Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/99109
標題: One-pot synthesis of thioesters with sodium thiosulfate as a sulfur surrogate under transition metal-free conditions
作者: Liao, Yen-Sen
Liang, Chien-Fu
梁健夫
Project: Organic & biomolecular chemistry, Volume 16, Issue 11, Page(s) 1871-1881.
摘要: 
In this paper, we report an efficient synthetic method for thioester formation from sodium thiosulfate pentahydrate, organic halides, and aryl anhydrides. In the one-pot two-step reactions developed in this study, sodium thiosulfate was used as the sulfur surrogate for acylation with anhydrides, followed by substitution with organic halides through the in situ generation of thioaroylate. Furthermore, two important organic compounds could be successfully synthesized using our developed method. The advantages of the one-pot two-step reactions are operational simplicity, structurally diverse products with 42%-90% yields, use of relatively low toxic and odourless reagents, and easy applicability to large-scale operation.
URI: http://hdl.handle.net/11455/99109
DOI: 10.1039/c8ob00178b
Appears in Collections:化學系所

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