메뉴 건너뛰기




Volumn , Issue 20, 2011, Pages 3209-3219

Transition-metal-catalyzed C-H functionalization for the synthesis of substituted pyridines

Author keywords

acylation; alkenyl ation; alkylation; arylation; C H functionalization; pyridine; transition metal catalysis

Indexed keywords

ARYLATIONS; C-H FUNCTIONALIZATION; CARBON-CARBON BOND; CARBON-CARBON BOND-FORMING REACTIONS; FUNCTIONALIZATIONS; SELECTIVE FUNCTIONALIZATION; TRANSITION METAL CATALYSTS; TRANSITION-METAL CATALYSIS;

EID: 80053899534     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260212     Document Type: Article
Times cited : (205)

References (55)
  • 10
    • 0012397313 scopus 로고
    • For a review, see
    • For a review, see:, Snieckus V, Chem. Rev. 1990 90 879
    • (1990) Chem. Rev. , vol.90 , pp. 879
    • Snieckus, V.1
  • 15
    • 0141677747 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see:, Varela J A., Saá C, Chem. Rev. 2003 103 3787
    • (2003) Chem. Rev. , vol.103 , pp. 3787
    • Varela, J.A.1    Saá, C.2
  • 16
    • 33744510833 scopus 로고    scopus 로고
    • For recent general reviews, see: Dyker G. Wiley-VCH Weinheim
    • For recent general reviews, see: Handbook of C-H Transformations Dyker G Wiley-VCH Weinheim 2005
    • (2005) Handbook of C-H Transformations
  • 24
    • 70350780276 scopus 로고    scopus 로고
    • For recent reviews, see
    • For recent reviews, see:, Bellina F, Rossi R, Tetrahedron 2009 65 10269
    • (2009) Tetrahedron , vol.65 , pp. 10269
    • Bellina, F.1    Rossi, R.2
  • 29
    • 33644502831 scopus 로고    scopus 로고
    • For related mechanistic studies with 3-methyl-3,4-dihydroquinazoline, see
    • For related mechanistic studies with 3-methyl-3,4-dihydroquinazoline, see:, Wiedemann S H., Lewis J C., Bergman R G., Ellman J A., J. Am. Chem. Soc. 2006 128 2452
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 2452
    • Wiedemann, S.H.1    Lewis, J.C.2    Bergman, R.G.3    Ellman, J.A.4
  • 32
    • 0037184456 scopus 로고    scopus 로고
    • For a similar observation in rhodium-catalyzed alkylation of azoles, see
    • For a similar observation in rhodium-catalyzed alkylation of azoles, see:, Tan K L., Bergman R G., Ellman J A., J. Am. Chem. Soc. 2002 124 13964
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13964
    • Tan, K.L.1    Bergman, R.G.2    Ellman, J.A.3
  • 43
    • 58449085051 scopus 로고    scopus 로고
    • Potassium tert -butoxide mediated arylation of pyridine is also suggested to proceed through a radical-based mechanism, see
    • Potassium tert -butoxide mediated arylation of pyridine is also suggested to proceed through a radical-based mechanism, see:, Yanagisawa S, Ueda K, Taniguchi T, Itami K, Org. Lett. 2008 10 4673
    • (2008) Org. Lett. , vol.10 , pp. 4673
    • Yanagisawa, S.1    Ueda, K.2    Taniguchi, T.3    Itami, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.