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Volumn , Issue 3, 2004, Pages 546-548

Stereospecific Construction of Chiral Quaternary α-Oxygenated Aldehydes from Chiral Secondary Alcohol Derivatives

Author keywords

Chiral synthesis; Methoxide anion; Ring opening; , disubstituted oxyaldehyde; chloroepoxide

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE DERIVATIVE; EPOXIDE; METHANOL; POTASSIUM CYANIDE;

EID: 1442360066     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-815406     Document Type: Article
Times cited : (12)

References (27)
  • 1
    • 0001521888 scopus 로고
    • (a) Fuji, K. Chem. Rev. 1993, 93, 2037.
    • (1993) Chem. Rev. , vol.93 , pp. 2037
    • Fuji, K.1
  • 8
    • 0034536438 scopus 로고    scopus 로고
    • and references cited therein
    • (e) Frohn, M.; Shi, Y. Synthesis 2000, 1979; and references cited therein.
    • (2000) Synthesis , pp. 1979
    • Frohn, M.1    Shi, Y.2
  • 17
    • 1442343368 scopus 로고    scopus 로고
    • note
    • Chiral HPLC was performed on CHIRALCEL OJ for 7 and 11 using a solvent system of hexane/i-PrOH (500/1 or 200/1). These compounds analyzed were determined to be >98% ee, which stands for no detection of the other enantiomer.
  • 18
    • 1442318899 scopus 로고    scopus 로고
    • note
    • (a) The reagent AD-Mix-β was purchased from Aldrich Com. The glycol 9 proved to be obtained in 72% ee from chiral HPLC of the derived 7 using CHIRALCEL OJ (hexane/i-PrOH = 500/1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.