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Volumn 45, Issue 8, 2006, Pages 1279-1282

Straightforward one-pot synthesis of trifluoromethyl sulfonium salts

Author keywords

Electrophiles; Reaction mechanisms; Sulfonium salts; Trifluoromethyl substituents

Indexed keywords

CHEMICAL EQUATION; ELECTROPHILES; SULFONIUM SALTS; TRIFLUOROMETHYL SUBSTITUENTS;

EID: 33746214615     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200503776     Document Type: Article
Times cited : (81)

References (25)
  • 11
  • 18
    • 33746186960 scopus 로고    scopus 로고
    • note
    • Sodium or potassium trifluoromethanesulfinate could be interchangeably used without influence on the yield.
  • 21
    • 33746247779 scopus 로고    scopus 로고
    • note
    • It should be remembered that water is also formed in this process and may concurrently be protonated by trifluoromethanesulfonic acid and/or hydrolyze trifluoromethanesulfonic anhydride; moreover, although the initiation process is no longer rate determining, it may nevertheless continue to participate in the reaction.
  • 24
    • 33746247778 scopus 로고    scopus 로고
    • note
    • Studies are also ongoing to develop a better understanding of the mechanism of the reduction reaction.
  • 25
    • 33746186958 scopus 로고    scopus 로고
    • note
    • 13C NMR spectra.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.