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Volumn 2007, Issue 4, 2007, Pages 260-269

Highly selective direct aldol reaction organocatalyzed by (S)-BINAM-L-prolinamide and benzoic acid using α-chalcogen-substituted ketones as donors

Author keywords

Aldol reaction; Asymmetric synthesis; Diols; Enantioselectivity; Organocatalysis

Indexed keywords


EID: 33846042523     PISSN: 1551-7012     EISSN: 14246376     Source Type: Journal    
DOI: 10.3998/ark.5550190.0008.422     Document Type: Article
Times cited : (28)

References (71)
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    • For general reviews on the catalytic enantioselective aldol reaction, see: a
    • (a) For general reviews on the catalytic enantioselective aldol reaction, see: (a) Gröger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137.
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    • Gröger, H.1    Vogl, E.M.2    Shibasaki, M.3
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    • Jacobsen, E. N, Platz, A, Yamamoto, H. Eds, Springer: Heidelberg, Chap 29, pp
    • (c) Carreira E. M. In Comprehensive Asymmetric Catalysis, Jacobsen, E. N.; Platz, A.; Yamamoto, H. Eds.; Springer: Heidelberg, 1999, Vol. 3, Chap 29, pp 997.
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    • Vols, Marhrwald, R. Ed, Wiley-VCH: Weinheim
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    • (2004) Modern Aldol Reactions , vol.1-2
  • 21
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    • For the first proline catalyzed intramolecular reaction see: a
    • For the first proline catalyzed intramolecular reaction see: (a) List, B.; Lerner, R. A.; Barbas III, C. F. J. Am. Chem. Soc. 2000, 122, 2395.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 2395
    • List, B.1    Lerner, R.A.2    Barbas III, C.F.3
  • 67
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    • For the synthesis and structural properties of several BINAM prolinamides derived from acyclic amino acids see: Kowalczyk, B, Tarnowska, A, Weseliñski, L; Jurczak, J. Synlett 2005, 2372
    • (b) For the synthesis and structural properties of several BINAM prolinamides derived from acyclic amino acids see: Kowalczyk, B.; Tarnowska, A.; Weseliñski, L; Jurczak, J. Synlett 2005, 2372.
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    • For review about the use of α-hydroxyacetone derivatives in organic synthesis, see
    • For review about the use of α-hydroxyacetone derivatives in organic synthesis, see: Enders, D.; Voith, M.; Lenzen, A. Angew. Chem. Int. Ed. 2005, 44, 1304
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 1304
    • Enders, D.1    Voith, M.2    Lenzen, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.