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Volumn 72, Issue 12, 2007, Pages 4547-4550

Synthesis of α- and β-glycosyl isothiocyanates via oxazoline intermediates

Author keywords

[No Author keywords available]

Indexed keywords

ANOMERIC EFFECT; AXIAL ANOMER; ISOTHIOCYANATE;

EID: 34250166859     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062419z     Document Type: Article
Times cited : (23)

References (48)
  • 8
  • 9
    • 0032541645 scopus 로고    scopus 로고
    • (b) Taylor, C. M. Tetrahedron 1998, 54, 11317-11362.
    • (1998) Tetrahedron , vol.54 , pp. 11317-11362
    • Taylor, C.M.1
  • 14
    • 18544405939 scopus 로고    scopus 로고
    • García-Moreno, M. I.; Díaz-Pérez, P.; Ortiz, Mellet, C.; García Fernández, J. M. J. Org. Chem. 2003, 68, 8890-8901.
    • (c) García-Moreno, M. I.; Díaz-Pérez, P.; Ortiz, Mellet, C.; García Fernández, J. M. J. Org. Chem. 2003, 68, 8890-8901.
  • 22
    • 4143099312 scopus 로고    scopus 로고
    • Kohn, M.; Benito, J. M.; Ortiz, Mellet, C.; Lindhorst, T. K.; García, Fernández, J. M. ChemBioChem 2004, 5, 771-777.
    • (f) Kohn, M.; Benito, J. M.; Ortiz, Mellet, C.; Lindhorst, T. K.; García, Fernández, J. M. ChemBioChem 2004, 5, 771-777.
  • 32
    • 0028269578 scopus 로고    scopus 로고
    • Alternative approaches for the synthesis of glycosyl isothiocyanates have been reported on the basis of the addition of iodoisothiocyanate to glycals and on the phosphine imide type reaction of glycosyl azides with triphenylphosphine and carbon disulfide, yet none of these approaches allows accessing the target relative stereochemistry either. See: (a) Santoyo-González, F, García-Calvo-Flores, F, Isac-García, J, Hernández-Mateo, F, García-Mendoza, P, Robles-Díaz, R. Tetrahedron 1994, 50, 2877-2894
    • Alternative approaches for the synthesis of glycosyl isothiocyanates have been reported on the basis of the addition of iodoisothiocyanate to glycals and on the phosphine imide type reaction of glycosyl azides with triphenylphosphine and carbon disulfide, yet none of these approaches allows accessing the target relative stereochemistry either. See: (a) Santoyo-González, F.; García-Calvo-Flores, F.; Isac-García, J.; Hernández-Mateo, F.; García-Mendoza, P.; Robles-Díaz, R. Tetrahedron 1994, 50, 2877-2894.
  • 44
    • 0032847297 scopus 로고    scopus 로고
    • The propensity of N-thiocarbonylglycosylamine derivatives to undergo anomerization processes has already been demonstrated. See: Benito, J. M.; Ortiz Mellet, C.; Sadalapure, K., Lindhorst, T. K.; Defaye, J.; García Fernández, J. M. Carbohydr. Res. 1999, 320, 37-48.
    • The propensity of N-thiocarbonylglycosylamine derivatives to undergo anomerization processes has already been demonstrated. See: Benito, J. M.; Ortiz Mellet, C.; Sadalapure, K., Lindhorst, T. K.; Defaye, J.; García Fernández, J. M. Carbohydr. Res. 1999, 320, 37-48.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.