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Transition-metal-free synthesis of 3-sulfenylated chromones via KIO3-catalyzed radical C(sp2)-H sulfenylation.


ABSTRACT: The reactions between o-hydroxylphenyl-functionalized enaminones and sulfonyl hydrazines providing 3-sulfenylated chromones via domino chromone ring construction and C(sp2)-H bond sulfenylation have been achieved under transition-metal-free conditions by using KIO3 as the only catalyst.

SUBMITTER: Guo Y 

PROVIDER: S-EPMC5629394 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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Transition-metal-free synthesis of 3-sulfenylated chromones via KIO<sub>3</sub>-catalyzed radical C(sp<sup>2</sup>)-H sulfenylation.

Guo Yanhui Y   Zhong Shanshan S   Wei Li L   Wan Jie-Ping JP  

Beilstein journal of organic chemistry 20170927


The reactions between <i>o</i>-hydroxylphenyl-functionalized enaminones and sulfonyl hydrazines providing 3-sulfenylated chromones via domino chromone ring construction and C(sp<sup>2</sup>)-H bond sulfenylation have been achieved under transition-metal-free conditions by using KIO<sub>3</sub> as the only catalyst. ...[more]

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