메뉴 건너뛰기




Volumn 77, Issue 4, 2012, Pages 1891-1908

Total synthesis of (±)-rocaglamide via oxidation-initiated nazarov cyclization

Author keywords

[No Author keywords available]

Indexed keywords

ANTI-INFLAMMATORIES; NATURAL PRODUCTS; NAZAROV CYCLIZATION; PENTADIENYL; REACTION PATHWAYS; SYNTHETIC STRATEGIES; TOTAL SYNTHESIS;

EID: 84857206865     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo202366c     Document Type: Article
Times cited : (62)

References (125)
  • 38
    • 0001992172 scopus 로고
    • In; Paquette, L. A. John Wiley & Sons, Inc. New York
    • Habermas, K. L.; Denmark, S. E.; Jones, T. K. In Organic Reactions; Paquette, L. A., Ed.; John Wiley & Sons, Inc.: New York, 1994; Vol. 45, pp 1-158.
    • (1994) Organic Reactions , vol.45 , pp. 1-158
    • Habermas, K.L.1    Denmark, S.E.2    Jones, T.K.3
  • 46
    • 70349330341 scopus 로고    scopus 로고
    • Review on domino reactions of oxyallyl intermediates
    • Review on domino reactions of oxyallyl intermediates: Grant, T. N.; Rieder, C. J.; West, F. G. Chem. Commun. 2009, 5676
    • (2009) Chem. Commun. , pp. 5676
    • Grant, T.N.1    Rieder, C.J.2    West, F.G.3
  • 47
    • 70350470027 scopus 로고    scopus 로고
    • Interception of oxyallyl cation with halogen nucleophiles
    • Interception of oxyallyl cation with halogen nucleophiles: Marx, V. M.; Cameron, T. S.; Burnell, D. J. Tetrahedron Lett. 2009, 50, 7213-7216
    • (2009) Tetrahedron Lett. , vol.50 , pp. 7213-7216
    • Marx, V.M.1    Cameron, T.S.2    Burnell, D.J.3
  • 48
    • 76149084183 scopus 로고    scopus 로고
    • Interception of oxyallyl cation with carbon nucleophiles
    • Interception of oxyallyl cation with carbon nucleophiles: Marx, V. M.; Burnell, D. J. J. Am. Chem. Soc. 2010, 132, 1685-1689
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1685-1689
    • Marx, V.M.1    Burnell, D.J.2
  • 49
    • 78650891199 scopus 로고    scopus 로고
    • Oxyallyl cation-azide cycloaddition
    • Oxyallyl cation-azide cycloaddition: Scadang, O.; Ferguson, M. J.; West, F. G. Org. Lett. 2011, 13, 114-117
    • (2011) Org. Lett. , vol.13 , pp. 114-117
    • Scadang, O.1    Ferguson, M.J.2    West, F.G.3
  • 50
    • 79955013472 scopus 로고    scopus 로고
    • Wagner-Meerwein rearrangement of oxyallyl cation
    • Wagner-Meerwein rearrangement of oxyallyl cation: Huang, J.; Lebœuf, D.; Frontier, A. J. J. Am. Chem. Soc. 2011, 133, 6307-6317
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 6307-6317
    • Huang, J.1    Lebœuf, D.2    Frontier, A.J.3
  • 51
    • 79251479095 scopus 로고    scopus 로고
    • Interception of oxyallyl cation with nitrogen heterocycles
    • Interception of oxyallyl cation with nitrogen heterocycles: Marx, V. M.; LeFort, F. M.; Burnell, D. J. Adv. Synth. Catal. 2011, 353, 64-68
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 64-68
    • Marx, V.M.1    Lefort, F.M.2    Burnell, D.J.3
  • 58
    • 0034628238 scopus 로고    scopus 로고
    • See Supporting Information for experimental details
    • Nan, Y.; Miao, H.; Yang, Z. Org. Lett. 2000, 2, 297-299. See Supporting Information for experimental details
    • (2000) Org. Lett. , vol.2 , pp. 297-299
    • Nan, Y.1    Miao, H.2    Yang, Z.3
  • 111
    • 0001389728 scopus 로고
    • Synthesis of a vinyl allene oxide model of prostanoid formation in corals
    • Synthesis of a vinyl allene oxide model of prostanoid formation in corals: Corey, E. J.; Ritter, K.; Yus, M.; Najera, C. Tetrahedron Lett. 1987, 28, 3547-3550
    • (1987) Tetrahedron Lett. , vol.28 , pp. 3547-3550
    • Corey, E.J.1    Ritter, K.2    Yus, M.3    Najera, C.4
  • 112
    • 79851498246 scopus 로고    scopus 로고
    • A detailed investigation of this reaction was conducted in our laboratory, after the oxidation-initiated cyclization was employed in the synthesis of (±)-rocaglamide
    • A detailed investigation of this reaction was conducted in our laboratory, after the oxidation-initiated cyclization was employed in the synthesis of (±)-rocaglamide: Spencer, W. T.; Levin, M. L.; Frontier, A. J. Org. Lett. 2011, 13, 414-417
    • (2011) Org. Lett. , vol.13 , pp. 414-417
    • Spencer, W.T.1    Levin, M.L.2    Frontier, A.J.3
  • 115
    • 84857231047 scopus 로고
    • In; Landor, S. R. Landor, P. D. Academic Press Inc. New York
    • Landor, P. D. In The Chemistry of the Allenes; Landor, S. R.; Landor, P. D., Eds.; Academic Press Inc., New York, 1982; Vol. 1, pp 155-159.
    • (1982) The Chemistry of the Allenes , vol.1 , pp. 155-159
    • Landor, P.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.