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Volumn 66, Issue 33, 2010, Pages 6606-6612

Tandem Horner-Wadsworth-Emmons/Heck procedures for the preparation of 3-alkenyl-oxindoles: The synthesis of Semaxanib and GW441756

Author keywords

GW441756; Heck; Horner Wadsworth Emmons; Oxindoles; Palladium catalysis; Phosphonates; Semaxanib; Tandem reactions

Indexed keywords

ALDEHYDE; ANILIDE; GW 441756; OXINDOLE; PALLADIUM; PALLADIUM ACETATE; PROTEIN TYROSINE KINASE A; SEMAXANIB; TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM; UNCLASSIFIED DRUG;

EID: 77955665642     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.03.018     Document Type: Article
Times cited : (38)

References (57)
  • 1
    • 0038392407 scopus 로고    scopus 로고
    • For recent reviews on the synthesis and properties of oxindoles see
    • For recent reviews on the synthesis and properties of oxindoles see: (a) C. Marti, and E.M. Carreira Eur. J. Org. Chem. 2003 2209
    • (2003) Eur. J. Org. Chem. , pp. 2209
    • Marti, C.1    Carreira, E.M.2
  • 10
    • 30844466215 scopus 로고    scopus 로고
    • For recent approaches to 3-alkenyl-aza-oxindoles see
    • For recent approaches to 3-alkenyl-aza-oxindoles see: (a) E.J. Andreassen, and J.M. Bakke J. Heterocycl. Chem. 43 2006 49
    • (2006) J. Heterocycl. Chem. , vol.43 , pp. 49
    • Andreassen, E.J.1    Bakke, J.M.2
  • 32
    • 0042379984 scopus 로고    scopus 로고
    • For recent reviews on Pd-catalysed approaches to indoles see
    • (a) For recent reviews on Pd-catalysed approaches to indoles see: (a) A.B. Dounay, and L.E. Overman Chem. Rev. 103 2003 2945
    • (2003) Chem. Rev. , vol.103 , pp. 2945
    • Dounay, A.B.1    Overman, L.E.2
  • 36
    • 33947093958 scopus 로고
    • For early applications of the Heck reaction to oxindole synthesis see
    • For early applications of the Heck reaction to oxindole synthesis see: (a) N.A. Cortese, C.B. Ziegler Jr., B.J. Hrnjez, and R.F. Heck J. Org. Chem. 43 1978 2952
    • (1978) J. Org. Chem. , vol.43 , pp. 2952
    • Cortese, N.A.1    Ziegler Jr., C.B.2    Hrnjez, B.J.3    Heck, R.F.4
  • 39
    • 0036532291 scopus 로고    scopus 로고
    • For cascade routes to oxindoles which incorporate the Heck reaction see Ref. 16 and
    • For cascade routes to oxindoles which incorporate the Heck reaction see Ref. 16 and R. Grigg, E.L. Millington, and M. Thornton-Pett Tetrahedron Lett. 43 2002 2605
    • (2002) Tetrahedron Lett. , vol.43 , pp. 2605
    • Grigg, R.1    Millington, E.L.2    Thornton-Pett, M.3
  • 43
    • 29844449086 scopus 로고    scopus 로고
    • For recent applications of the Heck reaction to oxindole synthesis using 2-haloanilides see
    • For recent applications of the Heck reaction to oxindole synthesis using 2-haloanilides see: (a) A. Madin, C.J. O'Donnell, T. Oh, D.W. Old, L.E. Overman, and M.J. Sharp J. Am. Chem. Soc. 127 2005 18054
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 18054
    • Madin, A.1    O'Donnell, C.J.2    Oh, T.3    Old, D.W.4    Overman, L.E.5    Sharp, M.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.