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Volumn 78, Issue 3, 2009, Pages 635-644

Efficient syntheses of 1-azatricyclic ring systems from anthranylamide

Author keywords

Alkaloid; Ammonium Ylide; Cascade; Phenyliodonium Ylide; Rearrangement

Indexed keywords


EID: 65549153168     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-08-11544     Document Type: Article
Times cited : (5)

References (37)
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    • In this review examples are reported in which successful RCM reactions are performed utilizing substrates containing secondary and tertiary amines
    • Compain P. Adv. Synth. Catal. 349 (2007) 1829 In this review examples are reported in which successful RCM reactions are performed utilizing substrates containing secondary and tertiary amines
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 1829
    • Compain, P.1
  • 19
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    • For general reviews of the Stevens rearrangement, see:. Trost B.M., and Fleming I. (Eds), Wiley, Inc., Oxford
    • For general reviews of the Stevens rearrangement, see:. Markò I.E. In: Trost B.M., and Fleming I. (Eds). The Stevens and related rearrangements (1991), Wiley, Inc., Oxford 913
    • (1991) The Stevens and related rearrangements , pp. 913
    • Markò, I.E.1
  • 21
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    • For a recent review of the Stevens rearrangement of ammonium ylides, see
    • For a recent review of the Stevens rearrangement of ammonium ylides, see. Vanecko J.A., Wan H., and West F.G. Tetrahedron 62 (2006) 1043
    • (2006) Tetrahedron , vol.62 , pp. 1043
    • Vanecko, J.A.1    Wan, H.2    West, F.G.3
  • 23
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    • For some examples of [2,3]-rearrangement of allylic ammonium ylides, see:
    • For some examples of [2,3]-rearrangement of allylic ammonium ylides, see:. Clark J.S., and Middleton M.D. Lett. 4 (2002) 765
    • (2002) Lett. , vol.4 , pp. 765
    • Clark, J.S.1    Middleton, M.D.2
  • 30
    • 0001345526 scopus 로고
    • The copper-based catalysis has been demonstrated to be more effective:
    • The copper-based catalysis has been demonstrated to be more effective:. West F.G., Naidu B.N., and Tester R.W. Chem. 59 (1994) 6892
    • (1994) Chem. , vol.59 , pp. 6892
    • West, F.G.1    Naidu, B.N.2    Tester, R.W.3
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    • note
    • 1H 300 MHz NMR to be 15.9 Hz.
  • 32
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    • For the use of spirocyclic ammonium ylide rearrangements to prepare medium-sized azacycles, see:
    • For the use of spirocyclic ammonium ylide rearrangements to prepare medium-sized azacycles, see:. Wright D.L., Weekly R.M., Groff R., and McMills M. Tetrahedron Lett. 37 (1996) 2165
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2165
    • Wright, D.L.1    Weekly, R.M.2    Groff, R.3    McMills, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.