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Volumn 50, Issue 34, 2009, Pages 4941-4944

Preparation of all stereoisomers of 2-allyl-2-methyl-3-hydroxycyclopentanone by desymmetric processes based on a microbial oxidation and reduction system

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANONE DERIVATIVE; CYCLOPENTANONE DERIVATIVE; DIKETONE;

EID: 67649867179     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.06.080     Document Type: Article
Times cited : (8)

References (30)
  • 21
    • 67649833524 scopus 로고    scopus 로고
    • Roberts S.M., and Ehittall J. (Eds), John Wiley, New York
    • Nakamura K., Fujii M., and Ida Y. In: Roberts S.M., and Ehittall J. (Eds). Asymmetric Reduction of Ketones: Synthesis of Both Enantiomers of 1-Phenylethanol by Reduction of Acetophenone with Geotrichum candidum IFO 5767. Catalysts for Fine Chemical Synthesis Vol. 5 (2007), John Wiley, New York 93-97
    • (2007) Catalysts for Fine Chemical Synthesis , vol.5 , pp. 93-97
    • Nakamura, K.1    Fujii, M.2    Ida, Y.3
  • 24
    • 67649872131 scopus 로고    scopus 로고
    • note
    • 2: C, 70.10; H, 9.15. Found: C, 69.89; H. 9.15.
  • 25
    • 67649856356 scopus 로고    scopus 로고
    • note
    • 2: C, 70.10; H, 9.15. Found: C, 69.94; H. 9.09.
  • 27
    • 67649866928 scopus 로고    scopus 로고
    • note
    • 13C NMR were identical to those of 2.
  • 29
    • 67649843779 scopus 로고    scopus 로고
    • note
    • 13C NMR were identical to those of 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.