期刊
TETRAHEDRON LETTERS
卷 56, 期 27, 页码 4131-4134出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2015.05.050
关键词
Oxidation; Disulfides; Thiosulfonates; Organic synthesis; Oxone
资金
- Department of Science & Technology (DST), India through INSPIRE Faculty Fellowship [IFA12-CH-62]
A new method is described for the oxidation of aliphatic- and aromatic disulfides containing electron-donating and electron-withdrawing groups to their corresponding thiosulfonates using oxone in combination with the MX (MX = KBr, KCl, NaBr and NaCl). No obvious electronic effects influence the yields of thiosulfonates. Avoiding the usage of toxic and unstable reagents, mild reaction conditions, short reaction times and cost-effectiveness are advantages of this methodology when likened to known methods for thiosulfonates syntheses. (C) 2015 Elsevier Ltd. All rights reserved.
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