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Volumn , Issue 32, 2005, Pages 4039-4041

In situ formation of ligand and catalyst - Application in ruthenium-catalyzed enantioselective reduction of ketones

Author keywords

[No Author keywords available]

Indexed keywords

KETONE; LIGAND; RUTHENIUM DERIVATIVE;

EID: 23944519654     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b505516d     Document Type: Article
Times cited : (47)

References (33)
  • 28
    • 33645437276 scopus 로고    scopus 로고
    • note
    • 2 and (S)-1-amino-2-propanol, gave the corresponding secondary alcohol in 83% conversion and 67% ee (S-isomer).
  • 29
    • 0001704256 scopus 로고    scopus 로고
    • 2 we observed no product formation. However, Ru-complexes based on unprotected amino acids are reported to act as catalysts in the transfer hydrogenation of aryl alkyl ketones, see: (a) T. Ohta, S.-I. Nakahara, Y. Shigemura, K. Hattori and I. Furukawa, Chem. Lett., 1998, 491-492;
    • (1998) Chem. Lett. , pp. 491-492
    • Ohta, T.1    Nakahara, S.-I.2    Shigemura, Y.3    Hattori, K.4    Furukawa, I.5
  • 32
    • 33645424896 scopus 로고    scopus 로고
    • note
    • The proposed structure of catalyst 2 is displayed in Scheme 1. Attempts to isolate and analyze this complex have so far been unsuccessful.
  • 33
    • 33645448685 scopus 로고    scopus 로고
    • note
    • 2 gave 1-phenylethanol in merely 29% conversion with 96% ee (S-isomer, reaction time 1 h). See Scheme 1 for the result obtained with ligand 1b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.