메뉴 건너뛰기




Volumn 12, Issue 9, 2010, Pages 1599-1606

Solvent-free direct enantioselective aldol reaction using polystyrene-supported N-sulfonyl-(Ra)-binam-D-prolinamide as a catalyst

Author keywords

[No Author keywords available]

Indexed keywords


EID: 77956383171     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/c002967j     Document Type: Article
Times cited : (71)

References (93)
  • 1
    • 11844259698 scopus 로고    scopus 로고
    • R. Marhrwald, Ed.; Wiley-VCH, Weinheim, Vols 1 and 2
    • Modern Aldol Reactions, R. Marhrwald, Ed.; Wiley-VCH, Weinheim, 2004, Vols 1 and 2.
    • (2004) Modern Aldol Reactions
  • 2
    • 6044269452 scopus 로고    scopus 로고
    • For selected comprehensive books and selected reviews, see
    • For selected comprehensive books and selected reviews, see: P. I. Dalko L. Moisan Angew. Chem., Int. Ed. 2004 43 5138-5175.
    • (2004) Angew. Chem., Int. , vol.43 , pp. 5138-5175
    • Dalko, P.I.1    Moisan, L.2
  • 4
    • 28944440169 scopus 로고    scopus 로고
    • (thematic issue on Organocatalysis in Organic Synthesis, no. 2–3)
    • P. Kočovský, A. V. Malkov, Issue ed.; Tetrahedron, 2006, 62, 255 (thematic issue on Organocatalysis in Organic Synthesis, no. 2–3).
    • (2006) Tetrahedron , vol.62 , pp. 255
    • Kočovský, P.1    Malkov, A.V.2
  • 6
    • 55049138759 scopus 로고    scopus 로고
    • P. I. Dalko, Ed.; Wiley-VCH, Weinheim
    • Enantioselective Organocatalysis, P. I. Dalko, Ed.; Wiley-VCH, Weinheim, 2007.
    • (2007) Enantioselective Organocatalysis
  • 7
    • 38349142750 scopus 로고    scopus 로고
    • (Special Issue in Organocatalysis)
    • B. List Chem. Rev. 2007 107 5413.(Special Issue in Organocatalysis).
    • (2007) Chem. Rev. , vol.107 , pp. 5413
    • List, B.1
  • 25
    • 33748989516 scopus 로고    scopus 로고
    • For some recent examples of solvent free-asymmetric organocatalytic reactions, see
    • For some recent examples of solvent free-asymmetric organocatalytic reactions, see: A. Berkessel K. Roland J. M. Neudörfl Org. Lett. 2006 8 4195-4198.
    • (2006) Org. Lett. , vol.8 , pp. 4195-4198
    • Berkessel, A.1    Roland, K.2    Neudörfl, J.M.3
  • 45
    • 33745356347 scopus 로고    scopus 로고
    • (corrigendum: Tetrahedron: Asymmetry 2007, 18, 1031)
    • G. Guillena M. C. Hita C. Nájera Tetrahedron: Asymmetry 2006 17 1493-1497.(corrigendum: Tetrahedron: Asymmetry 2007, 18, 1031).
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1493-1497
    • Guillena, G.1    Hita, M.C.2    Nájera, C.3
  • 46
    • 33646494852 scopus 로고    scopus 로고
    • (corrigendum: Tetrahedron: Asymmetry 2007, 18, 1030)
    • G. Guillena M. C. Hita C. Nájera Tetrahedron: Asymmetry 2006 17 1027-1031.(corrigendum: Tetrahedron: Asymmetry 2007, 18, 1030).
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1027-1031
    • Guillena, G.1    Hita, M.C.2    Nájera, C.3
  • 51
    • 33846042523 scopus 로고    scopus 로고
    • (corrigendum: ARKIVOC 2007, i, 146–147)
    • G. Guillena M. C. Hita C. Nájera ARKIVOC 2007 iv 260-269. (corrigendum: ARKIVOC 2007, i, 146–147).
    • (2007) ARKIVOC , vol.4 , pp. 260-269
    • Guillena, G.1    Hita, M.C.2    Nájera, C.3
  • 73
    • 0026418434 scopus 로고
    • B. M. Trost Science 1991 254 1471-1477.
    • (1991) Science , vol.254 , pp. 1471-1477
    • Trost, B.M.1
  • 80
    • 85032776082 scopus 로고    scopus 로고
    • a)-1,1′-binaphthyl-2,2′-diamine was carried out in benzene as solvent, 75% yield of the sulfonyl derivative was achieved instead of the 65% yield obtained by performing the reaction in toluene
    • a)-1,1′-binaphthyl-2,2′-diamine was carried out in benzene as solvent, 75% yield of the sulfonyl derivative was achieved instead of the 65% yield obtained by performing the reaction in toluene.
  • 82
    • 85032771538 scopus 로고    scopus 로고
    • 1H NMR
    • 1H NMR.
  • 85
    • 33845728625 scopus 로고    scopus 로고
    • For further discussion and studies about the role of water in the aldol reaction see
    • For further discussion and studies about the role of water in the aldol reaction see: A. P. Brogan T. J. Dickerson K. D. Janda Angew. Chem., Int. Ed. 2006 45 8100-8102.
    • (2006) Angew. Chem., Int. , vol.45 , pp. 8100-8102
    • Brogan, A.P.1    Dickerson, T.J.2    Janda, K.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.