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Volumn , Issue 24, 2007, Pages 3877-3885

New paracyclophane phosphine for highly enantioselective ruthenium-catalyzed hydrogenation of prochiral ketones

Author keywords

Hydrogenation; Ketones; P,P ligands; Paracyclophane; Ruthenium

Indexed keywords

CATALYSIS; ENANTIOSELECTIVITY; HYDROGENATION; KETONES; LIGANDS; RUTHENIUM;

EID: 37549008696     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-990917     Document Type: Article
Times cited : (35)

References (27)
  • 5
    • 0003394736 scopus 로고
    • Brunner, H, Zettlmeier, W, Eds, Wiley-VCH: New York
    • Handbook of Enantioselective Catalysis, Vol. 2; Brunner, H.; Zettlmeier, W., Eds.; Wiley-VCH: New York, 1993.
    • (1993) Handbook of Enantioselective Catalysis , vol.2
  • 14
    • 33947300207 scopus 로고
    • For the preparation of the dibromide, see ref. 6, and for the preparation of the racemic dibromide, see
    • For the preparation of the dibromide, see ref. 6, and for the preparation of the racemic dibromide, see: Reich, H. J.; Cram, D. J. J. Am. Chem. Soc. 1969, 91, 3527.
    • (1969) J. Am. Chem. Soc , vol.91 , pp. 3527
    • Reich, H.J.1    Cram, D.J.2
  • 26
    • 37549031462 scopus 로고    scopus 로고
    • We used only the two diamines (R,R)-DPEN and (S,S)-DPEN; DPEN, 1,2-diphenylethylenediamine. Complex 6a was prepared by use of the (R,R)-amine, whereas the S,S, diamine was used for complex 6b
    • We used only the two diamines (R,R)-DPEN and (S,S)-DPEN; DPEN = 1,2-diphenylethylenediamine. Complex 6a was prepared by use of the (R,R)-amine, whereas the (S,S)- diamine was used for complex 6b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.