Three-Component Tandem Amidosulfenylation of Alkenes for the Synthesis of β-Succinimide Sulfides

Yao, Lin; Li, Wenjian; Xiao, Fuhong; Deng, Guo-Jun

doi:10.1021/acs.joc.3c01518

Search citation statements

Order By: Relevance

Paper Sections

Select...

Introduction1

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2024

Publication Types

Select...

Article3

Relationship

Self Cite0

Independent3

Authors

Journals

Cited by 3 publications

(1 citation statement)

References 62 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…In 2018, Prof. Lei described an electrochemical oxidative aminosulfenylation of alkenes ( Yuan et al, 2018 ). Very recently, Deng’s group disclosed that NIS could be used as both a radical initiator and an N-nucleophile, enabling a metal-free amidosulfenylation of alkenes with disulfides ( Yao et al, 2023 ). However, there are common problems associated with these methods.…”

Section: Introductionmentioning

confidence: 99%

Aminothiolation of alkenes with azoles and Bunte salts

Ouyang,

Chai,

et al. 2024

Front. Chem.

View full text Add to dashboard Cite

show abstract

Section: Introductionmentioning

confidence: 99%

Aminothiolation of alkenes with azoles and Bunte salts

Ouyang,

Chai,

et al. 2024

Front. Chem.

View full text Add to dashboard Cite

show abstract

Intermolecular Sulfenoamination of Alkenes with Free‐Thiols and NIS to Access β‐Succinimide Sulfides

Chen,

Wang,

et al. 2024

Chemistry An Asian Journal

View full text Add to dashboard Cite

A convenient and practical multicomponent strategy for the sulfenoamination of alkenes was realized, which using free‐thiols as the sulfur‐reagent, NIS both as radical initiator and an N‐nucleophile. This protocol excellent in terms of transition‐metal‐free, good functional group tolerance, easily available substrates and facile scale‐up. And provided a direct‐ and general way to synthesize various β‐succinimide sulfides with high regioselectivity.

show abstract