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Volumn , Issue 5, 2000, Pages 787-797

A novel method for the synthesis of substituted naphthalenes and phenanthrenes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; MERCURY VAPOR LAMPS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL);

EID: 0034615524     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/a908361h     Document Type: Article
Times cited : (72)

References (54)
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    • General reviews on the synthesis of naphthalenes and phenanthrenes:
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    • (1992) The Total Synthesis of Natural Products , vol.8 , pp. 311-531
    • Thomson, R.H.1
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    • ed. R. H. Thomson, Blackie, Glasgow and London
    • (b) T. J. Simpson, in The Chemistry of Natural Products, ed. R. H. Thomson, Blackie, Glasgow and London, 1985, pp. 107-153;
    • (1985) The Chemistry of Natural Products , pp. 107-153
    • Simpson, T.J.1
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    • ed. R. H. Thomson, Blackie Academic and Professional, London, 2nd edn.
    • M. Gill, in The Chemistry of Natural Products, ed. R. H. Thomson, Blackie Academic and Professional, London, 2nd edn., 1993, pp. 60-105;
    • (1993) The Chemistry of Natural Products , pp. 60-105
    • Gill, M.1
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    • 0011235163 scopus 로고
    • ed. J. ApSimon, John Wiley & Sons Inc., New York
    • (b) R. H. Thomson, in The Total Synthesis of Natural Products, ed. J. ApSimon, John Wiley & Sons Inc., New York, 1992, vol. 8, p. 330;
    • (1992) The Total Synthesis of Natural Products , vol.8 , pp. 330
    • Thomson, R.H.1
  • 17
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    • ed. J. F. Stoddart, Pergamon Press Ltd., Oxford
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    • (1979) Comprehensive Organic Chemistry , vol.1 , pp. 166
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    • 7 has suggested that cyclobutanols may be possible intermediates in the course of their reaction resulting in the formation of naphthols, but we did not isolate this type of intermediate
    • 7 has suggested that cyclobutanols may be possible intermediates in the course of their reaction resulting in the formation of naphthols, but we did not isolate this type of intermediate.
  • 34
    • 0001786881 scopus 로고    scopus 로고
    • ed. F. Diederich and P. J. Stang, Wiley-VCH, Weinheim
    • (c) A. Suzuki, in MetalCatalyzed Cross-Coupling Reactions, ed. F. Diederich and P. J. Stang, Wiley-VCH, Weinheim, 1998, pp. 49-97;
    • (1998) MetalCatalyzed Cross-Coupling Reactions , pp. 49-97
    • Suzuki, A.1
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    • 33645918081 scopus 로고    scopus 로고
    • The aromatic bromide 30 is commercially available. Compound 31 was prepared by treatment of isovanillin with bromine in acetic acid followed by methylation with dimethyl sulfate in the presence of potassium carbonate and DMF.
    • The aromatic bromide 30 is commercially available. Compound 31 was prepared by treatment of isovanillin with bromine in acetic acid followed by methylation with dimethyl sulfate in the presence of potassium carbonate and DMF.
  • 40
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    • (1997) Chem. Abstr. , vol.126 , pp. 8006
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    • WO 9 840 331
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    • (Chem. Abstr., 1999, 129, 260575v).
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    • Other syntheses of Tanshinone I
    • Other syntheses of Tanshinone I:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.