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Volumn 127, Issue 19, 2005, Pages 6972-6973

High performance of Rh(Phebox) catalysts in asymmetric reductive aldol reaction: High anti-selectivity

Author keywords

[No Author keywords available]

Indexed keywords

2,6 BIS(2 OXAZOLINYL)PHENYL; ACRYLIC ACID DERIVATIVE; ACRYLIC ACID TERT BUTYL ESTER; BENZALDEHYDE; BENZENE DERIVATIVE; LIGAND; NITROGEN; PHOSPHINE; RHODIUM; SILANE; TOLUENE; TRANSITION ELEMENT; UNCLASSIFIED DRUG;

EID: 18744395482     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja050698m     Document Type: Article
Times cited : (138)

References (31)
  • 1
    • 0000699983 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Berlin. Chapter 29.1
    • For reviews of asymmetric aldol reactions: Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Berlin. 1999; Vol. III, Chapter 29.1, pp 997-1065.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3 , pp. 997-1065
    • Carreira, E.M.1
  • 2
    • 11844259698 scopus 로고    scopus 로고
    • Wiley-VCH: Weinheim, Germany, For anti-selective aldol, see Supporting Information, ref S2
    • Mahrwald, R., Ed. Modern Aldol Reactions; Wiley-VCH: Weinheim, Germany, 2004. For anti-selective aldol, see Supporting Information, ref S2.
    • (2004) Modern Aldol Reactions
    • Mahrwald, R.1
  • 26
    • 18744383830 scopus 로고    scopus 로고
    • note
    • 2O) catalyzed the reaction with S2 at 50°C to give 54% yield (anti:syn = 84:16, 85% ee for anti and 4% ee for syn).
  • 27
    • 18744382954 scopus 로고    scopus 로고
    • note
    • See the experimental data with methyl acrylate in the Supporting Information.
  • 30
    • 0000660169 scopus 로고    scopus 로고
    • Similar two-step RA with syn-selectivity was reported: Zhao, C.-X.; Bass, J.; Morken, J. P. Org. Lett. 2001, 3, 2839-2842.
    • (2001) Org. Lett. , vol.3 , pp. 2839-2842
    • Zhao, C.-X.1    Bass, J.2    Morken, J.P.3
  • 31
    • 33947468884 scopus 로고
    • Zimmerman, H. E.; Traxler, M. D. J. Am. Chem. Soc. 1957, 79, 1920-1923. The transition state was presumed by calculation of the hypothetical intermediates, rhodium-aldolate diastereomers; see, Supporting Information.
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 1920-1923
    • Zimmerman, H.E.1    Traxler, M.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.