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Volumn 36, Issue 5, 1995, Pages 653-654

Synthesis of (+)-1-deoxygalactonojirimycin and a related indolizidine

Author keywords

[No Author keywords available]

Indexed keywords

1 DEOXYGALACTONOJIRIMYCIN; INDOLIZIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0028831989     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(94)02343-A     Document Type: Article
Times cited : (68)

References (29)
  • 6
    • 1842310465 scopus 로고
    • Inhibitors of the Addition, Modification or Processing of the Oligosaccharide Chains of the N-Linked Glycoproteins
    • V. Ginsberg, P.W. Robbins, JAI Press, London
    • (1991) Biology of Carbohydrates , vol.3 , pp. 119
    • Elbein1
  • 11
    • 84982074684 scopus 로고
    • Monosaccharide mit stickstoffhaltigem Ring, XXXVII. Synthese von 1,5-Didesoxy-1,5-imino-D-galactit
    • For previous syntheses of galactonojirimycin and its analogs see:
    • (1980) Chemische Berichte , vol.113 , pp. 2601
    • Paulsen1    Hayauchi2    Sinnwell3
  • 18
    • 84987474619 scopus 로고
    • Enantioselective Syntheses of Conduramines from Benzene by Microbial Oxidation, Enzymatic Asymmetrization and Resolution in Organic Media
    • (1992) Synlett , pp. 388
    • Johnson1    Ple2    Su3    Heeg4    Adams5
  • 22
    • 84986370146 scopus 로고
    • Enantiomerenreine Pyrrolidin-Derivate austrans-4-Hydroxy-L-prolin durch elektrochemische oxidative Decarboxylierung und Titantetrachlorid-vermittelte Umsetzung mit Nukleophilen
    • (1986) Helvetica Chimica Acta , vol.69 , pp. 1704
    • Renaud1    Seebach2
  • 24
    • 84980158220 scopus 로고
    • A Convenient One-Flask Synthesis of 1-Methylazetidines from 3-Aminoalkanols, Triphenylphosphine, and Carbon Tetrachloride
    • (1979) Synthesis , pp. 105
    • Stoilova1    Trifonov2    Orahovats3
  • 28
    • 84915386225 scopus 로고    scopus 로고
    • 3, 300 MHz) δ: 4.28 (m, 2H); 4.06 (m, 3H); 3.90 (ddd, J= 5.9, 1.7, 1.7 Hz, 1H); 3.78 (dd, J= 11.6, 6.0 Hz, 1H); 3.53 (m, 1H); 3.44 (dd, J=4.0, 4.0 Hz, 1H); 2.40-2.00 (m, 4H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.