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Volumn 67, Issue 17, 2011, Pages 3132-3139

A facile three-component [3+2]-cycloaddition/annulation domino protocol for the regio- and diastereoselective synthesis of novel penta- and hexacyclic cage systems, involving the generation of two heterocyclic rings and five contiguous stereocenters

Author keywords

Cage compounds; Dipolar cycloadditions; Domino reactions; Multicomponent reactions; Spiro compounds

Indexed keywords

CARBON; FUSED HETEROCYCLIC RINGS; IMINE; NITROGEN; SPIRO COMPOUND;

EID: 79953701317     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.02.058     Document Type: Article
Times cited : (31)

References (67)
  • 2
    • 2542509173 scopus 로고    scopus 로고
    • For selected reviews and monographs on multicomponent reactions, see: (a) A. Dömling, and I. Ugi Angew. Chem., Int. Ed. 39 2000 3168 3210
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3168-3210
    • Dömling, A.1    Ugi, I.2
  • 15
    • 70349769724 scopus 로고    scopus 로고
    • (c) Redox economy: N.Z. Burns, P.S. Baran, and R.W. Hoffmann Angew. Chem., Int. Ed. 48 2009 2854 2865 For a discussion on case-studies of the application of these principles to the total syntheses of complex molecules, see:
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 2854-2865
    • Burns, N.Z.1    Baran, P.S.2    Hoffmann, R.W.3
  • 19
    • 0034678033 scopus 로고    scopus 로고
    • For reviews of diversity-oriented synthesis, see (a) S.L. Schreiber Science 287 2000 1964 1969
    • (2000) Science , vol.287 , pp. 1964-1969
    • Schreiber, S.L.1
  • 26
    • 0004101860 scopus 로고
    • A. Padwa, Wiley New York, NY
    • For selected monographs on 1,3-dipolar cycloaddition reactions, see (a) A. Padwa, 1,3-Dipolar Cycloaddition Chemistry Vol. 1 and 2 1984 Wiley New York, NY
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.12
  • 29
    • 11544346529 scopus 로고    scopus 로고
    • For selected reviews on 1,3-dipolar cycloaddition reactions, see: (a) K.V. Gothelf, and K.A. Jørgensen Chem. Rev. 98 1998 863 910
    • (1998) Chem. Rev. , vol.98 , pp. 863-910
    • Gothelf, K.V.1    Jørgensen, K.A.2
  • 49
    • 79953677538 scopus 로고    scopus 로고
    • note
    • The 3,5-bis[(E)-arylmethylidene]tetrahydro-4(1H)-pyridinones (1) required for the present study were prepared from the reaction of 4-piperidone hydrochloride with aromatic aldehydes in the presence of HCl gas in acetic acid. See: Ref. 10a
  • 50
    • 0029078472 scopus 로고
    • For representative reviews and books on the use of microwave irradiation in synthetic organic chemistry, see: (a) S. Caddick Tetrahedron 38 1995 10403 10432
    • (1995) Tetrahedron , vol.38 , pp. 10403-10432
    • Caddick, S.1
  • 61
    • 43049126547 scopus 로고    scopus 로고
    • (l) Tetrahedron 62 2006 4623
    • (2006) Tetrahedron , vol.62 , pp. 4623
  • 62
    • 79953680787 scopus 로고    scopus 로고
    • For a review, See Ref, 15b
    • For a review, see Ref. 15b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.