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Volumn 127, Issue 11, 2005, Pages 3790-3800

Chiral phosphine Lewis bases catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION ANALYSIS; CATALYSIS; HEATING; HYDROGEN BONDS; KETONES; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION KINETICS;

EID: 15744383666     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0447255     Document Type: Article
Times cited : (351)

References (105)
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    • (e) Imbriglio, J. E.; Vasbinder, M. M.; Miller, S. J. Org. Lett. 2003, 5, 3741-3743 and Miller, S. J. Acc. Chem. Res. 2004, 37, 601-610.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 601-610
    • Miller, S.J.1
  • 28
    • 2442700761 scopus 로고    scopus 로고
    • Schmalz, H.-G., Wirth, T., Eds.; Wiley-VCH: Weinheim, Germany
    • (u) Langer, P. Organic Synthesis Highlights V; Schmalz, H.-G., Wirth, T., Eds.; Wiley-VCH: Weinheim, Germany, 2003; pp 165-177.
    • (2003) Organic Synthesis Highlights V , pp. 165-177
    • Langer, P.1
  • 50
    • 4243830773 scopus 로고
    • (a) Baylis, A. B.; Hillman, M. E. D. Ger. Offen. 1972, 2, 155,113; Chem. Abstr. 1972, 77, 34174q; Hillman, M. E. D.; Baylis, A. B. U.S. Patent 1973, 3,743,669.
    • (1972) Chem. Abstr. , vol.77
    • Baylis, A.B.1    Hillman, M.E.D.2
  • 51
    • 15744382151 scopus 로고    scopus 로고
    • U.S. Patent 1973, 3,743,669
    • (a) Baylis, A. B.; Hillman, M. E. D. Ger. Offen. 1972, 2, 155,113; Chem. Abstr. 1972, 77, 34174q; Hillman, M. E. D.; Baylis, A. B. U.S. Patent 1973, 3,743,669.
    • Hillman, M.E.D.1    Baylis, A.B.2
  • 63
    • 0000077082 scopus 로고
    • For reports related to the aza-Baylis-Hillman reaction of methyl acrylate with N-sulfonated imines, please see: (h) Perlmutter, P.; Teo, C. C. Tetrahedron Lett. 1984, 25, 5951-5952.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 5951-5952
    • Perlmutter, P.1    Teo, C.C.2
  • 65
    • 0001266408 scopus 로고
    • For reports related to the aza-Baylis-Hillman reaction of MVK with N-sulfonated imine generated in situ, please see: (j) Bertenshow, S.; Kahn, M. Tetrahedron Lett. 1989, 30, 2731-2732.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2731-2732
    • Bertenshow, S.1    Kahn, M.2
  • 66
    • 0037023405 scopus 로고    scopus 로고
    • and references therein
    • (k) Balan, D.; Adolfsson, H. J. Org. Chem. 2002, 67, 2329-2334 and references therein.
    • (2002) J. Org. Chem. , vol.67 , pp. 2329-2334
    • Balan, D.1    Adolfsson, H.2
  • 69
    • 0038637120 scopus 로고    scopus 로고
    • The reaction mechanism for the Michael addition of methanol to α,β-unsaturated ketones has been disclosed recently: Stewart, I. C.; Bergman, R. G.; Toste, F. D. J. Am. Chem. Soc. 2003, 125, 8696-8697.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 8696-8697
    • Stewart, I.C.1    Bergman, R.G.2    Toste, F.D.3
  • 92
    • 15744381153 scopus 로고    scopus 로고
    • note
    • D.
  • 97


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.