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Volumn , Issue 10, 2005, Pages 1547-1550

A divergent synthesis of uncommon sugars from furanaldehyde

Author keywords

1 (2 furyl)ethanol; Achmatowicz rearrangement; Enzymatic kinetic resolution; Uncommon sugar

Indexed keywords

1 (2 FURYL)ETHANOL; ALCOHOL; ALDEHYDE DERIVATIVE; FURANALDEHYDE; LACTONE; SUGAR; UNCLASSIFIED DRUG;

EID: 21544450028     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-869846     Document Type: Article
Times cited : (24)

References (42)
  • 14
    • 84943842705 scopus 로고
    • and references cited therein
    • (a) For a comprehensive review based on stereoselective syntheses of carbohydrates, see: McGarvey, G. J.; Kimura, M.; Oh, T.; Williams, J. M. J. Carbohydr. Chem. 1984, 3, 125; and references cited therein,
    • (1984) J. Carbohydr. Chem. , vol.3 , pp. 125
    • McGarvey, G.J.1    Kimura, M.2    Oh, T.3    Williams, J.M.4
  • 36
    • 21544434871 scopus 로고    scopus 로고
    • note
    • 4Cl complex (3-4 equiv).
  • 37
    • 21544473790 scopus 로고    scopus 로고
    • note
    • Compound 4 is not very stable, after reaction it should be used directly. Storage at 4 °C for 3 d led to decomposition to a black oil.
  • 42
    • 21544466663 scopus 로고    scopus 로고
    • note
    • 4 and concentrated under vacuum. The crude product was purified by column chromatography (hexanes-EtOAc, 10:1) to give (R)-1 (21.5 g, >97% ee by chiral GC analysis).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.