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Synthesis 2017; 49(19): 4469-4477
DOI: 10.1055/s-0036-1589051
DOI: 10.1055/s-0036-1589051
paper
An Efficient Organic Electrosynthesis of β-Hydroxysulfones
We thank the Ministry of Science and Technology of the Republic of China for financial support (MOST 105-2113-M-037-001). This study was supported partially by Kaohsiung Medical University ‘Aim for the Top Universities Grant’ No. KMU-TP105PR02.Weitere Informationen
Publikationsverlauf
Received: 07. April 2017
Accepted after revision: 19. Mai 2017
Publikationsdatum:
25. Juli 2017 (online)
![](https://www.thieme-connect.de/media/synthesis/201719/lookinside/thumbnails/ss-2017-h0231-op_10-1055_s-0036-1589051-1.jpg)
Abstract
An efficient organic electrosynthesis of tertiary β-hydroxysulfones from functionalized α-methylstyrenes with substituted sodium sulfinates has been established. The novel electrosynthetic method provided the desired products in excellent yields, and the key structure was confirmed by X-ray single-crystal diffraction analysis.
Supporting Information
- Supporting information for this article is available online at https://doi.org /10.1055/s-0036-1589051.
- Supporting Information
- CIF File
-
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For reviews on sulfone compounds, see:
For biological reduction, see:
For chemical reduction, see:
For iodide, see:
For bromide, see:
For chloride, see: