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Volumn 11, Issue 18, 2000, Pages 3671-3674

Highly enantioselective borohydride reductions of 2-phenacylpyridine catalyzed by optically active β-ketoiminato cobalt(II) complexes

Author keywords

[No Author keywords available]

Indexed keywords

2 PHENACYLPYRIDINE; AMINE; COBALT COMPLEX; SEDAMINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034703162     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)00369-4     Document Type: Article
Times cited : (18)

References (16)
  • 1
    • 0007397107 scopus 로고    scopus 로고
    • In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999.
  • 2
    • 0007357704 scopus 로고    scopus 로고
    • Jacobsen, E. N. In Catalytic Asymmetric Synthesis; Ojima, I., Eds.; VCH: New York, 1993; pp. 159-202; Ito, Y. N.; Katsuki, T. Bull. Chem. Soc. Jpn. 1999, 72, 603.
  • 8
    • 0007397108 scopus 로고    scopus 로고
    • Ketoiminato ligands: Nagata, T.; Imagawa, K.; Yamada, T.; Mukaiyama, T. Bull. Chem. Soc. Jpn. 1995, 68, 1455. The cobalt(II) complex catalysts A, B and a series of complexes C (C, C', C-OEt, and C-O(c)Pen) were prepared from the optically active 1,2-diphenyl-1,2-ethylenediamine, 1,2-bis(3,5-dimethylphenyl)-1,2-ethylenediamine, and 1,2-bis(2,4,6-trimethylphenyl)-1,2-ethylenediamine, respectively
  • 11
    • 0007442212 scopus 로고    scopus 로고
    • note
  • 12
    • 0007359084 scopus 로고    scopus 로고
    • Manganese(III) chloride catalyst with the β-ketoimine C'-ligand and Jacobsen's cobalt(II) catalyst afforded the product with very low ee, although β-ketoiminato C' cobalt(II) catalyst and Jacobsen's manganese(III) chloride catalyst were very efficient on the reaction. Therefore, the combination of the center metal and the chiral ligand is essential for the highly enantioselective reduction of 2-phenacylpyridine.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.