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Volumn 38, Issue 46, 1997, Pages 7977-7980

Synthesis of carbohydrate mimics: α-1-C-substituted-deoxymannojirimycins

Author keywords

[No Author keywords available]

Indexed keywords

1 DEOXYMANNONOJIRIMYCIN; 1 DEOXYMANNONOJIRIMYCIN DERIVATIVE; GLYCOSIDASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 0030727057     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)10144-7     Document Type: Article
Times cited : (9)

References (26)
  • 16
    • 0029990596 scopus 로고    scopus 로고
    • For a recent report of a C-glycoside with the α-manno configuration used as a M. tuberculosis inhibitor see For α-manno mimics of Sialyl Lewis X see
    • For a recent report of a C-glycoside with the α-manno configuration used as a M. tuberculosis inhibitor see Jarreton, O.; Skrydstrup, T.; Beau, J.-M. J. Chem. Soc. Chem. Commun. 1996, 1661. For α-manno mimics of Sialyl Lewis X see Marron, T.G.; Woltering, T.J.; Weitz-Schmidt, G.; Wong, C.-H. Tetrahedron Lett. 1996, 37, 9037.
    • (1996) J. Chem. Soc. Chem. Commun. , pp. 1661
    • Jarreton, O.1    Skrydstrup, T.2    Beau, J.-M.3
  • 17
    • 0030577494 scopus 로고    scopus 로고
    • For a recent report of a C-glycoside with the α-manno configuration used as a M. tuberculosis inhibitor see Jarreton, O.; Skrydstrup, T.; Beau, J.-M. J. Chem. Soc. Chem. Commun. 1996, 1661. For α-manno mimics of Sialyl Lewis X see Marron, T.G.; Woltering, T.J.; Weitz-Schmidt, G.; Wong, C.-H. Tetrahedron Lett. 1996, 37, 9037.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 9037
    • Marron, T.G.1    Woltering, T.J.2    Weitz-Schmidt, G.3    Wong, C.-H.4
  • 18
    • 0001854467 scopus 로고    scopus 로고
    • The diol derived from bromobenzene is now prepared in crystalline form on a multikilogram scale by Genecor International, Inc., Rochester, NY. For a nice overview of applications of such cis-cyclohexadienediols see
    • The diol derived from bromobenzene is now prepared in crystalline form on a multikilogram scale by Genecor International, Inc., Rochester, NY. For a nice overview of applications of such cis-cyclohexadienediols see Hudlickly, T.; Thorpe, A.J. J. Chem. Soc. Chem. Commun. 1996, 1993.
    • (1996) J. Chem. Soc. Chem. Commun. , pp. 1993
    • Hudlickly, T.1    Thorpe, A.J.2
  • 23
    • 0343193948 scopus 로고    scopus 로고
    • All compounds reported above have been fully characterized. For data see Ph.D. Dissertation, Wayne State University
    • All compounds reported above have been fully characterized. For data see Johns, B.A. Ph.D. Dissertation, Wayne State University, 1997.
    • (1997)
    • Johns, B.A.1
  • 24
    • 0027210821 scopus 로고
    • Ring closure during mesylation has been reported for similar cases see
    • Ring closure during mesylation has been reported for similar cases see Bonnaud, B.; Bigg, D.C.H. J. Heterocyclic Chem. 1993, 30, 505.
    • (1993) J. Heterocyclic Chem. , vol.30 , pp. 505
    • Bonnaud, B.1    Bigg, D.C.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.