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Volumn 46, Issue 42, 2010, Pages 7936-7938

Formation of multi-stereogenic centers using a catalytic diastereoselective Henry reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; DIAMINE; NITROALKANE; NITROMETHANE; PHENYLPROPANOLAMINE; SULFONYLDIAMINE; UNCLASSIFIED DRUG;

EID: 77958487686     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0cc03022h     Document Type: Article
Times cited : (25)

References (49)
  • 1
    • 0003445429 scopus 로고    scopus 로고
    • E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer-Verlag, Berlin-Heidelberg, Ed.
    • M. Shibasaki and H. Gröger, in Comprehensive Asymmetric Catalysis I-III, ed., E. N. Jacobsen,,, A. Pfaltz, and, H. Yamamoto,, Springer-Verlag, Berlin-Heidelberg, 1999, ch. 29.3
    • (1999) Comprehensive Asymmetric Catalysis I-III
    • Shibasaki, M.1    Gröger, H.2
  • 30
    • 36849023965 scopus 로고    scopus 로고
    • Construction of three contiguous centers in the Henry reaction using chiral α-aminoaldehydes or α-oxyaldehydes:
    • T. Nitabaru N. Kumagai M. Shibasaki Tetrahedron Lett. 2008 49 272
    • (2008) Tetrahedron Lett. , vol.49 , pp. 272
    • Nitabaru, T.1    Kumagai, N.2    Shibasaki, M.3
  • 44
    • 72049100940 scopus 로고    scopus 로고
    • Examples for the construction of multi-stereogenic centers using diastereoselective Henry reaction:
    • R. Kowalczyk J. Skarzewski Tetrahedron: Asymmetry 2009 20 2467
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 2467
    • Kowalczyk, R.1    Skarzewski, J.2
  • 48
    • 0002451214 scopus 로고
    • Various allyl organometallic reagents and metal enolates react with chiral aldehydes within the similar trend. The reaction using (E)-crotyl boronates would be a representative example. See:
    • N. T. Anh O. Eisenstein Nouv. J. Chim. 1977 1 61
    • (1977) Nouv. J. Chim. , vol.1 , pp. 61
    • Anh, N.T.1    Eisenstein, O.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.