메뉴 건너뛰기




Volumn 11, Issue 9, 2013, Pages 1446-1450

A sterically demanding organo-superbase avoids decomposition of a naked trifluoromethyl carbanion directly generated from fluoroform

Author keywords

[No Author keywords available]

Indexed keywords

CHEMISTRY; POSITIVE IONS;

EID: 84875873164     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob27368g     Document Type: Article
Times cited : (104)

References (76)
  • 13
  • 29
    • 84875833860 scopus 로고    scopus 로고
    • e-EROS Encyclopedia of Reagents for Organic Synthesis
    • S. Rozen and A. Hagooly, e-EROS Encyclopedia of Reagents for Organic Synthesis, http://www3.interscience.wiley.com/cgi-bin/mrwhome/104554785/HOME, 2001
    • (2001)
    • Rozen, S.1    Hagooly, A.2
  • 74
    • 33846842713 scopus 로고    scopus 로고
    • ed., CRC, Boca Raton, FL, 91st edn, Successful examples of trifluoromethylation of disulfides with HCF3 using t-BuOK in THF were reported (ref. 10a). But this method cannot accept trifluoromethylation of carbonyl compounds (ref. 10a and see Scheme 3) During the reviewing process of our manuscript, a related trifluoromethylation of carbonyl compounds using HCF3 appeared. See
    • CRC Handbook of Chemistry and Physics, ed., W. H. Haynes, and, D. R. Lide, CRC, Boca Raton, FL, 91st edn, 2010-2011
    • (2010) CRC Handbook of Chemistry and Physics
    • Haynes, W.H.1    Lide, D.R.2
  • 76
    • 84875841046 scopus 로고    scopus 로고
    • C&EN, 12, DECEMBER 10
    • S. Ritter, C&EN, 12, DECEMBER 10, 2012
    • (2012)
    • Ritter, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.