Generation of ArS-substituted flavone derivatives using aryl thiols as sulfenylating agents

Wannian Zhao; Ping Xie; Zhaogang Bian; Aihua Zhou; Haibo Ge; Ben Niu; Yingcai Ding

doi:10.1039/c5ra10763f

Generation of ArS-substituted flavone derivatives using aryl thiols as sulfenylating agents

Wannian Zhao, Ping Xie, Zhaogang Bian, Aihua Zhou, Haibo Ge, Ben Niu, Yingcai Ding

Chemistry and Biochemistry

Research output: Contribution to journal › Article › peer-review

29 Scopus citations

Abstract

The regioselective and metal-free sulfenylation of flavones was achieved under aerobic conditions with ammonium iodide salt as an inducer instead of traditional iodine/oxidant combinations. This method enables the generation of various ArS-substituted flavone derivatives in good to excellent yields under environmentally friendly conditions, which significantly enriches current flavone chemistry.

Original language	English
Pages (from-to)	59861-59864
Number of pages	4
Journal	RSC Advances
Volume	5
Issue number	74
DOIs	https://doi.org/10.1039/c5ra10763f
State	Published - 2015

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10.1039/c5ra10763f

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title = "Generation of ArS-substituted flavone derivatives using aryl thiols as sulfenylating agents",

abstract = "The regioselective and metal-free sulfenylation of flavones was achieved under aerobic conditions with ammonium iodide salt as an inducer instead of traditional iodine/oxidant combinations. This method enables the generation of various ArS-substituted flavone derivatives in good to excellent yields under environmentally friendly conditions, which significantly enriches current flavone chemistry.",

author = "Wannian Zhao and Ping Xie and Zhaogang Bian and Aihua Zhou and Haibo Ge and Ben Niu and Yingcai Ding",

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T1 - Generation of ArS-substituted flavone derivatives using aryl thiols as sulfenylating agents

AU - Zhao, Wannian

AU - Xie, Ping

AU - Bian, Zhaogang

AU - Zhou, Aihua

AU - Ge, Haibo

AU - Niu, Ben

AU - Ding, Yingcai

PY - 2015

Y1 - 2015

N2 - The regioselective and metal-free sulfenylation of flavones was achieved under aerobic conditions with ammonium iodide salt as an inducer instead of traditional iodine/oxidant combinations. This method enables the generation of various ArS-substituted flavone derivatives in good to excellent yields under environmentally friendly conditions, which significantly enriches current flavone chemistry.

AB - The regioselective and metal-free sulfenylation of flavones was achieved under aerobic conditions with ammonium iodide salt as an inducer instead of traditional iodine/oxidant combinations. This method enables the generation of various ArS-substituted flavone derivatives in good to excellent yields under environmentally friendly conditions, which significantly enriches current flavone chemistry.

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U2 - 10.1039/c5ra10763f

DO - 10.1039/c5ra10763f

M3 - Article

AN - SCOPUS:84937151004

SN - 2046-2069

VL - 5

SP - 59861

EP - 59864

JO - RSC Advances

JF - RSC Advances

IS - 74

ER -

Generation of ArS-substituted flavone derivatives using aryl thiols as sulfenylating agents

Abstract

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