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Volumn 39, Issue 24, 1998, Pages 4305-4308

Asymmetric nucleophilic addition to β-and γ-alkoxy aldehydes using carbohydrate as a chiral auxiliary

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE DERIVATIVE; ARABINOSE; BUTYRALDEHYDE; CARBOHYDRATE; FUCOSE; PROPIONALDEHYDE; REAGENT; TETRAHYDROPYRAN DERIVATIVE; TRIBUTYLTIN;

EID: 0032507927     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00717-5     Document Type: Article
Times cited : (12)

References (23)
  • 3
    • 0010771837 scopus 로고
    • (c) Review of chelation-controlled addition reaction to α - and β-alkoxy carbonyl compounds: Reetz, T. M. Angew. Chem. Int. Ed. Engl. 1984, 23, 556
    • (1984) Angew. Chem. Int. Ed. Engl. , vol.23 , pp. 556
    • Reetz, T.M.1
  • 11
    • 84920313082 scopus 로고    scopus 로고
    • note
    • 5. Without MS 4A, addition reactions resulted in decreased yields.
  • 12
    • 84920313081 scopus 로고    scopus 로고
    • note
    • 6. In the addition of PhMgBr to δ-alkoxy aldehyde (n=4), the corresponding alcohol was obtained with 30% de by 1,7-asymmetric induction.
  • 13
    • 84920313080 scopus 로고    scopus 로고
    • note
    • 2 lowered the diastereoselectivity.
  • 20
    • 84920313079 scopus 로고    scopus 로고
    • note
    • 2 2:1 complex may be reformed quickly after the addition to one of the aldehydes.
  • 21
    • 84920313078 scopus 로고    scopus 로고
    • note
    • 2c. (Equation Presented)
  • 23
    • 84920313077 scopus 로고    scopus 로고
    • note
    • 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.