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Kinetics and Catalysis
Volumn 52, Issue 4, 2011, Pages 525-528
Complex containing a Lewis acid and Brønsted acid for the catalytic reactions of aza-Michael addition
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EID: 80051628626     PISSN: 00231584     EISSN: None     Source Type: Journal    
DOI: 10.1134/S0023158411030207     Document Type: Article
Times cited : (5)
References (15)
  • 1
    • 0028003718 scopus 로고
    • Chemo- and diastereoselective reduction of β-enamino esters: A convenient synthesis of both cis- and trans-γ-amino alcohols and β-amino esters
    • DOI 10.1021/jo00097a039
    • G. Bartoli C. Cimarelli E. Marcantoni G. Palmieri M. Petrini 1994 J. Org. Chem. 59 5328 10.1021/jo00097a039 1:CAS:528:DyaK2cXmtlSgs70%3D (Pubitemid 24310991)
    • (1994) Journal of Organic Chemistry , vol.59 , Issue.18 , pp. 5328-5335
    • Bartoli, G.1    Cimarelli, C.2    Marcantoni, E.3    Palmieri, G.4    Petrini, M.5
  • 4
    • 40549143725 scopus 로고    scopus 로고
    • Efficient iron-catalyzed sakurai-michael addition of allyltrimethylsilane to chalcones
    • DOI 10.1080/00397910701860646, PII 791370418
    • L. Xu M. Yang H. Qiu G. Lai J. Jiang 2008 Synth. Commun. 38 1011 10.1080/00397910701860646 1:CAS:528:DC%2BD1cXjtVeksrs%3D (Pubitemid 351364141)
    • (2008) Synthetic Communications , vol.38 , Issue.7 , pp. 1011-1019
    • Xu, L.-W.1    Yang, M.-S.2    Qiu, H.-Y.3    Lai, G.-Q.4    Jiang, J.-X.5
  • 5
    • 39649104319 scopus 로고    scopus 로고
    • 10.1016/j.tetlet.2008.01.026 1:CAS:528:DC%2BD1cXis1CnsL8%3D
    • T. Miao L. Wang 2008 Tetrahedron Lett. 49 2173 10.1016/j.tetlet.2008.01. 026 1:CAS:528:DC%2BD1cXis1CnsL8%3D
    • (2008) Tetrahedron Lett. , vol.49 , pp. 2173
    • Miao, T.1    Wang, L.2
  • 6
    • 37249079113 scopus 로고    scopus 로고
    • Regio- and stereoselective one-pot synthesis of unknown oxazoline-fused pyridazines by 'Michael addition-pyridazine cyclization-oxazoline cyclization' cascade reactions of 4-chloro-1,2-diaza-1,3-butadienes with 3- dimethylaminopropenoates
    • DOI 10.1055/s-2007-990962
    • O. Attanasi G. Favi P. Filippone A. Golobic F. Perrulli B. Stanovnik J. Svete 2007 Synlett 19 2971 10.1055/s-2007-990962 (Pubitemid 350273148)
    • (2007) Synlett , Issue.19 , pp. 2971-2974
    • Attanasi, O.A.1    Favi, G.2    Filippone, P.3    Golobic, A.4    Perrulli, F.R.5    Stanovnik, B.6    Svete, J.7
  • 9
    • 38349049059 scopus 로고    scopus 로고
    • 10.1016/j.tetlet.2007.12.024 1:CAS:528:DC%2BD1cXosFamsw%3D%3D
    • B. Ni Q. Zhang A. Headley 2008 Tetrahedron Lett. 49 1249 10.1016/j.tetlet.2007.12.024 1:CAS:528:DC%2BD1cXosFamsw%3D%3D
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1249
    • Ni, B.1    Zhang, Q.2    Headley, A.3
  • 10
    • 38349073963 scopus 로고    scopus 로고
    • 10.1016/j.tetlet.2007.12.042 1:CAS:528:DC%2BD1cXosFamsg%3D%3D
    • A. Ziyaei-Halimehjani M. Saidi 2008 Tetrahedron Lett. 49 1244 10.1016/j.tetlet.2007.12.042 1:CAS:528:DC%2BD1cXosFamsg%3D%3D
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1244
    • Ziyaei-Halimehjani, A.1    Saidi, M.2
  • 14
    • 0001151145 scopus 로고
    • 10.1016/0021-9517(63)90102-7 1:CAS:528:DyaF2cXmsFSg
    • E.P. Parry 1963 J. Catal. 2 371 10.1016/0021-9517(63)90102-7 1:CAS:528:DyaF2cXmsFSg
    • (1963) J. Catal. , vol.2 , pp. 371
    • Parry, E.P.1
  • 15
    • 77950593698 scopus 로고    scopus 로고
    • 10.1016/j.apsusc.2010.02.049 1:CAS:528:DC%2BC3cXkvVaktb8%3D
    • B. Azambre L. Zenboury J.V. Weber P. Burg 2010 Appl. Surf. Sci. 256 4570 10.1016/j.apsusc.2010.02.049 1:CAS:528:DC%2BC3cXkvVaktb8%3D
    • (2010) Appl. Surf. Sci. , vol.256 , pp. 4570
    • Azambre, B.1    Zenboury, L.2    Weber, J.V.3    Burg, P.4

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.