Facile access to sodium arylsulfinates via nucleophilic C S bond cleavage of 2-(arylsulfonyl)pyrimidines
Author:
Funder
National Research Foundation of Korea
Ministry of Science, ICT and Future Planning
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference53 articles.
1. Recent representative reviews, see: (a) D. Kaiser, I. Klose, R. Oost, J. Neuhaus, N. Maulide, Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts, Chem. Rev. 119 (2019) 8701-8780
2. (b) S. Liang, K. Hofman, M. Friedrich, G. Manolikakes, Recent Advances in the Synthesis and Direct Application of Sulfinate Salts, Eur. J. Org. Chem. 2020 (2020) 4664-4676
3. (c) D. -Q. Dong, Q. -Q. Han, S.-H. Yang, J.-C. Song, N. Li, Z.-L. Wang, X.-M. Xu, Recent Progress in Sulfonylation via Radical Reaction with Sodium Sulfinates, SulfinicAcids, Sulfonyl Chlorides or Sulfonyl Hydrazides ChemistrySelect 5 (2020) 13103- 13134
4. (d) J. Aziz, A. Hamze, An update on the use of sulfinate derivatives as versatile coupling partners in organic chemistry, Org. Biomol. Chem. 18 (2020), 9136-9159
5. (e) O. M. Mulina, A. I. Ilovaisky, V. D. Parshin, A. O. Terent'ev, Oxidative Sulfonylation of Multiple Carbon-Carbon bonds with Sulfonyl Hydrazides, Sulfinic Acids and their Salts, Adv. Synth. Catal. 362 (2020) 4579-4654 (f) R. J. Reddy, A. H. Kumari, Synthesis and applications of sodium sulfinates (RSO2Na): a powerful building block for the synthesis of organosulfur compounds, RSC Adv. 11 (2021) 9130-9221
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