메뉴 건너뛰기




Volumn 14, Issue 4, 2008, Pages 1273-1281

Noncovalently supported heterogeneous chiral amine catalysts for asymmetric direct aldol and Michael addition reactions

Author keywords

Aldol reaction; Heterogeneous catalysis; Michael addition; Noncovalent immobilization; Organocatalysis

Indexed keywords

MICHAEL ADDITION; NONCOVALENCY; NONCOVALENT IMMOBILIZATION; ORGANOCATALYSIS;

EID: 38849124986     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200701129     Document Type: Article
Times cited : (112)

References (113)
  • 1
    • 11144263200 scopus 로고    scopus 로고
    • For selected reviews of organocatalysis, see: a
    • For selected reviews of organocatalysis, see: a) P. I. Dalko, L. Moisan, Angew. Chem. 2004, 116, 5248-5286;
    • (2004) Angew. Chem , vol.116 , pp. 5248-5286
    • Dalko, P.I.1    Moisan, L.2
  • 2
    • 6044269452 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 5138-5175;
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 5138-5175
  • 6
    • 0141619399 scopus 로고    scopus 로고
    • For comprehensive reviews, see: a
    • For comprehensive reviews, see: a) M. Benaglia, A. Puglisi, F. Cozzi, Chem. Rev. 2003, 103. 3401-3429;
    • (2003) Chem. Rev , vol.103 , pp. 3401-3429
    • Benaglia, M.1    Puglisi, A.2    Cozzi, F.3
  • 9
    • 38849167536 scopus 로고    scopus 로고
    • For a monograph on supported asymmetric catalysts, see: a Chiral Catalyst Immobilization and Recycling (Eds. : D. E. De Vos, I. F. Vankelecom, P. A. Jacobs), Wiley-VCH, Weinheim, 2000; for recent reviews on supported asymmetric catalysts, see:
    • For a monograph on supported asymmetric catalysts, see: a) Chiral Catalyst Immobilization and Recycling (Eds. : D. E. De Vos, I. F. Vankelecom, P. A. Jacobs), Wiley-VCH, Weinheim, 2000; for recent reviews on supported asymmetric catalysts, see:
  • 16
    • 33746840539 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 4732-4762.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 4732-4762
  • 37
    • 28844483203 scopus 로고    scopus 로고
    • for excellent new advances, see: For an excellent review on noncovalent immobilization, see: a
    • For an excellent review on noncovalent immobilization, see: a) J. Horn, F. Michalek, C. C. Tzschucke, W. Bannwarth, Top. Curr. Chem. 2004, 242, 43-75: for excellent new advances, see:
    • (2004) Top. Curr. Chem , vol.242 , pp. 43-75
    • Horn, J.1    Michalek, F.2    Tzschucke, C.C.3    Bannwarth, W.4
  • 54
    • 38849096526 scopus 로고    scopus 로고
    • For examples, see ref. [2c] and a S. Luo, X. Mi, L. Zhang, S. Liu, H. Xu, J.-P. Cheng, Angew. Chem. 2006, 118, 3165-3169;
    • For examples, see ref. [2c] and a) S. Luo, X. Mi, L. Zhang, S. Liu, H. Xu, J.-P. Cheng, Angew. Chem. 2006, 118, 3165-3169;
  • 55
    • 33746216402 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 3093-3097;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 3093-3097
  • 58
    • 33746834482 scopus 로고    scopus 로고
    • For a concept article, see
    • For a concept article, see: P. Barbaro, Chem. Eur. J. 2006, 12, 5666-5675.
    • (2006) Chem. Eur. J , vol.12 , pp. 5666-5675
    • Barbaro, P.1
  • 70
    • 24644443628 scopus 로고    scopus 로고
    • For excellent reviews, see: a
    • For excellent reviews, see: a) R. Haag, S. Roller, Top. Curr. Chem. 2004, 242, 1-42;
    • (2004) Top. Curr. Chem , vol.242 , pp. 1-42
    • Haag, R.1    Roller, S.2
  • 71
    • 0036810670 scopus 로고    scopus 로고
    • for recent examples on PS-supported nonchiral organocatalysts, see
    • b) C.A. McNamara, M. J. Dixon, M. Bradley, Chem. Rev. 2002, 102, 3275-3300; for recent examples on PS-supported nonchiral organocatalysts, see:
    • (2002) Chem. Rev , vol.102 , pp. 3275-3300
    • McNamara, C.A.1    Dixon, M.J.2    Bradley, M.3
  • 76
    • 38849095867 scopus 로고    scopus 로고
    • For reviews on direct aldol reactions, see: a. Modern Aldol Additions (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004;
    • For reviews on direct aldol reactions, see: a.) Modern Aldol Additions (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004;
  • 79
    • 0034678591 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1352-1374.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 1352-1374
  • 80
    • 34548540856 scopus 로고    scopus 로고
    • Strong solid acids, such as heteropoly acids, were applied in the present strategy and improved stereoselectivity was obtained; however, the reaction only worked under homogeneous conditions and lower activity or inert catalysis was observed under heterogeneous conditions; see
    • Strong solid acids, such as heteropoly acids, were applied in the present strategy and improved stereoselectivity was obtained; however, the reaction only worked under homogeneous conditions and lower activity or inert catalysis was observed under heterogeneous conditions; see: S. Luo, J. Li, H. Xu, L. Zhang, J.-P. Cheng, Org. Lett. 2007, 9, 3675-3678.
    • (2007) Org. Lett , vol.9 , pp. 3675-3678
    • Luo, S.1    Li, J.2    Xu, H.3    Zhang, L.4    Cheng, J.-P.5
  • 81
  • 105
    • 38849086773 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 42124215;
    • Angew. Chem. Int. Ed. 2005, 44, 42124215;
  • 110
    • 38849154577 scopus 로고    scopus 로고
    • Commercial sulfonated polystyrenes were systematically examined in this study; on the basis of the present results, it is highly possible that some commercial sulfonated polystyrenes may serve as good solid-acid supports in a manner similar to the acid supports used in this study by judicious selection of suitable loading amounts of the acid unit, proper cross-linking, and favorable particle size
    • Commercial sulfonated polystyrenes were systematically examined in this study; on the basis of the present results, it is highly possible that some commercial sulfonated polystyrenes may serve as good solid-acid supports in a manner similar to the acid supports used in this study by judicious selection of suitable loading amounts of the acid unit, proper cross-linking, and favorable particle size.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.