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Volumn 11, Issue 3, 2009, Pages 583-586

Cascade palladium-catalyzed alkenyl aminocarbonylation/ Intramolecular aryl amidation: An annulative synthesis of 2-quinolones

Author keywords

[No Author keywords available]

Indexed keywords

BROMINATED HYDROCARBON; ISOQUINOLINE DERIVATIVE; PALLADIUM; QUINOLONE DERIVATIVE;

EID: 60749137679     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol802624e     Document Type: Article
Times cited : (97)

References (56)
  • 6
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    • Selected recent examples: (a) Nodwell, M.; Riffell, J. L.; Roberge, M.; Andersen, R. J. Org. Lett. 2008, 10, 1051.
    • Selected recent examples: (a) Nodwell, M.; Riffell, J. L.; Roberge, M.; Andersen, R. J. Org. Lett. 2008, 10, 1051.
  • 11
    • 48849087952 scopus 로고    scopus 로고
    • Selected examples: (a) Huang, J.; Chen, Y.; King, A. O.; Dilmeghani, M.; Larsen, R. D.; Faul, M. M. Org. Lett. 2008, 10, 2609.
    • Selected examples: (a) Huang, J.; Chen, Y.; King, A. O.; Dilmeghani, M.; Larsen, R. D.; Faul, M. M. Org. Lett. 2008, 10, 2609.
  • 19
    • 43449101554 scopus 로고    scopus 로고
    • Selected examples: (a) Viirre, R. D.; Evindar, G.; Batey, R. A. J. Org. Chem. 2008, 73, 3452.
    • Selected examples: (a) Viirre, R. D.; Evindar, G.; Batey, R. A. J. Org. Chem. 2008, 73, 3452.
  • 30
    • 52449113990 scopus 로고    scopus 로고
    • For examples of carbonylation used in combination with alternative palladium-catalyzed reactions, see: (a) Worlikar, S. A, Larock, R. C. J. Org. Chem. 2008, 73, 7175
    • For examples of carbonylation used in combination with alternative palladium-catalyzed reactions, see: (a) Worlikar, S. A.; Larock, R. C. J. Org. Chem. 2008, 73, 7175.
  • 43
    • 41149121790 scopus 로고    scopus 로고
    • Examples of palladium catalyzed aminocarbonylation: (a) Deagostino, A.; Larini, P.; Occhiato, E. G.; Pizzuto, L.; Prandi, C.; Venturello, P. J. Org. Chem. 2008, 73, 1941.
    • Examples of palladium catalyzed aminocarbonylation: (a) Deagostino, A.; Larini, P.; Occhiato, E. G.; Pizzuto, L.; Prandi, C.; Venturello, P. J. Org. Chem. 2008, 73, 1941.
  • 48
    • 62149147283 scopus 로고    scopus 로고
    • See the Supporting Information for further details
    • See the Supporting Information for further details.
  • 55
    • 62149126697 scopus 로고    scopus 로고
    • For example, reaction of styrene 5 with p-anisidine results in the formation of 58% of the expected isoquinolone, together with 17% of the corresponding indole.
    • For example, reaction of styrene 5 with p-anisidine results in the formation of 58% of the expected isoquinolone, together with 17% of the corresponding indole.
  • 56
    • 34548830666 scopus 로고    scopus 로고
    • For an example of the related alkenyl triflate-aryl halide substrates used in benzofuran synthesis, see
    • For an example of the related alkenyl triflate-aryl halide substrates used in benzofuran synthesis, see: Tadd, A. C.; Fielding, M. R.; Willis, M. C. Tetrahedron Lett. 2007, 48, 7578.
    • (2007) C. Tetrahedron Lett , vol.48 , pp. 7578
    • Tadd, A.C.1    Fielding, M.R.2    Willis, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.