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Volumn 49, Issue 19, 2008, Pages 3112-3116

Direct conversion of 1-deoxy-1-nitroalditols to methyl glycofuranosides

Author keywords

1 Deoxy 1 nitroalditol; Intramolecular nucleophilic addition; Methyl glycofuranoside; Nef reaction; Nitronate; Ring closure reaction; Stereoselectivity; Walden inversion

Indexed keywords

1 DEOXY 1 NITROALDITOL DERIVATIV; 2,3 ERYTHRO METHYL GLYCOFURANOSIDE DERIVATIVE; 2,3 THREO METHYL GLYCOFURANOSIDE DERIVATIVE; ALDITOL; CARBON; CIS METHYL GLYCOFURANOSIDE DERIVATIVE; FURAN DERIVATIVE; METHYL GLYCOFURANOSIDE DERIVATIVE; NITROGEN; SODIUM DERIVATIVE; SODIUM NITRONATE; UNCLASSIFIED DRUG;

EID: 41649098131     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.03.044     Document Type: Article
Times cited : (6)

References (56)
  • 41
    • 41649112963 scopus 로고    scopus 로고
    • Vojtech, M.; Petrušová, M.; Pribulová, B.; Petruš, L. Abstracts of Papers, 14th European Carbohydrate Symposium, Lübeck, September 2007; p 262.
    • Vojtech, M.; Petrušová, M.; Pribulová, B.; Petruš, L. Abstracts of Papers, 14th European Carbohydrate Symposium, Lübeck, September 2007; p 262.
  • 49
    • 41649109818 scopus 로고    scopus 로고
    • note
    • 2O elution to yield the pure products.
  • 50
    • 41649115837 scopus 로고    scopus 로고
    • note
    • 6: C, 43.30; H, 7.27. Found: C, 43.08; H, 7.49.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.