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Volumn 2, Issue 2, 2011, Pages 349-352

In(III)-pybox complex catalyzed enantioselective Mukaiyama aldol reactions between polymeric or hydrated glyoxylates and enolsilanes derived from aryl ketones

Author keywords

[No Author keywords available]

Indexed keywords

ARYL KETONES; DIASTEREOSELECTIVITIES; ENANTIO; ENANTIOSELECTIVE; MILD REACTION CONDITIONS; MUKAIYAMA ALDOL REACTION; PYBOX COMPLEXES; SIMPLE OPERATION;

EID: 79955583920     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c0sc00454e     Document Type: Article
Times cited : (34)

References (89)
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    • Modern Aldol reactions. Vol. 2: Metal Catalysis, ed. R. Mahrwald, Wiley-VCH, Weinheim, 2004;
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    • E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer, Berlin
    • E. M. Carreira, in Comprehensive Asymmetric Catalysis, ed. E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer, Berlin, 1999, vol. 1, pp. 997-1065.
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    • Carreira, E.M.1
  • 20
    • 79955588194 scopus 로고    scopus 로고
    • 8-BINOL-based Brønsted acid catalyzed direct aldol reaction between aryl ketones and glyoxylates for which only moderate enantioselectivities were observed
    • while our manuscript under review, Blanchet and co-workers reported a H8-BINOL-based Brønsted acid catalyzed direct aldol reaction between aryl ketones and glyoxylates for which only moderate enantioselectivities were observed.
  • 32
    • 33644551895 scopus 로고    scopus 로고
    • Other Lewis-acid catalyzed Mukaiyama involving aryl enol silanes
    • Other Lewis-acid catalyzed Mukaiyama involving aryl enol silanes: J. Jankowska and J. Mlynarski, J. Org. Chem., 2006, 71, 1317-1321;
    • (2006) J. Org. Chem , vol.71 , pp. 1317-1321
    • Jankowska, J.1    Mlynarski, J.2
  • 66
    • 79955576303 scopus 로고    scopus 로고
    • 11% ee was obtained for enolsilane derived from unsubstituted acetophenone in Evans' case
    • 11% ee was obtained for enolsilane derived from unsubstituted acetophenone in Evans' case.
  • 87
    • 77957112412 scopus 로고    scopus 로고
    • DOI: 10.1016/j.tetlet.2010.06.066
    • J. F. Zhao, T. B. Tjan and T. P. Loh, Tetrahedron Lett., 2010, 51, 5649, DOI: 10.1016/j.tetlet.2010.06.066.
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    • Zhao, J.F.1    Tjan, T.B.2    Loh, T.P.3
  • 88
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    • For the effect of 4 A molecular sieves, see Table 7 of ESI†
    • For the effect of 4 A molecular sieves, see Table 7 of ESI†.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.