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Volumn 60, Issue 38, 2004, Pages 8295-8328

Synthetic approaches to 2-tetralones

Author keywords

2 Tetralones; Friedel Crafts; Indanones; Lewis acids; Synthesis; Tetralines

Indexed keywords

ACETYLENE DERIVATIVE; ALCOHOL; ALKENE DERIVATIVE; AMMONIA; AZO COMPOUND; BENZENE DERIVATIVE; CARBONYL DERIVATIVE; CERIUM; COPPER CHLORIDE; EPOXIDE; ETHER DERIVATIVE; IMINE; KETONE DERIVATIVE; MANGANESE; NAPHTHALENE DERIVATIVE; NAPHTHOL DERIVATIVE; PALLADIUM; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; RUTHENIUM COMPLEX; SODIUM; SULFOXIDE; TETRALIN DERIVATIVE; VINYL DERIVATIVE;

EID: 4444359839     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.06.080     Document Type: Review
Times cited : (34)

References (305)
  • 36
    • 85028739478 scopus 로고
    • Zinke T. Chem. Ber. 21:1888;3540-3559
    • (1888) Chem. Ber. , vol.21 , pp. 3540-3559
    • Zinke, T.1
  • 38
    • 4444237138 scopus 로고
    • For examples of 2-tetralones as key intermediates in the synthesis of compounds with pharmacological activities, see: (a)
    • For examples of 2-tetralones as key intermediates in the synthesis of compounds with pharmacological activities, see: (a) Horii Z., Watanabe T., Kurihara T., Tamura Y. Chem. Pharm. Bull. 13:1965;420-426
    • (1965) Chem. Pharm. Bull. , vol.13 , pp. 420-426
    • Horii, Z.1    Watanabe, T.2    Kurihara, T.3    Tamura, Y.4
  • 42
    • 0028787293 scopus 로고
    • For examples of 2-tetralones as key intermediates for the preparation of bioactive compounds, see: (a)
    • For examples of 2-tetralones as key intermediates for the preparation of bioactive compounds, see: (a) Chumpradit S., Kung M.-P., Vessotskie J., Kung H.F. J. Labelled Compd. Radiopharm. 36:1995;1051-1062
    • (1995) J. Labelled Compd. Radiopharm. , vol.36 , pp. 1051-1062
    • Chumpradit, S.1    Kung, M.-P.2    Vessotskie, J.3    Kung, H.F.4
  • 61
    • 0003394220 scopus 로고
    • (b) For a review of intramolecular addition of diazoketones to aromatic systems, see: M.P. Doyle, M.A. McKervey, & T. Ye. New York: Wiley
    • (b) For a review of intramolecular addition of diazoketones to aromatic systems, see: Doyle M.P., McKervey M.A., Ye T. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds. 1988;298-336 Wiley, New York
    • (1988) Modern Catalytic Methods for Organic Synthesis with Diazo Compounds , pp. 298-336
  • 207
    • 0000022346 scopus 로고
    • For reviews on carbonyl transposition strategies, see: (a)
    • For reviews on carbonyl transposition strategies, see: (a) Kane V.V., Singh V., Martin A. Tetrahedron. 39:1983;345-394
    • (1983) Tetrahedron , vol.39 , pp. 345-394
    • Kane, V.V.1    Singh, V.2    Martin, A.3
  • 209
    • 0001312924 scopus 로고
    • Trost B.M. Oxford: Pergamon. Chapter 3.3
    • Rickborn B. Trost B.M. Comprehensive Organic Synthesis. Vol. 3:1991;733-775 Pergamon, Oxford. Chapter 3.3
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 733-775
    • Rickborn, B.1
  • 297
    • 4444283331 scopus 로고    scopus 로고
    • Eur. Pat. Appl. 0378456, 1990.
    • (b) D'Orchymont, H.; Tarnus, C. Eur. Pat. Appl. 0378456, 1990.
    • D'Orchymont, H.1    Tarnus, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.