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Volumn 73, Issue 8, 2008, Pages 3040-3046

Free radical-mediated aryl amination: Convergent two- and three-component couplings to chiral 2,3-disubstituted indolines

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CYCLIZATION; PHASE TRANSITIONS; REACTION KINETICS;

EID: 42149122127     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702523u     Document Type: Article
Times cited : (38)

References (97)
  • 18
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    • Selected total syntheses: Woodward, R. B.; Cava, M. P.; Ollis, W. D.; Hunger, A.; Daeniker, H. U.; Schenker, K. J. Am. Chem. Soc. 1954, 76, 4749.
    • Selected total syntheses: Woodward, R. B.; Cava, M. P.; Ollis, W. D.; Hunger, A.; Daeniker, H. U.; Schenker, K. J. Am. Chem. Soc. 1954, 76, 4749.
  • 28
    • 0000438986 scopus 로고    scopus 로고
    • Asymmetric Heck cyclizations (generally limited to cyclic or 1,1-disubstituted olefins, although exceptions exist): (a) Sato, Y.; Sodeoka, M.; Shibasaki, M. J. Org. Chem. 1989, 54, 4738.
    • Asymmetric Heck cyclizations (generally limited to cyclic or 1,1-disubstituted olefins, although exceptions exist): (a) Sato, Y.; Sodeoka, M.; Shibasaki, M. J. Org. Chem. 1989, 54, 4738.
  • 35
    • 0030760535 scopus 로고    scopus 로고
    • For enantioselective functionalization of indoles (hydrogenation), see: (a) Wagaw, S.; Rennels, R. A.; Buchwald, S. L. J. Am. Chem. Soc. 1997, 119, 8451.
    • For enantioselective functionalization of indoles (hydrogenation), see: (a) Wagaw, S.; Rennels, R. A.; Buchwald, S. L. J. Am. Chem. Soc. 1997, 119, 8451.
  • 37
    • 0036009480 scopus 로고    scopus 로고
    • Additional indoline annulations: Deboves, H. J. C.; Hunter, C.; Jackson, R. F. W. J. Chem. Soc. Perkin Trans. 1 2002, 733.
    • Additional indoline annulations: Deboves, H. J. C.; Hunter, C.; Jackson, R. F. W. J. Chem. Soc. Perkin Trans. 1 2002, 733.
  • 46
    • 0035902407 scopus 로고    scopus 로고
    • Additional leading references: O'Donnell, M. J.; Delgado, F.; Dominguez, E.; de Blas, J.; Scott, W. L. Tetrahedron: Asymmetry 2001, 12, 821.
    • Additional leading references: O'Donnell, M. J.; Delgado, F.; Dominguez, E.; de Blas, J.; Scott, W. L. Tetrahedron: Asymmetry 2001, 12, 821.
  • 62
    • 33847030354 scopus 로고    scopus 로고
    • Additional selected references: Ma, B.; Parkinson. J. L.; Castle, S. L. Tetrahedron Lett. 2007, 48, 2083.
    • Additional selected references: Ma, B.; Parkinson. J. L.; Castle, S. L. Tetrahedron Lett. 2007, 48, 2083.
  • 75
    • 0035948184 scopus 로고    scopus 로고
    • Reviews of carbon radical additions to azomethine derivatives
    • Reviews of carbon radical additions to azomethine derivatives: Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (2001) Tetrahedron , vol.57 , pp. 5461
    • Friestad, G.K.1
  • 80
    • 0004166052 scopus 로고
    • For leading references to epimerization of unactivated C-H bonds, see:, Sinnott, M, Ed, Academic Press: San Diego
    • For leading references to epimerization of unactivated C-H bonds, see: Tanner, M. E.; Kenyon, G. L. In Comprehensive Biological Catalysis; Sinnott, M., Ed.; Academic Press: San Diego, 1988; Vol. 2.
    • (1988) Comprehensive Biological Catalysis , vol.2
    • Tanner, M.E.1    Kenyon, G.L.2
  • 83
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    • Polar effects in radical reactions: Della, E. W.; Kostakis, C.; Smith, P. A. Org. Lett. 1999, 1, 363.
    • Polar effects in radical reactions: Della, E. W.; Kostakis, C.; Smith, P. A. Org. Lett. 1999, 1, 363.
  • 88
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    • Preliminary screening of cinchonidine-derived phase-transfer catalysts (only) failed to produce products with significant enantioenrichment. See the following leading references for enantioselective Schiff base conjugate additions: Almasi, D.; Alonso, D. A.; Najera, C. Tetrahedron: Asymmetry 2007, 18, 299.
    • Preliminary screening of cinchonidine-derived phase-transfer catalysts (only) failed to produce products with significant enantioenrichment. See the following leading references for enantioselective Schiff base conjugate additions: Almasi, D.; Alonso, D. A.; Najera, C. Tetrahedron: Asymmetry 2007, 18, 299.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.