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Volumn 357, Issue 2-3, 2015, Pages 355-360

Lewis acid-catalyzed electrophilic trifluoromethylthiolation of (Hetero)arenes

Author keywords

Electron rich olefins; Gold catalysts; Heteroarenes; Iron catalysts; Trifluoromethylthiolation

Indexed keywords


EID: 84922664674     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201400717     Document Type: Article
Times cited : (100)

References (83)
  • 12
    • 84891565619 scopus 로고    scopus 로고
    • Synthesis Reactivity, Applications, Wiley-VCH, Weinheim
    • f) P. Kirsch, Modern Fluoroorganic Chemistry. Synthesis Reactivity, Applications, Wiley-VCH, Weinheim, 2004, pp 203-251;
    • (2004) Modern Fluoroorganic Chemistry , pp. 203-251
    • Kirsch, P.1
  • 54
    • 84927686651 scopus 로고    scopus 로고
    • In this manuscript, the authors also described C-H to C-SCF3 conversions of arenes and heteroarenes (13 examples) but in the presence of a stoichiometric amount of CF3SO3H or Me3SiCl (80 °C)
    • In this manuscript, the authors also described C-H to C-SCF3 conversions of arenes and heteroarenes (13 examples) but in the presence of a stoichiometric amount of CF3SO3H or Me3SiCl (80 °C).
  • 78
    • 84922642836 scopus 로고    scopus 로고
    • No pre-scrambling of deuterium and H/D exchange of the product was observed based on GC-MS analyses of the recovered starting material
    • No pre-scrambling of deuterium and H/D exchange of the product was observed based on GC-MS analyses of the recovered starting material.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.