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Volumn 47, Issue 28, 2008, Pages 5215-5219

PdII-catalyzed monoselective ortho halogenation of C-H bonds assisted by counter cations: A complementary method to directed ortho lithiation

Author keywords

C H activation; Chemoselectivity; Counter cations; Ortho halogenation; Palladium

Indexed keywords

ACIDS; CHEMICAL REACTIONS; DIFFERENCE EQUATIONS; DIMETHYLFORMAMIDE; DOPING (ADDITIVES); MATHEMATICAL TRANSFORMATIONS; PALLADIUM; SALTS;

EID: 52949137408     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200705613     Document Type: Article
Times cited : (326)

References (68)
  • 1
    • 0141534438 scopus 로고    scopus 로고
    • For recent examples of total syntheses in which the insertion of a carbene or nitrene into a C-H bond was used as a strategic reaction, see: a A. Hinman, J. Du Bois, J. Am. Chem. Soc. 2003, 125, 11510;
    • For recent examples of total syntheses in which the insertion of a carbene or nitrene into a C-H bond was used as a strategic reaction, see: a) A. Hinman, J. Du Bois, J. Am. Chem. Soc. 2003, 125, 11510;
  • 4
    • 0037134813 scopus 로고    scopus 로고
    • For examples of total syntheses in which PdII, Pt II, or RhIIi-catalyzed C-H activation was used as a strategic reaction, see: a J. A. Johnson, N. Li, D. Sames, J. Am. Chem. Soc. 2002, 124, 6900;
    • IIi-catalyzed C-H activation was used as a strategic reaction, see: a) J. A. Johnson, N. Li, D. Sames, J. Am. Chem. Soc. 2002, 124, 6900;
  • 13
    • 0001108788 scopus 로고    scopus 로고
    • For reviews on C-H functionalization catalyzed by other metals, see: a
    • For reviews on C-H functionalization catalyzed by other metals, see: a) G. Dyker, Angew. Chem. 1999, 111, 1808;
    • (1999) Angew. Chem , vol.111 , pp. 1808
    • Dyker, G.1
  • 21
    • 53349112249 scopus 로고    scopus 로고
    • For Pd-catalyzed iodination reactions, see: a, US Patent 2003181759, 344284
    • For Pd-catalyzed iodination reactions, see: a) H. Kodama, T. Katsuhira, T. Nishida, T. Hino, K. Tsubata, US Patent 2003181759, 2003 [Chem. Abstr. 2001, 135, 344284];
    • (2001) Chem. Abstr , vol.135
    • Kodama, H.1    Katsuhira, T.2    Nishida, T.3    Hino, T.4    Tsubata, K.5
  • 27
    • 2342622185 scopus 로고
    • For stoichiometric Pd-mediated iodination reactions, see: a
    • For stoichiometric Pd-mediated iodination reactions, see: a) K. Carr, J. K. Sutherland, J. Chem. Soc. Chem. Commun. 1984, 1227;
    • (1984) J. Chem. Soc. Chem. Commun , pp. 1227
    • Carr, K.1    Sutherland, J.K.2
  • 35
    • 37049073681 scopus 로고    scopus 로고
    • IV complexes, see: a P. K. Byers, A. J. Canty, B. W. Skelton, A. H. White, J. Chem. Soc. Chem. Commun. 1986, 1722;
    • IV complexes, see: a) P. K. Byers, A. J. Canty, B. W. Skelton, A. H. White, J. Chem. Soc. Chem. Commun. 1986, 1722;
  • 62
    • 4544248275 scopus 로고    scopus 로고
    • 4NOAc, see: B. A. Steinhoff, I. A. Guzei, S. S. Stahl, J. Am. Chem. Soc. 2004, 126, 11268.
    • 4NOAc, see: B. A. Steinhoff, I. A. Guzei, S. S. Stahl, J. Am. Chem. Soc. 2004, 126, 11268.
  • 63
    • 0030598098 scopus 로고    scopus 로고
    • For the use of tetraalkyl ammonium salts in Heck-type reactions, see: a
    • For the use of tetraalkyl ammonium salts in Heck-type reactions, see: a) T. Jeffery, Tetrahedron 1996, 52, 10113;
    • (1996) Tetrahedron , vol.52 , pp. 10113
    • Jeffery, T.1
  • 65
    • 0037016413 scopus 로고    scopus 로고
    • For halide effects in transition-metal catalysis, see: a
    • For halide effects in transition-metal catalysis, see: a) K. Fagnou, M. Lautens, Angew. Chem. 2002, 114, 26;
    • (2002) Angew. Chem , vol.114 , pp. 26
    • Fagnou, K.1    Lautens, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.