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Volumn 62, Issue 7, 1997, Pages 2080-2092

Metalation vs Nucleophilic Addition in the Reactions of N-Phenethylimides with Organolithium Reagents. Ready Access to Isoquinoline Derivatives via N-Acyliminium Ions and Parham-Type Cyclizations

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EID: 0001157440     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo962155o     Document Type: Article
Times cited : (95)

References (35)
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    • For representative examples of π-nucleophiles, see: ref 7. For some recent examples, see: (a) Heaney, H.; Shuhaibar, K. F. Synlett 1995, 47. (b) Lee, Y. S.; Kang, D. W.; Lee, S. J.; Park, H. J. Org. Chem. 1995, 60, 7149. (c) Li, W. H.; Hanau, C. E.; Davignon, A.; Moeller, K. D. J. Org. Chem. 1995, 60, 8155. (d) Logers, M.; Overman, L. E.; Welmalker, G. S. J. Am. Chem. Soc. 1995, 117, 9139. (e) Marson, C. M.; Pink, J. H.; Smith, C. Tetrahedron Lett. 1995, 36, 8107. (f) Rigo, B.; Elghammarti, S.; Couturier, D. Tetrahedron Lett. 1996, 37, 485. (g) Yamada, H.; Aoyagi, S.; Kibayashi, C. J. Am. Chem. Soc. 1996, 118, 1054.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 9139
    • Logers, M.1    Overman, L.E.2    Welmalker, G.S.3
  • 18
    • 0028824251 scopus 로고
    • For representative examples of π-nucleophiles, see: ref 7. For some recent examples, see: (a) Heaney, H.; Shuhaibar, K. F. Synlett 1995, 47. (b) Lee, Y. S.; Kang, D. W.; Lee, S. J.; Park, H. J. Org. Chem. 1995, 60, 7149. (c) Li, W. H.; Hanau, C. E.; Davignon, A.; Moeller, K. D. J. Org. Chem. 1995, 60, 8155. (d) Logers, M.; Overman, L. E.; Welmalker, G. S. J. Am. Chem. Soc. 1995, 117, 9139. (e) Marson, C. M.; Pink, J. H.; Smith, C. Tetrahedron Lett. 1995, 36, 8107. (f) Rigo, B.; Elghammarti, S.; Couturier, D. Tetrahedron Lett. 1996, 37, 485. (g) Yamada, H.; Aoyagi, S.; Kibayashi, C. J. Am. Chem. Soc. 1996, 118, 1054.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 8107
    • Marson, C.M.1    Pink, J.H.2    Smith, C.3
  • 19
    • 0030070032 scopus 로고    scopus 로고
    • For representative examples of π-nucleophiles, see: ref 7. For some recent examples, see: (a) Heaney, H.; Shuhaibar, K. F. Synlett 1995, 47. (b) Lee, Y. S.; Kang, D. W.; Lee, S. J.; Park, H. J. Org. Chem. 1995, 60, 7149. (c) Li, W. H.; Hanau, C. E.; Davignon, A.; Moeller, K. D. J. Org. Chem. 1995, 60, 8155. (d) Logers, M.; Overman, L. E.; Welmalker, G. S. J. Am. Chem. Soc. 1995, 117, 9139. (e) Marson, C. M.; Pink, J. H.; Smith, C. Tetrahedron Lett. 1995, 36, 8107. (f) Rigo, B.; Elghammarti, S.; Couturier, D. Tetrahedron Lett. 1996, 37, 485. (g) Yamada, H.; Aoyagi, S.; Kibayashi, C. J. Am. Chem. Soc. 1996, 118, 1054.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 485
    • Rigo, B.1    Elghammarti, S.2    Couturier, D.3
  • 20
    • 0029962915 scopus 로고    scopus 로고
    • For representative examples of π-nucleophiles, see: ref 7. For some recent examples, see: (a) Heaney, H.; Shuhaibar, K. F. Synlett 1995, 47. (b) Lee, Y. S.; Kang, D. W.; Lee, S. J.; Park, H. J. Org. Chem. 1995, 60, 7149. (c) Li, W. H.; Hanau, C. E.; Davignon, A.; Moeller, K. D. J. Org. Chem. 1995, 60, 8155. (d) Logers, M.; Overman, L. E.; Welmalker, G. S. J. Am. Chem. Soc. 1995, 117, 9139. (e) Marson, C. M.; Pink, J. H.; Smith, C. Tetrahedron Lett. 1995, 36, 8107. (f) Rigo, B.; Elghammarti, S.; Couturier, D. Tetrahedron Lett. 1996, 37, 485. (g) Yamada, H.; Aoyagi, S.; Kibayashi, C. J. Am. Chem. Soc. 1996, 118, 1054.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 1054
    • Yamada, H.1    Aoyagi, S.2    Kibayashi, C.3


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