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Volumn 6, Issue 11, 2004, Pages 1869-1871

Extending Pummerer reaction chemistry. Application to the oxidative cyclization of indole derivatives

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE; OXINDOLE; PHENYL GROUP; SPIRO COMPOUND;

EID: 2942594590     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0493406     Document Type: Article
Times cited : (48)

References (19)
  • 7
    • 0001272894 scopus 로고
    • Paquette, L. A., Ed.; John Wiley and Sons: New York
    • (b) de Lucchi, O.; Miotti, U.; Modena, G. In Organic Reactions; Paquette, L. A., Ed.; John Wiley and Sons: New York, 1991; Vol. 40, pp 157-405.
    • (1991) Organic Reactions , vol.40 , pp. 157-405
    • De Lucchi, O.1    Miotti, U.2    Modena, G.3
  • 9
    • 0011211458 scopus 로고    scopus 로고
    • Leading references to additive and vinylogous Pummerer reactions can be found in: (a) Padwa, A.; Kuethe, J. T. J. Org. Chem. 1998, 63, 4256-4268. (b) Shibata, N.; Fujimori, C.; Fujita, S.; Kita, Y. Chem. Pharm. Bull. 1996, 44, 892-894. (c) Marino, J. P.; Bogdan, S.; Kimura, K. J. Am. Chem. Soc. 1992, 114, 5566-5572.
    • (1998) J. Org. Chem. , vol.63 , pp. 4256-4268
    • Padwa, A.1    Kuethe, J.T.2
  • 10
    • 0030009170 scopus 로고    scopus 로고
    • Leading references to additive and vinylogous Pummerer reactions can be found in: (a) Padwa, A.; Kuethe, J. T. J. Org. Chem. 1998, 63, 4256-4268. (b) Shibata, N.; Fujimori, C.; Fujita, S.; Kita, Y. Chem. Pharm. Bull. 1996, 44, 892-894. (c) Marino, J. P.; Bogdan, S.; Kimura, K. J. Am. Chem. Soc. 1992, 114, 5566-5572.
    • (1996) Chem. Pharm. Bull. , vol.44 , pp. 892-894
    • Shibata, N.1    Fujimori, C.2    Fujita, S.3    Kita, Y.4
  • 11
    • 0000094637 scopus 로고
    • Leading references to additive and vinylogous Pummerer reactions can be found in: (a) Padwa, A.; Kuethe, J. T. J. Org. Chem. 1998, 63, 4256-4268. (b) Shibata, N.; Fujimori, C.; Fujita, S.; Kita, Y. Chem. Pharm. Bull. 1996, 44, 892-894. (c) Marino, J. P.; Bogdan, S.; Kimura, K. J. Am. Chem. Soc. 1992, 114, 5566-5572.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5566-5572
    • Marino, J.P.1    Bogdan, S.2    Kimura, K.3
  • 17
    • 0030742816 scopus 로고    scopus 로고
    • Similar selectivity for C(3) cyclization through an indole aryl-equatorial construct (cf. 22b) can be cited to rationalize observations in related systems. (a) Atarabashi, S.; Choi, J.-K.; Ha, D.-C.; Hart, D. J.; Kuzmich, D.; Lee, C.-S.; Ramesh, S.; Wu, S. C. J. Am. Chem. Soc. 1997, 119, 6226-6241. (b) Earley, W. G.; Oh, T.; Overman, L. E. Tetrahedron Lett. 1988, 29, 3785-3788.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6226-6241
    • Atarabashi, S.1    Choi, J.-K.2    Ha, D.-C.3    Hart, D.J.4    Kuzmich, D.5    Lee, C.-S.6    Ramesh, S.7    Wu, S.C.8
  • 18
    • 0023732619 scopus 로고
    • Similar selectivity for C(3) cyclization through an indole aryl-equatorial construct (cf. 22b) can be cited to rationalize observations in related systems. (a) Atarabashi, S.; Choi, J.-K.; Ha, D.-C.; Hart, D. J.; Kuzmich, D.; Lee, C.-S.; Ramesh, S.; Wu, S. C. J. Am. Chem. Soc. 1997, 119, 6226-6241. (b) Earley, W. G.; Oh, T.; Overman, L. E. Tetrahedron Lett. 1988, 29, 3785-3788.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 3785-3788
    • Earley, W.G.1    Oh, T.2    Overman, L.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.