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Volumn 4, Issue 19, 2002, Pages 3321-3324

Development of a rapid, room-temperature dynamic kinetic resolution for efficient asymmetric synthesis of α-aryl amino acids

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID;

EID: 0037136494     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026660l     Document Type: Article
Times cited : (68)

References (37)
  • 30
    • 0001660358 scopus 로고    scopus 로고
    • For a study of dynamic kinetic resolutions of azlactones, see: Liang, J.; Ruble, J. C.; Fu, G. C. J. Org. Chem. 1998, 63, 3154.
    • (1998) J. Org. Chem. , vol.63 , pp. 3154
    • Liang, J.1    Ruble, J.C.2    Fu, G.C.3
  • 33
    • 0041816977 scopus 로고    scopus 로고
    • For a catalytic asymmetric synthesis of 3-pyridylglycine, see ref 5
    • For a catalytic asymmetric synthesis of 3-pyridylglycine, see ref 5.
  • 34
    • 0033023975 scopus 로고    scopus 로고
    • Review of recent approaches of using transition-metal-enzyme combinations to effect fast racemization required for efficient kinetic resolutions: El Gihani, M. T.; Williams, J. M. J. Curr. Opin. Chem. Biol. 1999, 3, 11.
    • (1999) J. Curr. Opin. Chem. Biol. , vol.3 , pp. 11
    • El Gihani, M.T.1    Williams, J.M.2
  • 37
    • 0041816978 scopus 로고    scopus 로고
    • Buchwald and co-workers observed that the efficiency of the dynamic kinetic resolution of 3,5-dialkyl cyclopentenones can be improved by increasing the reaction temperature, presumably via acceleration of the racemization relative to the enantioselective transformation of 3,5-dialkyl cyclopentenones; see ref 10(a)
    • Buchwald and co-workers observed that the efficiency of the dynamic kinetic resolution of 3,5-dialkyl cyclopentenones can be improved by increasing the reaction temperature, presumably via acceleration of the racemization relative to the enantioselective transformation of 3,5-dialkyl cyclopentenones; see ref 10(a).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.