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Volumn 46, Issue 16, 2005, Pages 2839-2843

Amino acid-catalyzed direct enantioselective synthesis of β-amino-α-oxyaldehydes

Author keywords

Amino sugars; Asymmetric catalysis; Mannich reaction; Proline derivatives; Oxyaldehydes

Indexed keywords

ALDEHYDE DERIVATIVE; AMINO ACID;

EID: 15944403573     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.02.116     Document Type: Article
Times cited : (71)

References (77)
  • 38
  • 73
    • 85030807947 scopus 로고    scopus 로고
    • note
    • +: calcd 430.1994)
  • 74
    • 85030816933 scopus 로고    scopus 로고
    • note
    • The compounds are sensitive and they epimerize and racemize upon silica-gel column chromatography. The β-amino-α-oxyaldehyde products should be stored at -35°C
  • 75
    • 85030812699 scopus 로고    scopus 로고
    • note
    • 11a,11b
  • 76
    • 21844482982 scopus 로고
    • Protected amino alcohol 1a was converted to the known peracetylated (2R,3S)-2-aminothreitol with [ α ] D 24 + 40 (c = 0.1, MeOH). The reported optical rotation for peracetylated (2R,3S)-aminothreitol is [ α ] D 25 + 40.3 (c = 1.12, MeOH) P.A. Wade, and S.G. D'Ambrosio J. Carbohydr. Chem. 14 1995 1329
    • (1995) J. Carbohydr. Chem. , vol.14 , pp. 1329
    • Wade, P.A.1    D'Ambrosio, S.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.