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Volumn 49, Issue 16, 2010, Pages 2922-2924

Asymmetric tandem wittig rearrangement/mannich reactions

Author keywords

Asymmetric synthesis; Imines; Mannich reaction; Rearrangements; Stereoselectivity

Indexed keywords

AMINO ALCOHOLS; AMINO ESTERS; ASYMMETRIC SYNTHESIS; HIGH SELECTIVITY; IMINES; MANNICH REACTIONS; REACTION SEQUENCES; STEREOSELECTIVE SYNTHESIS;

EID: 77950486025     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201000609     Document Type: Article
Times cited : (16)

References (37)
  • 1
    • 84892201764 scopus 로고    scopus 로고
    • Part 11 (Ed.: J.J. Li), Wiley, Hoboken
    • For general reviews on the Mannich reaction, see: a) P. Galatsis in Name Reactions for Homologations Part 11 (Ed.: J.J. Li), Wiley, Hoboken. 2009, p. 653;
    • (2009) Name Reactions for Homologations , pp. 653
    • Galatsis, P.1
  • 4
    • 9244234076 scopus 로고    scopus 로고
    • For reviews on the asymmetric synthesis of β-amino acids, see: a) J. A. Ma, Angew. Chem. 2003, 115, 4426;
    • (2003) Angew. Chem. , vol.115 , pp. 4426
    • Ma, J.A.1
  • 20
  • 27
    • 33750087308 scopus 로고    scopus 로고
    • b) For a "racemic" variant of this transformation, see: M. B. Bertrand, J. P. Wolfe, Org. Lett. 2006, 8, 4661.
    • (2006) Org. Lett. , vol.8 , pp. 4661
    • Bertrand, M.B.1    Wolfe, J.P.2
  • 28
    • 84862757200 scopus 로고    scopus 로고
    • The configuration of 4 was determined by X-ray crystallographic analysis. CCDC 763869 (4) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • The configuration of 4 was determined by X-ray crystallographic analysis. CCDC 763869 (4) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 29
    • 77950497409 scopus 로고    scopus 로고
    • Part II (Ed.: J. J. Li), Wiley, Hoboken
    • For reviews on the 1,2-Wittig rearrangement, see: a) J. P. Wolfe, N. J. Guthrie in Name Reactions for Homologations Part II (Ed.: J. J. Li), Wiley, Hoboken, 2009, p. 226;
    • (2009) Name Reactions for Homologations , pp. 226
    • Wolfe, J.P.1    Guthrie, N.J.2
  • 30
    • 33645791244 scopus 로고    scopus 로고
    • (Eds.: Z. Rappoport, I. Marek), Wiley, London
    • b) K. Tomooka in The Chemistry of Organolithium Compounds, Vol.2 (Eds.: Z. Rappoport, I. Marek), Wiley, London, 2004, p. 749;
    • (2004) The Chemistry of Organolithium Compounds , vol.2 , pp. 749
    • Tomooka, K.1
  • 37
    • 0030957591 scopus 로고    scopus 로고
    • and references therein
    • The syn-amino alcohol products could also be formed by reaction of the minor Z-imine stereoisomers through chair-like transition states. For further discussion, see: C. Gennari, A. Vulpetti, G. Pain, Tetrahedron 1997, 53, 5909, and references therein.
    • (1997) Tetrahedron , vol.53 , pp. 5909
    • Gennari, C.1    Vulpetti, A.2    Pain, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.