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Volumn 22, Issue 25, 2016, Pages 8694-8699

Eosin Y (EY) Photoredox-Catalyzed Sulfonylation of Alkenes: Scope and Mechanism

Author keywords

alkyl sulfinates; photocatalysis; reaction mechanisms; transient spectroscopy; vinyl sulfones

Indexed keywords

CATALYSIS; OLEFINS; PHOTOCATALYSIS; PHOTOOXIDATION; SALTS; SPECTROSCOPIC ANALYSIS;

EID: 84966560516     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201601000     Document Type: Article
Times cited : (132)

References (66)
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    • Reaction works also without NaOH, but the yields were slightly higher upon addition of NaOH. Lithium sulfinates were used, because they can be easily prepared by the presented method (see the Supporting Information). The reactivity of sodium and lithium sulfinates is similar according to literature. This is also confirmed by the nearly identical oxidation potentials (see the Supporting Information
    • Reaction works also without NaOH, but the yields were slightly higher upon addition of NaOH. Lithium sulfinates were used, because they can be easily prepared by the presented method (see the Supporting Information). The reactivity of sodium and lithium sulfinates is similar according to literature. This is also confirmed by the nearly identical oxidation potentials (see the Supporting Information).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.