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Volumn 311, Issue 5761, 2006, Pages 642-644

Asymmetric hydrogenation of unfunctionalized, purely alkyl-substituted olefins

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; CHEMICAL BONDS; HYDROGENATION; INDIUM; SYNTHESIS (CHEMICAL);

EID: 31944450636     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1121977     Document Type: Article
Times cited : (278)

References (31)
  • 1
    • 0000701744 scopus 로고    scopus 로고
    • E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds. (Springer, Berlin), chap. 5.1
    • J. M. Brown, in Comprehensive Asymmetric Catalysis, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds. (Springer, Berlin, 1999), vol. I, chap. 5.1, pp. 121-182.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 121-182
    • Brown, J.M.1
  • 11
    • 31944452451 scopus 로고    scopus 로고
    • thesis, University of Basel
    • F. Menges, thesis, University of Basel (2004).
    • (2004)
    • Menges, F.1
  • 12
    • 31944444360 scopus 로고    scopus 로고
    • note
    • For related work of other research groups, see (13-18); for a review of catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes, see (19).
  • 20
    • 31944434261 scopus 로고    scopus 로고
    • thesis, University of Basel
    • S. Kaiser, thesis, University of Basel (2005).
    • (2005)
    • Kaiser, S.1
  • 21
    • 31944449225 scopus 로고    scopus 로고
    • note
    • See supporting material on Science Online.
  • 22
    • 31944449429 scopus 로고    scopus 로고
    • note
    • Catalysts were prepared as previously decribed; hydrogenations were carried out under standard conditions (5, 6).
  • 28
    • 31944441358 scopus 로고    scopus 로고
    • thesis. University of Basel
    • B. Wüstenberg, thesis. University of Basel (2003).
    • (2003)
    • Wüstenberg, B.1
  • 29
    • 31944451140 scopus 로고    scopus 로고
    • note
    • In the hydrogenation of the enantiomeric substrate (5)-16, >98% of (SRR)-17 was obtained with this ligand; this finding confirms that the stereoselectivity is controlled by the catalyst and that the influence of the stereogenic center in the substrate is negligible.
  • 30
    • 31944441125 scopus 로고    scopus 로고
    • note
    • The absolute configuration of the products has not yet been determined. The ee values are based on HPLC (product 8) and GC analysis (10) using chiral columns (21).
  • 31
    • 31944448455 scopus 로고    scopus 로고
    • note
    • Supported by the Swiss National Science Foundation, the Commission for Technology and Innovation (Switzerland), and DSM Nutritional Products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.