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Volumn 79, Issue C, 2009, Pages 163-194

Reactions and uses of artificial ketoses

Author keywords

Glycosidation; Ketose; Ketosidation; Ketoside; Nucleophilic Substitution

Indexed keywords


EID: 67651180889     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/REV-08-SR(D)4     Document Type: Review
Times cited : (4)

References (138)
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    • (2007) Comprehensive Glycoscience. From Chemistry to Systems Biology , vol.1-3
  • 2
    • 0004276011 scopus 로고    scopus 로고
    • Witczak Z.J., and Nieforth K.A. (Eds), Marcel Dekker, Inc., New York
    • In: Witczak Z.J., and Nieforth K.A. (Eds). Carbohydrates in Drug Design (1997), Marcel Dekker, Inc., New York
    • (1997) Carbohydrates in Drug Design
  • 3
    • 0003790195 scopus 로고    scopus 로고
    • Chapleur Y., Altenbach H.-J., Chretien F., Contelles J.M., Nicotra F., Rauter A.P., and Roberts S.M. (Eds), Wiley-VCH
    • In: Chapleur Y., Altenbach H.-J., Chretien F., Contelles J.M., Nicotra F., Rauter A.P., and Roberts S.M. (Eds). Carbohydrate Mimics. Concepts and Methods (1998), Wiley-VCH
    • (1998) Carbohydrate Mimics. Concepts and Methods
  • 4
    • 0003522385 scopus 로고
    • Levy D.E., and Tang C. (Eds), Pergamon
    • In: Levy D.E., and Tang C. (Eds). The Chemistry of C-Glycosides (1995), Pergamon
    • (1995) The Chemistry of C-Glycosides
  • 116
    • 67651198775 scopus 로고    scopus 로고
    • note
    • 2O gave the open ring compound. See ref. 32.
  • 117
    • 34547816059 scopus 로고    scopus 로고
    • 3 was also successfully applicable to the O-ketosidation of D-fructofuranose derivatives
    • 3 was also successfully applicable to the O-ketosidation of D-fructofuranose derivatives. Yamanoi T., Misawa N., and Watanabe M. Tetrahedron Lett. 48 (2007) 6458
    • (2007) Tetrahedron Lett. , vol.48 , pp. 6458
    • Yamanoi, T.1    Misawa, N.2    Watanabe, M.3
  • 129
    • 38949216070 scopus 로고    scopus 로고
    • 3 was effectively catalyzed the glcosidaton using 1-hydroxy sugars
    • 3 was effectively catalyzed the glcosidaton using 1-hydroxy sugars. Yamanoi T., Inoue R., Matsuda S., and Hamasaki K. Lett. Org. Chem. 5 (2008) 30
    • (2008) Lett. Org. Chem. , vol.5 , pp. 30
    • Yamanoi, T.1    Inoue, R.2    Matsuda, S.3    Hamasaki, K.4
  • 131
    • 67651179313 scopus 로고    scopus 로고
    • note
    • A similar paper was reported. See ref. 15.
  • 135
    • 0037131158 scopus 로고    scopus 로고
    • Other synthetic approaches to an anhydro-D-altro-heptulose were as follows
    • Other synthetic approaches to an anhydro-D-altro-heptulose were as follows. Francisco C.G., Herrera A.J., and Suárez E. J. Org. Chem. 67 (2002) 7439
    • (2002) J. Org. Chem. , vol.67 , pp. 7439
    • Francisco, C.G.1    Herrera, A.J.2    Suárez, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.