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Volumn 13, Issue 2, 2007, Pages 574-581

Catalytic enantioselective domino oxa-michael/aldol condensations: Asymmetric synthesis of benzopyran derivatives

Author keywords

Asymmetric catalysis; Diphenylprolinol; Domino reactions; Heterocycles; Oxa michael reaction

Indexed keywords

CATALYSIS; CONDENSATION; DERIVATIVES;

EID: 33846250463     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200600572     Document Type: Article
Times cited : (212)

References (63)
  • 2
  • 4
    • 14844300078 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1366;
    • (2005) Chem. Int. Ed , vol.44 , pp. 1366
    • Angew1
  • 5
    • 84944049928 scopus 로고
    • Eds, A. R. Katrizky, C. W. Rees, Pergamon, Oxford
    • c) Comprehensive Heterocyclic Chemistry, Vol. 3 (Eds.: A. R. Katrizky, C. W. Rees), Pergamon, Oxford, 1984, pp. 737-883.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 737-883
  • 15
  • 19
    • 0348041984 scopus 로고    scopus 로고
    • and references therein; see also: G.-L. Zhao, J.-W. Huang, M. Shi, Org. Lett. 2003, 5, 4737.
    • and references therein; see also: G.-L. Zhao, J.-W. Huang, M. Shi, Org. Lett. 2003, 5, 4737.
  • 21
  • 24
  • 26
  • 27
    • 33846195287 scopus 로고    scopus 로고
    • For asymmetric organocatalytic reactions that employ the combination of enamine and iminium activation see: a N. Halland, P. S. Aburell, K. A. Jørgensen, Angew. Chem. 2004, 116, 1292;
    • For asymmetric organocatalytic reactions that employ the combination of enamine and iminium activation see: a) N. Halland, P. S. Aburell, K. A. Jørgensen, Angew. Chem. 2004, 116, 1292;
  • 28
    • 2342614099 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 1272;
    • (2004) Chem. Int. Ed , vol.4 , Issue.3 , pp. 1272
    • Angew1
  • 35
    • 33846185788 scopus 로고    scopus 로고
    • D. B. Ramachary, N. S. Chowdari, C. F. Barbas, III, Angew. Chem. 2003, 115, 4356;
    • h) D. B. Ramachary, N. S. Chowdari, C. F. Barbas, III, Angew. Chem. 2003, 115, 4356;
  • 36
  • 38
    • 23744473863 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4877.
    • (2005) Chem. Int. Ed , vol.44 , pp. 4877
    • Angew1
  • 39
    • 7044235263 scopus 로고    scopus 로고
    • For an excellent review on domino reactions see
    • For an excellent review on domino reactions see: L. F. Tietze, Chem. Rev. 1996, 96, 115.
    • (1996) Chem. Rev , vol.96 , pp. 115
    • Tietze, L.F.1
  • 40
    • 33846244084 scopus 로고    scopus 로고
    • We have also found that pyrrolidine catalyzes the racemic formation of chromene-3-carbaldehydes. G.-L. Zhao, H. Sundén, R. Rios, I. Ibrahem, A. Córdova, unpublished results.
    • We have also found that pyrrolidine catalyzes the racemic formation of chromene-3-carbaldehydes. G.-L. Zhao, H. Sundén, R. Rios, I. Ibrahem, A. Córdova, unpublished results.
  • 42
    • 14844283105 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1343;
    • (2005) Chem. Int. Ed , vol.44 , pp. 1343
    • Angew1
  • 45
    • 11144326714 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 6532;
    • (2004) Chem. Int. Ed , vol.43 , pp. 6532
    • Angew1
  • 48
  • 50
    • 33646573235 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 1952, and references therein.
    • Angew. Chem. Int. Ed. 2006, 45, 1952, and references therein.
  • 53
    • 0036263839 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 1650. Both enantiomers of α,aα-diphenylprolinol and α,α- bis(naphthalen-2-yl)prolinol are commercially available and can be TMS-protected in one step, see:
    • Angew. Chem. Int. Ed. 2002, 41, 1650. Both enantiomers of α,aα-diphenylprolinol and α,α- bis(naphthalen-2-yl)prolinol are commercially available and can be TMS-protected in one step, see:
  • 55
  • 57
    • 20444441594 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3703;
    • (2005) Chem. Int. Ed , vol.44 , pp. 3703
    • Angew1
  • 60
    • 22144459070 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4212;
    • (2005) Chem. Int. Ed , vol.44 , pp. 4212
    • Angew1


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