A Convenient Synthesis of Sulfones via Light Promoted Coupling of Sodium Sulfinates and Aryl Halides | Zendy

Chen Lei | Zendy; Liang Jie | Zendy; Chen Zhenyu | Zendy; Chen Jie | Zendy; Yan Ming | Zendy; Zhang Xuejing | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

A Convenient Synthesis of Sulfones via Light Promoted Coupling of Sodium Sulfinates and Aryl Halides

Author(s) -

Chen Lei,

Liang Jie,

Chen Zhenyu,

Chen Jie,

Yan Ming,

Zhang Xuejing

Publication year - 2019

Publication title -

advanced synthesis and catalysis

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.541

H-Index - 155

eISSN - 1615-4169

pISSN - 1615-4150

DOI - 10.1002/adsc.201801390

Subject(s) - chemistry , aryl , halide , photochemistry , catalysis , aryl radical , electron transfer , photocatalysis , photoredox catalysis , acceptor , combinatorial chemistry , organic chemistry , alkyl , physics , condensed matter physics

A convenient and ecient synthesis of sulfones from sulfinates and aryl halides was developed. The reaction occurred under UV irradiation without transition metal catalyst or photocatalyst. A radical pathway via single‐electron transfer (SET) of electron donor‐acceptor (EDA) complex was proposed based on UV‐vis spectroscopy, radical inhibiting and trapping experiments.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research