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Volumn 7, Issue 1, 2005, Pages 39-42

A novel three-component one-pot synthesis of 1H-imidazol-4-yl-pyridines

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; AMINE; CYANIDE; IMIDAZOLE DERIVATIVE; PYRIDINE DERIVATIVE;

EID: 12344263141     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0480269     Document Type: Article
Times cited : (30)

References (22)
  • 11
    • 12344314543 scopus 로고
    • Schaumann, E., Ed.; Georg-Thieme: Stuttgart, New York
    • For an overview on the synthesis of imidazoles, see: Ebel, K. In Houben-Weyl: Methoden der Organischen Chemie, Heiarene III, 1H-Imidazole; Schaumann, E., Ed.; Georg-Thieme: Stuttgart, New York, 1994; pp 1-215. For recent imidazole syntheses, see: (a) Henkel, B. Tetrahedron Lett. 2004, 45, 2219. (b) Sezen, B.; Sames, D. J. Am. Chem. Soc. 2003, 125, 5274. (c) Tan, K. L.; Bergman, R. G.; Ellmann, J. A. J. Am. Chem. Soc. 2002, 124, 13964.
    • (1994) Houben-Weyl: Methoden der Organischen Chemie, Heiarene III, 1H-Imidazole , pp. 1-215
    • Ebel, K.1
  • 12
    • 1242340488 scopus 로고    scopus 로고
    • For an overview on the synthesis of imidazoles, see: Ebel, K. In Houben-Weyl: Methoden der Organischen Chemie, Heiarene III, 1H-Imidazole; Schaumann, E., Ed.; Georg-Thieme: Stuttgart, New York, 1994; pp 1-215. For recent imidazole syntheses, see: (a) Henkel, B. Tetrahedron Lett. 2004, 45, 2219. (b) Sezen, B.; Sames, D. J. Am. Chem. Soc. 2003, 125, 5274. (c) Tan, K. L.; Bergman, R. G.; Ellmann, J. A. J. Am. Chem. Soc. 2002, 124, 13964.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2219
    • Henkel, B.1
  • 13
    • 0037936773 scopus 로고    scopus 로고
    • For an overview on the synthesis of imidazoles, see: Ebel, K. In Houben-Weyl: Methoden der Organischen Chemie, Heiarene III, 1H-Imidazole; Schaumann, E., Ed.; Georg-Thieme: Stuttgart, New York, 1994; pp 1-215. For recent imidazole syntheses, see: (a) Henkel, B. Tetrahedron Lett. 2004, 45, 2219. (b) Sezen, B.; Sames, D. J. Am. Chem. Soc. 2003, 125, 5274. (c) Tan, K. L.; Bergman, R. G.; Ellmann, J. A. J. Am. Chem. Soc. 2002, 124, 13964.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 5274
    • Sezen, B.1    Sames, D.2
  • 14
    • 0037184456 scopus 로고    scopus 로고
    • For an overview on the synthesis of imidazoles, see: Ebel, K. In Houben-Weyl: Methoden der Organischen Chemie, Heiarene III, 1H-Imidazole; Schaumann, E., Ed.; Georg-Thieme: Stuttgart, New York, 1994; pp 1-215. For recent imidazole syntheses, see: (a) Henkel, B. Tetrahedron Lett. 2004, 45, 2219. (b) Sezen, B.; Sames, D. J. Am. Chem. Soc. 2003, 125, 5274. (c) Tan, K. L.; Bergman, R. G.; Ellmann, 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    Ellmann, J.A.3
  • 21
    • 12344318602 scopus 로고    scopus 로고
    • note
    • 3 as solvent to remove the polar impurities. The resulting semipure product is purified via preparatory HPLC after evaporation of the solvent.
  • 22
    • 12344330826 scopus 로고    scopus 로고
    • note
    • 3 solution in methanol and 50 μL of a 0.1 M (n = 5 μmol isocyanide solution in methanol are added. The plate is shaken overnight at room temperature. The solvent is removed under reduced pressure. To analyze plate by fast LC-MS the residue was dissolved in 1:1 methanol/ water to give a 1 mM solution.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.