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Volumn , Issue SPEC. ISS., 1999, Pages 885-888

Syntheses of the D-aldopentoses from non-carbohydrate sources

Author keywords

1,2 diol cleavage; Cis 1,2 dihydrocatechol; D xylose; D arabinose; D lyxono lactone; D lyxose; D ribose; Ozonolytic cleavage; Radical decarboxylation

Indexed keywords

PENTOSE;

EID: 0033044198     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3179     Document Type: Article
Times cited : (16)

References (56)
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    • Hudlicky, T.; Price, J. D. Synlett, 1990, 159. For an excellent discussion of the potential of compounds of the type 5-7 as starting materials for the synthesis of variou s monosaccharides see: Hudlicky, T.; Reed, J. A. In Advances in Asymmetric Synthesis; Hassner, A. Ed.; JAI: Greenwich, CT, 1995; 1, p 271.
    • (1990) Synlett , pp. 159
    • Hudlicky, T.1    Price, J.D.2
  • 28
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    • Hassner, A. Ed.; JAI: Greenwich, CT
    • Hudlicky, T.; Price, J. D. Synlett, 1990, 159. For an excellent discussion of the potential of compounds of the type 5-7 as starting materials for the synthesis of variou s monosaccharides see: Hudlicky, T.; Reed, J. A. In Advances in Asymmetric Synthesis; Hassner, A. Ed.; JAI: Greenwich, CT, 1995; 1, p 271.
    • (1995) Advances in Asymmetric Synthesis , vol.1 , pp. 271
    • Hudlicky, T.1    Reed, J.A.2
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    • and references cited there-in
    • See Zylstra, G. J.; Gibson, D. T. J. Biol. Chem., 1989, 264, 14940 and references cited there-in.
    • (1989) J. Biol. Chem. , vol.264 , pp. 14940
    • Zylstra, G.J.1    Gibson, D.T.2
  • 30
    • 0001854468 scopus 로고    scopus 로고
    • For a concise review on the applications of cis-1,2-dihydrocatechols in synthesis see Hudlicky, T.; Thorpe, A. J. Chem. Commun., 1996, 1993.
    • (1996) Chem. Commun. , pp. 1993
    • Hudlicky, T.1    Thorpe, A.J.2
  • 32
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    • note
    • 3 at 20 °C.
  • 33
    • 0016842206 scopus 로고
    • This type of ozonolytic cleavage of cyclic enones has been described previously (Chavdarian, C. G.; Heathcock, C. H. J. Org. Chem., 1975, 40, 2970). For related cleavages that do not involve a reductive "work-up" see Cella, J. A., Synth. Commun., 1983, 13, 93.
    • (1975) J. Org. Chem. , vol.40 , pp. 2970
    • Chavdarian, C.G.1    Heathcock, C.H.2
  • 34
    • 0002001420 scopus 로고
    • This type of ozonolytic cleavage of cyclic enones has been described previously (Chavdarian, C. G.; Heathcock, C. H. J. Org. Chem., 1975, 40, 2970). For related cleavages that do not involve a reductive "work-up" see Cella, J. A., Synth. Commun., 1983, 13, 93.
    • (1983) Synth. Commun. , vol.13 , pp. 93
    • Cella, J.A.1
  • 38
    • 0344766037 scopus 로고    scopus 로고
    • note
    • Crystal structure data have been deposited with the Cambridge Crystallographic Data Centre (CCDC) and can be obtained by directing enquiries to the following address: The Director, CCDC, 12 Union Road, Cambridge, CB2 1EZ, United Kingdom.
  • 48
  • 53
    • 85087574934 scopus 로고    scopus 로고
    • note
    • 25a for the synthesis of the corresponding L-enantiomer (from L-xylose).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.