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Volumn 54, Issue 48, 1998, Pages 14549-14564

Asymmetric reactions of α-ketoacid-derived hemiacetals: Stereoselective synthesis of α-hydroxy acids

Author keywords

Asymmetric reactions; Grignard reactions; Hydroxy acids

Indexed keywords

2 OXOACID; ACETAL DERIVATIVE; HYDROXYACID;

EID: 0032569892     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00914-4     Document Type: Article
Times cited : (20)

References (28)
  • 5
    • 0029032614 scopus 로고
    • [5] For leading references, see: Byun, I. S.; Kim, Y. H. Syn. Comm. 1995;25:1963.
    • (1995) Syn. Comm. , vol.25 , pp. 1963
    • Byun, I.S.1    Kim, Y.H.2
  • 8
    • 0000227799 scopus 로고
    • This study is the sole example of an intramolecular reduction of an α-keto ester in an NADH mimicking system
    • [8] Meyers, A. I.; Brown, J. D. J. Am. Chem. Soc. 1987;109:3155. This study is the sole example of an intramolecular reduction of an α-keto ester in an NADH mimicking system.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 3155
    • Meyers, A.I.1    Brown, J.D.2
  • 19
    • 37049093317 scopus 로고
    • [19] Eight membered transition structures have been invoked earlier in reduction with sodium cyanaborohydride, see: Takano, S.; Otaki, S.; Ogasawara, K. J. Chem. Commun. 1983;1172.
    • (1983) J. Chem. Commun. , pp. 1172
    • Takano, S.1    Otaki, S.2    Ogasawara, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.