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Difunctionalization of unactivated olefins selective electrochemical chlorosulfuration or chlorosulfoxidation
Direct difunctionalization of olefins-which are the most commonly used compounds in organic synthesis-is a powerful tool for rapid formation of structurally complex building blocks from readily available starting materials. However, difunctionalization of unactivated olefins remains a formidable cha...
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Published in: | Green chemistry : an international journal and green chemistry resource : GC 2022-08, Vol.24 (15), p.576-5763 |
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Main Authors: | , , , , |
Format: | Article |
Language: | |
Online Access: | Get full text |
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Summary: | Direct difunctionalization of olefins-which are the most commonly used compounds in organic synthesis-is a powerful tool for rapid formation of structurally complex building blocks from readily available starting materials. However, difunctionalization of unactivated olefins remains a formidable challenge. Herein, we describe a green, cost-effective, and eco-friendly electrochemical protocol for selective chlorosulfuration or chlorosulfoxidation of unactivated alkenes. This electrochemical method creates the potential possibility for the preparation of high-value-added products in a more sustainable and greener manner.
We introduced a combination of simple graphite electrodes, mild conditions, and a simple workup procedure for the selective preparation of sulfides or sulfoxides
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unactivated olefins and thiophenols through a green electrochemical protocol. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/d2gc02134j |