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Volumn 33, Issue 4, 2003, Pages 527-533

A convenient method for the synthesis of dehydroquinic acid

Author keywords

Dehydroquinic acid; Selective protection; Shikimate pathway; Synthesis

Indexed keywords

HYDROXYACID;

EID: 0037236748     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120015805     Document Type: Article
Times cited : (8)

References (12)
  • 1
    • 0000439082 scopus 로고    scopus 로고
    • Enzymology and molecular biology of the shikimate pathway
    • Sankawa, U., Ed.; Elsevier: Amsterdam, 573-607pp
    • Abell, C. Enzymology and molecular biology of the shikimate pathway. Comprehensive Natural Product Chemistry; Sankawa, U., Ed.; Elsevier: Amsterdam, 1999; 573-607pp.
    • (1999) Comprehensive Natural Product Chemistry
    • Abell, C.1
  • 2
    • 0033406039 scopus 로고    scopus 로고
    • Synthesis of 3-deoxy-3,3-difluoroshikimic acid and its 4-epimer from quinic acid
    • Jiang, S.; Singh, G.; Boam, D.J.; Coggins, J.R. Synthesis of 3-deoxy-3,3-difluoroshikimic acid and its 4-epimer from quinic acid. Tetrahedron: Asymmetry 1999, 10, 4087.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 4087
    • Jiang, S.1    Singh, G.2    Boam, D.J.3    Coggins, J.R.4
  • 4
    • 0036026237 scopus 로고    scopus 로고
    • A simple method for the preparation of 3-hydroxyiminodehydroquinate, a potent inhibitor of type II dehydroquinase
    • Le Sann, C.; Abell, C.; Abell, A.D. A simple method for the preparation of 3-hydroxyiminodehydroquinate, a potent inhibitor of type II dehydroquinase, J. Chem. Soc., Perkin Trans. 1, 2002, 2065.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 2065
    • Le Sann, C.1    Abell, C.2    Abell, A.D.3
  • 5
    • 4344560998 scopus 로고
    • The preparation and identification of 5-dehydroquinic and 5-dehydroshikimic acids
    • Haslam, E.; Haworth, R.D.; Knowles, P.F. The preparation and identification of 5-dehydroquinic and 5-dehydroshikimic acids. Methods in Enzymology 1956, 499.
    • (1956) Methods in Enzymology , pp. 499
    • Haslam, E.1    Haworth, R.D.2    Knowles, P.F.3
  • 6
    • 37049135086 scopus 로고
    • The shikimate pathway - Part I. Introduction. Preparation of stereospecifically labelled 2-deuterio-derivatives of 3-dehydroquinic acid
    • Haslam, E.; Turner, M.J.; Sargent, D.; Thompson, R.S. The shikimate pathway - Part I. Introduction. Preparation of stereospecifically labelled 2-deuterio-derivatives of 3-dehydroquinic acid. J. Chem. Soc. 1971, 1489.
    • (1971) J. Chem. Soc. , pp. 1489
    • Haslam, E.1    Turner, M.J.2    Sargent, D.3    Thompson, R.S.4
  • 7
    • 33750364100 scopus 로고
    • Die Synthese der dehydro-chinasäure
    • Grewe, R.; Jeschke, J.P. Die Synthese der dehydro-chinasäure. Chem. Ber. 1956, 89, 2080.
    • (1956) Chem. Ber. , vol.89 , pp. 2080
    • Grewe, R.1    Jeschke, J.P.2
  • 10
    • 0034605826 scopus 로고    scopus 로고
    • Efficient synthesis of (-)-methyl 3-epi-shikimate and methyl 3-epi-quinate by one-pot selective protection of trans-1,2-diols
    • Armesto, N.; Ferrero, M.; Fernandez, S.; Gotor, V. Efficient synthesis of (-)-methyl 3-epi-shikimate and methyl 3-epi-quinate by one-pot selective protection of trans-1,2-diols. Tetrahedron Letters 2000, 41, 8759.
    • (2000) Tetrahedron Letters , vol.41 , pp. 8759
    • Armesto, N.1    Ferrero, M.2    Fernandez, S.3    Gotor, V.4
  • 11
    • 0033538623 scopus 로고    scopus 로고
    • An efficient transformation of quinic acid to shikimic acid derivatives
    • Alves, C.; Barros, M.T.; Maycock, C.D.; Ventura, M.R. An efficient transformation of quinic acid to shikimic acid derivatives. Tetrahedron 1999, 55, 8443.
    • (1999) Tetrahedron , vol.55 , pp. 8443
    • Alves, C.1    Barros, M.T.2    Maycock, C.D.3    Ventura, M.R.4
  • 12
    • 84985644071 scopus 로고
    • Hetero Diels-Alder reactions of allenes on silica gel and under liquid-phase conditions
    • Conrads, M.; Mattay, J.; Runsink, Hetero Diels-Alder reactions of allenes on silica gel and under liquid-phase conditions. J. Chem. Ber. 1989, 122, 2207.
    • (1989) J. Chem. Ber. , vol.122 , pp. 2207
    • Conrads, M.1    Mattay, J.2    Runsink3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.