Visible-light-promoted one-pot synthesis of (3-keto sulfones from aryldiazo tetrafluoroborate salts via aerobic multicomponent reaction

被引:0
作者
Luu, Truong Giang [1 ]
Kim, Hee-Kwon [1 ,2 ]
机构
[1] Jeonbuk Natl Univ, Med Sch & Hosp, Dept Nucl Med, Jeonju 54907, South Korea
[2] Jeonbuk Natl Univ, Jeonbuk Natl Univ Hosp, Res Inst Clin Med, Biomed Res Inst, Jeonju 54907, South Korea
基金
新加坡国家研究基金会;
关键词
(3-Keto sulfones; Aryl diazonium; Visible-light-induced-reaction; Multicomponent reaction; DABSO; BETA-KETO SULFONES; VINYL SULFONES; OXYSULFONYLATION; EFFICIENT; DIOXYGEN; ALKENES; DIFUNCTIONALIZATION; KETOSULFONES; ALKYLATION; ALKYNES;
D O I
10.1016/j.tet.2024.134303
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
(3-Keto sulfone is a useful structure in organic chemistry and pharmaceuticals. In the present study, we developed a highly efficient visible-light-promoted reaction to prepare (3-keto sulfones under mild conditions. Synthesis was achieved via one-pot multi-component reaction of aryldiazo tetrafluoroborate salts, alkenes, and DABSO in the presence of air (O2) with rhodamine B serving as the photocatalyst. A variety of (3-keto sulfones were obtained at high yields by this one-pot operation under aerobic atmosphere. This oxysulfonylation procedure has benefits such as mild reaction conditions, a wide tolerance of functional groups, and simplicity, making it a promising choice for preparing valuable (3-keto sulfones.
引用
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页数:8
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