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Volumn 46, Issue 7, 2007, Pages 1101-1104

A new approach for an organocatalytic multicomponent domino asymmetric reaction

Author keywords

Aldehydes; Asymmetry; Domino reactions; Multicomponent reactions; Organocatalysis

Indexed keywords

ALDEHYDES; CATALYST ACTIVITY; COVALENT BONDS; ENANTIOSELECTIVITY; REACTION KINETICS; SUBSTITUTION REACTIONS;

EID: 34248192461     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200604479     Document Type: Article
Times cited : (244)

References (64)
  • 1
    • 33646562191 scopus 로고    scopus 로고
    • For reviews on organocatalysis, see: a
    • For reviews on organocatalysis, see: a) M. Marigo, K. A. Jørgensen, Chem. Commun. 2006, 2001;
    • (2001) Chem. Commun , vol.2006
    • Marigo, M.1    Jørgensen, K.A.2
  • 7
  • 8
    • 34250740114 scopus 로고    scopus 로고
    • Acc. Chem. Res. 2004, 37, special issue on organocatalysis.
    • g) Acc. Chem. Res. 2004, 37, special issue on organocatalysis.
  • 9
    • 33744826542 scopus 로고    scopus 로고
    • For recent examples of enamine organocatalyzed reactions, see: a
    • For recent examples of enamine organocatalyzed reactions, see: a) Y. Chi, S. H. Gellman, J. Am. Chem. Soc. 2006, 128, 6804;
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 6804
    • Chi, Y.1    Gellman, S.H.2
  • 12
    • 20444441594 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3703;
    • (2005) Chem. Int. Ed , vol.44 , pp. 3703
    • Angew1
  • 14
  • 16
    • 22144459070 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4212;
    • (2005) Chem. Int. Ed , vol.44 , pp. 4212
    • Angew1
  • 18
    • 33845190114 scopus 로고    scopus 로고
    • For recent examples of organocatalyzed additions to α,β- unsaturated compounds, see: a
    • For recent examples of organocatalyzed additions to α,β- unsaturated compounds, see: a) S. Brandau, E. Maerten, K. A. Jørgensen, J. Am. Chem. Soc. 2006, 128, 14986;
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 14986
    • Brandau, S.1    Maerten, E.2    Jørgensen, K.A.3
  • 21
    • 33750440775 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 6853;
    • (2006) Chem. Int. Ed , vol.45 , pp. 6853
    • Angew1
  • 28
    • 33746286405 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 4193;
    • (2006) Chem. Int. Ed , vol.45 , pp. 4193
    • Angew1
  • 35
  • 40
    • 17144366282 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1602;
    • (2005) Chem. Int. Ed , vol.44 , pp. 1602
    • Angew1
  • 48
    • 8344250171 scopus 로고    scopus 로고
    • for pioneer work on asymmetric organocatalytic multicomponent three-bond-forming reaction, see: b
    • for pioneer work on asymmetric organocatalytic multicomponent three-bond-forming reaction, see: b) D. B. Ramachary, C. F. Barbas III, Chem. Eur. J. 2004, 10, 5323;
    • (2004) Chem. Eur. J , vol.10 , pp. 5323
    • Ramachary, D.B.1    Barbas III, C.F.2
  • 51
    • 1842851813 scopus 로고    scopus 로고
    • For reviews on the catalytic asymmetric construction of quaternary stereocenters, see: a
    • For reviews on the catalytic asymmetric construction of quaternary stereocenters, see: a) C. J. Douglas, L. E. Overman, Proc. Natl. Acad. Sci. USA 2004, 101, 5363;
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , pp. 5363
    • Douglas, C.J.1    Overman, L.E.2
  • 53
  • 55
  • 56
    • 34250778089 scopus 로고    scopus 로고
    • The reaction with the tBu ester was sluggish.
    • The reaction with the tBu ester was sluggish.
  • 62
    • 34250790964 scopus 로고    scopus 로고
    • 3N, Hünig's base) were tested but all gave inferior results.
    • 3N, Hünig's base) were tested but all gave inferior results.
  • 63
    • 84877935319 scopus 로고    scopus 로고
    • These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 627399 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via http://www.ccdc.cam.ac.uk/data_request/cif.
    • CCDC 627399 contains the supplementary crystallographic data for this paper
  • 64
    • 34250695722 scopus 로고    scopus 로고
    • Please note that the assignment of the face changes for the alkyl substituted α,β-unsaturated compounds
    • Please note that the assignment of the face changes for the alkyl substituted α,β-unsaturated compounds.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.