메뉴 건너뛰기




Volumn 47, Issue 36, 2008, Pages 6843-6846

Overall "pseudocationic" trifluoromethylation of dihydropyridines with triflic anhydride

Author keywords

Heterocycles; Lactones; Synthetic methods; Trifluoromethylation

Indexed keywords

HETEROCYCLES; LACTONES; SYNTHETIC METHODS; TRIFLUOROMETHYLATION;

EID: 52449125803     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200801879     Document Type: Article
Times cited : (27)

References (33)
  • 8
    • 53249126944 scopus 로고    scopus 로고
    • The shape of these signals is due to dynamic exchanging sites as a function of temperature. This will be discussed in a forthcoming paper.
    • The shape of these signals is due to dynamic exchanging sites as a function of temperature. This will be discussed in a forthcoming paper.
  • 10
    • 53249122507 scopus 로고    scopus 로고
    • Ed. R. Katritzky, University of Florida, Gainsville
    • R. Kumar, R. Chandra in Advances in heterocyclic Chemistry, Vol. 78 (Ed. R. Katritzky), University of Florida, Gainsville, 2001, pp. 259-313.
    • (2001) Advances in heterocyclic Chemistry , vol.78 , pp. 259-313
    • Kumar, R.1    Chandra, R.2
  • 13
    • 33847089440 scopus 로고
    • For general aspects on the chemistry of triflic anhydride, see for example: a
    • For general aspects on the chemistry of triflic anhydride, see for example: a) J. B. Hendrickson, D. D. Sternbach, K. W. Bair, Acc. Chem. Res. 1977, 10, 306-312;
    • (1977) Acc. Chem. Res , vol.10 , pp. 306-312
    • Hendrickson, J.B.1    Sternbach, D.D.2    Bair, K.W.3
  • 16
    • 34548255464 scopus 로고    scopus 로고
    • For a very recent discussion, see
    • For a very recent discussion, see: J. Yuasa, S. Yamada, S. Fukuzumi, Angew. Chem. 2007, 119, 3623-3625;
    • (2007) Angew. Chem , vol.119 , pp. 3623-3625
    • Yuasa, J.1    Yamada, S.2    Fukuzumi, S.3
  • 17
    • 34250807195 scopus 로고    scopus 로고
    • and references therein
    • Angew. Chem. Int. Ed. Engl. 2007, 46, 3553-3555, and references therein.
    • (2007) Angew. Chem. Int. Ed. Engl , vol.46 , pp. 3553-3555
  • 19
    • 53249096959 scopus 로고    scopus 로고
    • We are indebted to one of the referees for suggesting further experiments to assess the mechanism of the reaction and further uses of this approach
    • We are indebted to one of the referees for suggesting further experiments to assess the mechanism of the reaction and further uses of this approach.
  • 20
    • 0000731860 scopus 로고    scopus 로고
    • 3 species, see for example: a M. Tordeux, B. Langlois, C. Wakselman, J. Org. Chem. 1996, 61, 7545-7550;
    • 3 species, see for example: a) M. Tordeux, B. Langlois, C. Wakselman, J. Org. Chem. 1996, 61, 7545-7550;
  • 27
    • 33748661487 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 5432-5446;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 5432-5446
  • 29
    • 33846525992 scopus 로고    scopus 로고
    • and references therein;
    • Angew. Chem. Int. Ed. 2007, 46, 754-757, and references therein;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 754-757


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.