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Volumn 356, Issue 5, 2014, Pages 1079-1084

A general synthesis of α-trifluoromethylstyrenes through palladium-catalyzed cross-couplings with 1,1,1-trifluoroacetone tosylhydrazone

Author keywords

cross coupling; diazo compounds; palladium; tosylhydrazones; trifluoromethyl substituents

Indexed keywords


EID: 84897025963     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201300994     Document Type: Article
Times cited : (37)

References (105)
  • 18
    • 79958141712 scopus 로고    scopus 로고
    • O. A. Tomashenko, V. V. Grushin, Chem. Rev. 2011, 111, 4475. For some selected recent examples of aromatic trifluoromethylation, see
    • (2011) Chem. Rev. , vol.111 , pp. 4475
    • Tomashenko, O.A.1    Grushin, V.V.2
  • 56
    • 84870712049 scopus 로고    scopus 로고
    • trifluoromethylations with fluoroform of C, Si, S, and B centers
    • trifluoromethylations with fluoroform of C, Si, S, and B centers:, G. K. S. Prakash, P. V. Jog, P. T. D. Batamack, G. A. Olah, Science 2012, 338, 1324.
    • (2012) Science , vol.338 , pp. 1324
    • Prakash, G.K.S.1    Jog, P.V.2    Batamack, P.T.D.3    Olah, G.A.4
  • 103
    • 84882242969 scopus 로고    scopus 로고
    • The reaction of 1,1,1-trifluoroacetophenone tosylhydrazones with organolithium compounds has been recently reported and gives rise to terminal 1,1-difluorostyrenes
    • The reaction of 1,1,1-trifluoroacetophenone tosylhydrazones with organolithium compounds has been recently reported and gives rise to terminal 1,1-difluorostyrenes:, M. Kang, S.-A. Lee, N. Kang, B. Moon, Bull. Korean Chem. Soc. 2011, 32, 3022.
    • (2011) Bull. Korean Chem. Soc. , vol.32 , pp. 3022
    • Kang, M.1    Lee, S.-A.2    Kang, N.3    Moon, B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.