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

34Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

Guo, Y., Zhong, S., Wei, L., & Wan, J. P. (2017). Transition-metal-free synthesis of 3-sulfenylated chromones via KIO3-catalyzed radical C(sp2)–H sulfenylation. Beilstein Journal of Organic Chemistry, 13, 2017–2022. https://doi.org/10.3762/bjoc.13.199

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free