Qi, Y., Wang, H.M. and Lei, A.W. (2013) Dioxygen-Triggered Oxidative Radical Reaction: Direct Aerobic Difunctionalization of Ter-minal Alkynes toward β-Ketosulfones. Journal of the American Chemical Society, 135, 11481-11484. [Google Scholar] [CrossRef] [PubMed]
|
|
[9]
|
Singh, A.K., Chawla, R. and Yadav, L.D. (2014) Aerobic Oxysul-fonylation of Alkynes in Aqueous Media: Highly Selective Access to β-Ketosulfones. Tetrahedron Letters, 55, 2845-2848. [Google Scholar] [CrossRef]
|
|
[10]
|
Cui, P., Liu, Q., et al. (2019) One-Pot Synthesis of Chiral β-Hydroxysulfones from Alkynes via Aerobic Oxysulfonylation and Asymmetric Reduction in MeOH/H2O. Green Chemistry, 21, 634-639. [Google Scholar] [CrossRef]
|
|
[11]
|
Li, F.X., Su, J.L., et al. (2021) A Glucose Oxidase-Hemoglobin System for Efficient Oxysulfonylation of Alkenes/Alkynes in Water. Molecular Catalysis, 500, Article ID: 111336. [Google Scholar] [CrossRef]
|
|
[12]
|
Pampana, V.K., Charpe, V.P., et al. (2021) Oxy-Sulfonylation of Terminal Alkynes via C-S Coupling Enabled by Copper Photoredox Ca-talysis. Green Chemistry, 23, 3569-3574. [Google Scholar] [CrossRef]
|
|
[13]
|
Holmquist, C.R. and Roskamp, E.J. (1992) Tin(II) Chloride Catalyzed Addition of Diazosulfones, Diazo Phosphine Oxides, and Di-azophosphonates to Aldehydes. Tetrahedron Letters, 33, 1131-1134.
91877-X [Google Scholar] [CrossRef]
|
|
[14]
|
Samakkanad, N., Katrun, P., et al. (2012) IBX/I2-Mediated Reaction of Sodium Arenesulfinates with Alkenes: Facile Synthesis of β-Ketosulfones. Synthesis, 44, 1693-1699. [Google Scholar] [CrossRef]
|
|
[15]
|
Lai, C.B., Xi, C.J., Jiang, Y.F. and Hua, R.M. (2005) One-Pot Approach for the Regioselective Synthesis of β-Ketosulfones Based on Acid-Catalyzed Reaction of Sulfonyl Chlorides with Arylacetylenes and Water. Tetrahedron Letters, 46, 513-515. [Google Scholar] [CrossRef]
|
|
[16]
|
吕进强, 曾竟, 阿布都热西提•阿布力克木. 原位产生二氧化锰催化构建S-S键[J]. 有机化学, 2020, 40(8): 2483-2490.
|
|
[17]
|
Yavari, I. and Shaabanzadeh, S. (2020) Electrochemical Synthesis of β-Ketosulfones from Switchable Starting Materials. Organic Letters, 22, 464-467. [Google Scholar] [CrossRef] [PubMed]
|
|
[18]
|
Binoyargha, D., Bhisma, K.P., et al. (2022) Visi-ble-Light-Mediated Synthesis of β-Ketosulfones Using g-C3N4 as a Recyclable Photocatalyst under Sustainable Conditions. Green Chemistry, 24, 7122-7130. [Google Scholar] [CrossRef]
|