An electrochemical method for direct sulfonylation of BODIPYs under green conditions

Chen, Zhuo; Li, Chen; Liu, Kui; Wen, Li-Rong; Li, Ming; Zhang, Lin-Bao

doi:10.1039/d3qo01616a

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2024

Publication Types

Select...

Article4

Preprint1

Relationship

Self Cite2

Independent3

Authors

Journals

Cited by 6 publications

References 66 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

Electrochemical Cascade Annulation for the Synthesis of 3‐Sulfanylquinoline Derivatives Under Mild Conditions

Li,

Guo,

Chen

et al. 2024

Chin. J. Chem.

Self Cite

View full text Add to dashboard Cite

Comprehensive SummaryAn efficient electrochemical approach has been developed for the construction of 3‐sulfanylquinoline derivatives by treating phenylethynylbenzoxazinanones with disulfides in an undivided cell. The protocol provided a convenient route to functionalized quinolines with good functional group tolerance. Moreover, it does not require any metal catalysts or additives, furnishing a series of biological quinolines in moderate to good yields.

show abstract

Electrochemical Cascade Annulation for the Synthesis of 3‐Sulfanylquinoline Derivatives Under Mild Conditions

Li,

Guo,

Chen

et al. 2024

Chin. J. Chem.

Self Cite

View full text Add to dashboard Cite

show abstract

Electrochemical C-H thiocyanation of BODIPYs: Two birds with one stone of KSCN

Liu,

et al. 2024

Green Synthesis and Catalysis

View full text Add to dashboard Cite

Electrochemically Driven α,β-Dehydrogenation of Flavanones, Azaflavanones, and Thioflavanones

Mou,

Guo,

et al. 2024

Org. Lett.

View full text Add to dashboard Cite

Dehydrogenation of flavanones represents an ideal strategy to synthesize various flavones but remains challenging because of the requirements for rigorous conditions. Herein, a straightforward and efficient route for the synthesis of flavones via electrocatalysis is disclosed. This electro-oxidative approach shows a broad substrate scope, including azaflavanones and thioflavanones, which could be performed in an undivided cell without the removal of air or water and in the absence of metal catalysts, ligands, or external oxidants. Moreover, the combination of cyclic voltammetry, square wave voltammetry experiments, and density functional theory (DFT) calculations revealed the plausible mechanism.

show abstract

An electrochemical method for direct sulfonylation of BODIPYs under green conditions

Abstract: An environmentally benign electrochemical approach has been developed for the construction of β-sulfonylated BODIPYs by using sulfonylhydrazide as the sulfonyl source.

Cited by 6 publications

References 66 publications

Electrochemical Cascade Annulation for the Synthesis of 3‐Sulfanylquinoline Derivatives Under Mild Conditions

Electrochemical Cascade Annulation for the Synthesis of 3‐Sulfanylquinoline Derivatives Under Mild Conditions

Electrochemical C-H thiocyanation of BODIPYs: Two birds with one stone of KSCN

Electrochemically Driven α,β-Dehydrogenation of Flavanones, Azaflavanones, and Thioflavanones

Contact Info

Product

Resources

About