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Volumn 347, Issue 4, 2005, Pages 555-562

Base-catalyzed condensation of 2-hydroxybenzaldehydes with α,β-unsaturated aldehydes - Scope and limitations

Author keywords

aldol reaction; Enols; Enones; Nucleophilic addition; Oxygen heterocycles

Indexed keywords

ALDEHYDE DERIVATIVE; BASE; CARBONYL DERIVATIVE; DIENESTROL; DIHYDROBENZOFURAN DERIVATIVE; SALICYLALDEHYDE; XANTHONE DERIVATIVE;

EID: 17144390227     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200404239     Document Type: Article
Times cited : (79)

References (43)
  • 1
    • 37049102896 scopus 로고
    • 9-THC: d) Y. Gaoni, R. Mechoulam, J. Am. Chem. Soc. 1964, 86, 1646-1647; e) A. C. Hewlett, F. Barth, T. I. Bonner, G. Cabral, P. Casellas, W. A. Devane, C. C. Felder, M. Herkenham, K. Mackie, B. R. Martin, R. Mechoulam, R. G. Pertwee, Pharmacol. Rev. 2002, 54, 161-202, and literature cited therein.
    • (1977) J. Chem. Soc. Perkin Trans. 1 , pp. 405-410
    • Manners, G.D.1    Jurd, L.2
  • 3
    • 0033799436 scopus 로고    scopus 로고
    • 9-THC: d) Y. Gaoni, R. Mechoulam, J. Am. Chem. Soc. 1964, 86, 1646-1647; e) A. C. Hewlett, F. Barth, T. I. Bonner, G. Cabral, P. Casellas, W. A. Devane, C. C. Felder, M. Herkenham, K. Mackie, B. R. Martin, R. Mechoulam, R. G. Pertwee, Pharmacol. Rev. 2002, 54, 161-202, and literature cited therein.
    • (2000) Eur. J. Org. Chem. , pp. 3223-3228
    • Bouzbouz, S.1    Goujon, J.-Y.2    Deplanne, J.3    Kirschleger, B.4
  • 4
    • 33947489961 scopus 로고
    • 9-THC: d) Y. Gaoni, R. Mechoulam, J. Am. Chem. Soc. 1964, 86, 1646-1647; e) A. C. Hewlett, F. Barth, T. I. Bonner, G. Cabral, P. Casellas, W. A. Devane, C. C. Felder, M. Herkenham, K. Mackie, B. R. Martin, R. Mechoulam, R. G. Pertwee, Pharmacol. Rev. 2002, 54, 161-202, and literature cited therein.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 1646-1647
    • Gaoni, Y.1    Mechoulam, R.2
  • 6
    • 4243830773 scopus 로고
    • German Patent DE-B 2155113, 1972
    • a) A. B. Baylis, M. E. D. Hillman, German Patent DE-B 2155113, 1972; Chem. Abstr. 1972, 77, 34174q;
    • (1972) Chem. Abstr. , vol.77
    • Baylis, A.B.1    Hillman, M.E.D.2
  • 15
    • 4644270942 scopus 로고    scopus 로고
    • B. Lesch, S. Bräse, Angew. Chem. 2004, 116, 118-120; Angew. Chem. Int. Ed. 2004, 43, 115-118.
    • (2004) Angew. Chem. , vol.116 , pp. 118-120
    • Lesch, B.1    Bräse, S.2
  • 16
    • 2942696621 scopus 로고    scopus 로고
    • B. Lesch, S. Bräse, Angew. Chem. 2004, 116, 118-120; Angew. Chem. Int. Ed. 2004, 43, 115-118.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 115-118
  • 18
    • 17144432013 scopus 로고    scopus 로고
    • note
    • A full account of this work is in preparation.
  • 32
    • 17144373444 scopus 로고    scopus 로고
    • note
    • All experimental data are available as supplemental material.
  • 33
    • 0003467672 scopus 로고
    • John Wiley & Sons, New York
    • a values can be found at http://daecr1.harvard.edu/ pdf/evans_pKa_ table.pdf.
    • (1985) rd Edn.
    • March, J.1
  • 35
    • 17144381793 scopus 로고    scopus 로고
    • note
    • Calculated using Advanced Chemistry Development (ACD) Software Solaris V4.76 implemented in CAS Scifinder.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.