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Volumn , Issue 24, 2009, Pages 3636-3638

Efficient three-component one-pot synthesis of fully substituted pyridin-2(1H)-ones via tandem Knoevenagel condensation-ring-opening of cyclopropane-intramolecular cyclization

Author keywords

[No Author keywords available]

Indexed keywords

1 ACETYL 1 CARBAMOYL CYCLOPROPANE DERIVATIVE; AMINE; CYCLOPROPANE; MALONONITRILE; MORPHOLINE; PIPERIDINE; PROLINE DERIVATIVE; PYRIDIN 2(1H) ONE DERIVATIVE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67650639090     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b905742k     Document Type: Article
Times cited : (25)

References (30)
  • 12
    • 0000248247 scopus 로고
    • G. Jones ed., R. Adams, Organic Reactions, John Wiley and Sons, New York
    • The Knoevenagel condensation is one of the most useful carbon-carbon bond forming reactions in organic syntheses. See: G. Jones, in The Knoevenagel Condensation, ed., R. Adams, Organic Reactions, John Wiley and Sons, New York, 1967, vol. 15, pp. 204-599
    • (1967) The Knoevenagel Condensation , vol.15 , pp. 204-599
  • 14
    • 0014591875 scopus 로고
    • Pyridin-2(1H)-ones represent an important class of organic heterocycles with diverse pharmacological and biological activities. See: -624
    • F. Freeman Chem. Rev. 1969 69 591 624
    • (1969) Chem. Rev. , vol.69 , pp. 591
    • Freeman, F.1
  • 21
    • 84890597202 scopus 로고    scopus 로고
    • J. Zhu and H. Bienaymé, Wiley-VCH, Weinheim
    • Multicomponent Reactions, ed., J. Zhu, and, H. Bienaymé, Wiley-VCH, Weinheim, 2005
    • (2005) Multicomponent Reactions, Ed.
  • 27
    • 27144499189 scopus 로고    scopus 로고
    • The formation of 4 consists Knoevenagel condensation and subsequent intramolecular cyclization. For similar spiroannulated structures, see: -4568
    • A. M. Bernard A. Frongia P. P. Piras F. Secci M. Spiga Org. Lett. 2005 7 4565 4568
    • (2005) Org. Lett. , vol.7 , pp. 4565
    • Bernard, A.M.1    Frongia, A.2    Piras, P.P.3    Secci, F.4    Spiga, M.5
  • 28
    • 0141539238 scopus 로고    scopus 로고
    • Recently, some organocatalytic vinylogous Mannich reactions based on vinyl malononitriles have been developed. -4036
    • P. Langer G. Bose Angew. Chem., Int. Ed. 2003 42 4033 4036
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4033
    • Langer, P.1    Bose, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.