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Volumn 62, Issue 6, 2006, Pages 1110-1115

A very concise synthesis of a potent N-(1,3-thiazol-2-yl)pyridin-2-amine KDR kinase inhibitor

Author keywords

Aminothiazole; Chloropyridine; KDR; Pd catalysis; Piperazine; Xantphos

Indexed keywords

ALDEHYDE; AMINOTHIADIAZOLE; N (1,3 THIAZOL 2 YL)PYRIDIN 2 AMINE; PIPERAZINE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG; VASCULOTROPIN INHIBITOR;

EID: 29744465320     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.10.081     Document Type: Article
Times cited : (20)

References (43)
  • 17
  • 22
    • 0001029926 scopus 로고
    • Xantphos=4,5-bis(diphenylphosphino)-9,9-dimethylxanthene. The reason for the success of Xantphos is not clear, but it may be related to its trans-chelation configuration to the Pd. See Ref. 9g. For other examples where the use of Xantphos provides the best results, see Ref. 9e-j. (a) M. Kranenburg, Y.E.M. van der Burgt, P.C.J. Kamer, and P.W.N.M. van Leeuwen Organometallics 14 1995 3081
    • (1995) Organometallics , vol.14 , pp. 3081
    • Kranenburg, M.1    Van Der Burgt, Y.E.M.2    Kamer, P.C.J.3    Van Leeuwen, P.W.N.M.4
  • 43
    • 29744450949 scopus 로고    scopus 로고
    • note
    • 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.