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Volumn 35, Issue 2, 2005, Pages 213-222

A simple and efficient method for selective single aldol condensation between arylaldehydes and acetone

Author keywords

Acetone; Aldol condensation; Aqueous sodium hydroxide; Arylaldehydes; Chalcones; Selectivity

Indexed keywords

ACETONE; ALDEHYDE DERIVATIVE; BENZALDEHYDE DERIVATIVE; CHALCONE DERIVATIVE; SODIUM HYDROXIDE;

EID: 14544291490     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-200048425     Document Type: Article
Times cited : (33)

References (18)
  • 2
    • 37049048398 scopus 로고
    • Chalcones and related compounds. Part IV. Addition of hydrogen cyanide to chalcones
    • Davey, W.; Tivey, D. J. Chalcones and related compounds. Part IV. Addition of hydrogen cyanide to chalcones. J. Chem. Soc. 1958, 1230-1236.
    • (1958) J. Chem. Soc. , pp. 1230-1236
    • Davey, W.1    Tivey, D.J.2
  • 3
    • 0002087663 scopus 로고
    • Benzalacetophenone
    • Clark, H. T., Leavitt, R. P., Eds.; John Wiley & Sons, Inc.: New York
    • Kohler, E. P.; Chadwell, H. M. Benzalacetophenone. In Org. Synth., 2nd Ed.; Clark, H. T., Leavitt, R. P., Eds.; John Wiley & Sons, Inc.: New York, 1941; Vol. Coll I, pp. 78-80.
    • (1941) Org. Synth., 2nd Ed. , vol.COLL I , pp. 78-80
    • Kohler, E.P.1    Chadwell, H.M.2
  • 4
    • 84993884851 scopus 로고
    • An improved procedure for the preparation of chalcones and related enones
    • Wattanasin, S.; Murphy, W. S. An improved procedure for the preparation of chalcones and related enones. Synthesis 1980, 647-650.
    • (1980) Synthesis , pp. 647-650
    • Wattanasin, S.1    Murphy, W.S.2
  • 5
    • 0030913328 scopus 로고    scopus 로고
    • 3-catalyzed aqueous aldol reactions of silyl enol ethers with aldehydes in the presence of a surfactant
    • 3-catalyzed aqueous aldol reactions of silyl enol ethers with aldehydes in the presence of a surfactant. Tetrahedron Lett. 1997, 38, 4559-4562.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4559-4562
    • Kobayashi, S.1    Wakabayashi, T.2    Nagayama, S.3    Oyamada, H.4
  • 6
    • 0000677232 scopus 로고
    • Organic reactions in aqueous media- with a focus on carbon-carbon bond formation
    • Li, C. J. Organic reactions in aqueous media- with a focus on carbon-carbon bond formation. Chem. Rev. 1993, 93, 2023-2035.
    • (1993) Chem. Rev. , vol.93 , pp. 2023-2035
    • Li, C.J.1
  • 7
  • 8
    • 0030989645 scopus 로고    scopus 로고
    • Aldol addition of aldehydes - A stereoselective approach to Syn-3-hydroxyaldehydes
    • Mahrwald, R.; Constisella, B.; Gundogan, B. Aldol addition of aldehydes - a stereoselective approach to Syn-3-hydroxyaldehydes. Tetrahedron Lett. 1997, 38, 4543-4544.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4543-4544
    • Mahrwald, R.1    Constisella, B.2    Gundogan, B.3
  • 10
    • 0001687008 scopus 로고    scopus 로고
    • Condensed heterocycles. Part I. Synthesis of pyrazolo, isoxazolo, pyrimido, pyranopyridinones and a novel bridgehead nitrogen heterocycles
    • Rao, K. A.; Gadre, J. N.; Pednekar, S. Condensed heterocycles. Part I. Synthesis of pyrazolo, isoxazolo, pyrimido, pyranopyridinones and a novel bridgehead nitrogen heterocycles. Indian J. Chem. 1997, 36B, 410-413.
    • (1997) Indian J. Chem. , vol.36 B , pp. 410-413
    • Rao, K.A.1    Gadre, J.N.2    Pednekar, S.3
  • 12
    • 0344861837 scopus 로고    scopus 로고
    • A highly active and reusable heterogeneous catalyst for the suzuki reaction: Synthesis of biaryls and polyaryls
    • Paul, S.; Clark, J. H. A highly active and reusable heterogeneous catalyst for the suzuki reaction: synthesis of biaryls and polyaryls. Green Chem. 2003, 5, 635-638.
    • (2003) Green Chem. , vol.5 , pp. 635-638
    • Paul, S.1    Clark, J.H.2
  • 13
    • 0347950980 scopus 로고    scopus 로고
    • Zinc mediated Friedel-Crafts acylation in solvent-free conditions under microwave irradiation
    • and references cited therein
    • Paul, S.; Nanda, P.; Gupta, R.; Loupy, A. Zinc mediated Friedel-Crafts acylation in solvent-free conditions under microwave irradiation. Synthesis 2003, 2877-2881 and references cited therein.
    • (2003) Synthesis , pp. 2877-2881
    • Paul, S.1    Nanda, P.2    Gupta, R.3    Loupy, A.4
  • 14
    • 1442335543 scopus 로고    scopus 로고
    • Solvent-free benzylic oxidations using urea-hydrogen peroxide complex (UHP) under microwave irradiation
    • Paul, S.; Nanda, P.; Gupta, R. Solvent-free benzylic oxidations using urea-hydrogen peroxide complex (UHP) under microwave irradiation. Synlett 2004, 531-533.
    • (2004) Synlett , pp. 531-533
    • Paul, S.1    Nanda, P.2    Gupta, R.3
  • 15
    • 0347627365 scopus 로고    scopus 로고
    • Calcium acetate catalyzed synthesis of 4-arylidene-2-phenyl-5(4H)- oxazolones under solvent-free conditions
    • Paul, S.; Nanda, P.; Gupta, R.; Loupy, A. Calcium acetate catalyzed synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones under solvent-free conditions. Tetrahedron Lett. 2004, 45, 425-427.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 425-427
    • Paul, S.1    Nanda, P.2    Gupta, R.3    Loupy, A.4
  • 17
    • 0033036985 scopus 로고    scopus 로고
    • Microwave induced rate enhancement in aldol condensation
    • Kad, G. L.; Kaur, K. P.; Singh, V.; Singh, J. Microwave induced rate enhancement in aldol condensation. Synth. Commun. 1999, 29, 2583-2586.
    • (1999) Synth. Commun. , vol.29 , pp. 2583-2586
    • Kad, G.L.1    Kaur, K.P.2    Singh, V.3    Singh, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.