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Volumn 9, Issue 21, 2007, Pages 4223-4226

Applications of multicomponent reactions for the synthesis of diverse heterocyclic scaffolds

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; BIOLOGICAL PRODUCT; FUSED HETEROCYCLIC RINGS; ROELACTAMINE;

EID: 35548975293     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7018357     Document Type: Article
Times cited : (178)

References (54)
  • 4
    • 0037366605 scopus 로고    scopus 로고
    • For routes to privileged structures, see
    • For routes to privileged structures, see: Horton, D. A.; Bourne, G. T.; Smythe, M. L. Chem. Rev. 2003, 103, 893.
    • (2003) Chem. Rev , vol.103 , pp. 893
    • Horton, D.A.1    Bourne, G.T.2    Smythe, M.L.3
  • 30
    • 34250673184 scopus 로고    scopus 로고
    • For a recent example of a related application involving functional group pairing, see
    • For a recent example of a related application involving functional group pairing, see: Comer, E.; Rohan, E.; Deng, L.; Porco, J. A., Jr. Org. Lett. 2007, 9, 2123.
    • (2007) Org. Lett , vol.9 , pp. 2123
    • Comer, E.1    Rohan, E.2    Deng, L.3    Porco Jr., J.A.4
  • 34
    • 0034625424 scopus 로고    scopus 로고
    • For a review of additions to N-acyl iminium ions, see
    • For a review of additions to N-acyl iminium ions, see: Speckamp, W. N.; Moolenaar, M. J. Tetrahedron 2000, 56, 3817.
    • (2000) Tetrahedron , vol.56 , pp. 3817
    • Speckamp, W.N.1    Moolenaar, M.J.2
  • 35
    • 2442564600 scopus 로고    scopus 로고
    • For more recent examples see: a
    • For more recent examples see: (a) Fischer, C.; Camera, E. M. Org. Lett. 2004, 6, 1497.
    • (2004) Org. Lett , vol.6 , pp. 1497
    • Fischer, C.1    Camera, E.M.2
  • 41
    • 27944481736 scopus 로고    scopus 로고
    • For a related 4CR, see: Yin, Y.; Zhao, G.; Li, G.-L. Tetrahedron 2005, 61, 12042.
    • For a related 4CR, see: Yin, Y.; Zhao, G.; Li, G.-L. Tetrahedron 2005, 61, 12042.
  • 42
    • 33846906752 scopus 로고    scopus 로고
    • For a review of enantioselective additions to C=N bonds, see: Friestad, G. K.; Mathies, A. K. Tetrahedron 2007, 63, 2541.
    • For a review of enantioselective additions to C=N bonds, see: Friestad, G. K.; Mathies, A. K. Tetrahedron 2007, 63, 2541.
  • 45
    • 35548956264 scopus 로고    scopus 로고
    • The stereochemistry of 25 was established by correlating its NMR spectra with those of the corresponding aryl iodide, which was prepared similarly and the structure of which was established by X-ray analysis of its hydrochloride salt. The structure of 26 was also verified by X-ray analysis of its hydrochloride salt.
    • The stereochemistry of 25 was established by correlating its NMR spectra with those of the corresponding aryl iodide, which was prepared similarly and the structure of which was established by X-ray analysis of its hydrochloride salt. The structure of 26 was also verified by X-ray analysis of its hydrochloride salt.
  • 48
    • 0001528330 scopus 로고
    • For selected syntheses, see: a, Brossi, A, Ed, Academic Press: New York
    • For selected syntheses, see: (a) Gozler, B. The Alkaloids; Brossi, A, Ed.; Academic Press: New York, 1987; Vol. 31, pp 343.
    • (1987) The Alkaloids , vol.31 , pp. 343
    • Gozler, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.