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Volumn 13, Issue 16, 2002, Pages 1789-1798

Asymmetric synthesis of aldol products derived from unsymmetrical ketones: Assignment of the absolute configuration of antibody aldol products

Author keywords

[No Author keywords available]

Indexed keywords

4 NITROBENZALDEHYDE; ALDEHYDE DERIVATIVE; ANTIBODY; CARBON; FRUCTOSE BISPHOSPHATE ALDOLASE; KETONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037183393     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00410-X     Document Type: Article
Times cited : (18)

References (30)
  • 1
    • 0000699983 scopus 로고    scopus 로고
    • Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Heidelberg, Chapters 29-1
    • For general reviews on the catalytic enantioselective aldol reaction: (a) Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Heidelberg, 1999; Vol. 3, Chapters 29-1; (b) Nelson, S. G. Tetrahedron: Asymmetry 1998, 9, 357; (c) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137; (d) Machajewski, T. D.; Wong, C.-H. Angew. Chem., Int. Ed. 2000, 39, 1352.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3
    • Carreira, E.M.1
  • 2
    • 0032512595 scopus 로고    scopus 로고
    • For general reviews on the catalytic enantioselective aldol reaction: (a) Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Heidelberg, 1999; Vol. 3, Chapters 29-1; (b) Nelson, S. G. Tetrahedron: Asymmetry 1998, 9, 357; (c) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137; (d) Machajewski, T. D.; Wong, C.-H. Angew. Chem., Int. Ed. 2000, 39, 1352.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 357
    • Nelson, S.G.1
  • 3
    • 0031849225 scopus 로고    scopus 로고
    • For general reviews on the catalytic enantioselective aldol reaction: (a) Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Heidelberg, 1999; Vol. 3, Chapters 29-1; (b) Nelson, S. G. Tetrahedron: Asymmetry 1998, 9, 357; (c) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137; (d) Machajewski, T. D.; Wong, C.-H. Angew. Chem., Int. Ed. 2000, 39, 1352.
    • (1998) Chem. Eur. J. , vol.4 , pp. 1137
    • Groger, H.1    Vogl, E.M.2    Shibasaki, M.3
  • 4
    • 0034678591 scopus 로고    scopus 로고
    • For general reviews on the catalytic enantioselective aldol reaction: (a) Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Heidelberg, 1999; Vol. 3, Chapters 29-1; (b) Nelson, S. G. Tetrahedron: Asymmetry 1998, 9, 357; (c) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137; (d) Machajewski, T. D.; Wong, C.-H. Angew. Chem., Int. Ed. 2000, 39, 1352.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 1352
    • Machajewski, T.D.1    Wong, C.-H.2
  • 9
    • 0000194961 scopus 로고
    • For a paper on the enantioselective synthesis of aldol products derived from methyl ketones and aliphatic aldehydes, see: Paterson, I.; Goodman, J. M.; Lister, M. A.; Schumann, C.; McClure, C. K.; Norcross, R. D. Tetrahedron 1990, 46, 4663. This methodology was not applied to methyl ketones including heteroatoms such as S or O in combination with the p-nitro substituted aromatic aldehydes.
    • (1990) Tetrahedron , vol.46 , pp. 4663
    • Paterson, I.1    Goodman, J.M.2    Lister, M.A.3    Schumann, C.4    McClure, C.K.5    Norcross, R.D.6
  • 19
    • 0005185922 scopus 로고    scopus 로고
    • The crystallographic data were deposited at the Cambridge Crystallographic Data Centre
    • The crystallographic data were deposited at the Cambridge Crystallographic Data Centre.
  • 28
    • 0005134389 scopus 로고    scopus 로고
    • The use of these reagents afforded a mixture of products arising from competitive processes such as dehydration and retroaldolization
    • The use of these reagents afforded a mixture of products arising from competitive processes such as dehydration and retroaldolization.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.