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Volumn 10, Issue 20, 2008, Pages 4533-4536

Palladium-catalyzed direct arylation of nitro-substituted aromatics with aryl halides

Author keywords

[No Author keywords available]

Indexed keywords

HALOGEN; NITROBENZENE; NITROBENZENE DERIVATIVE; NITROGEN DERIVATIVE; PALLADIUM;

EID: 58149152745     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801839w     Document Type: Article
Times cited : (131)

References (70)
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    • For general reviews on direct arylation, see: a
    • For general reviews on direct arylation, see: (a) Alberico, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007, 107, 174.
    • (2007) Chem. Rev , vol.107 , pp. 174
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    • For recent examples using Pd(0), see: (a) Ackermann, L.; Vicente, R.; Born, R. Adv. Synth. Catal. 2008, 350, 741.
    • For recent examples using Pd(0), see: (a) Ackermann, L.; Vicente, R.; Born, R. Adv. Synth. Catal. 2008, 350, 741.
  • 20
    • 44949166937 scopus 로고    scopus 로고
    • For recent examples using Pd(II). see: (a) Beck, E. M.; Hatley, R.; Gaunt, M. J. Angew. Chem., Int. Ed. 2008, 47, 3004.
    • For recent examples using Pd(II). see: (a) Beck, E. M.; Hatley, R.; Gaunt, M. J. Angew. Chem., Int. Ed. 2008, 47, 3004.
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    • For recent examples using Rh(I). see: (e) Tsai, A. S.; Bergman, R. G.; Ellman, J. A. J. Am. Chem. Soc. 2008, 130, 6316.
    • For recent examples using Rh(I). see: (e) Tsai, A. S.; Bergman, R. G.; Ellman, J. A. J. Am. Chem. Soc. 2008, 130, 6316.
  • 34
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    • For reviews, see refs 3c and 3d. For recent examples, see: (a) Lane, B. S.: Sanies, D. Org. Lett. 2004, 6, 2897.
    • For reviews, see refs 3c and 3d. For recent examples, see: (a) Lane, B. S.: Sanies, D. Org. Lett. 2004, 6, 2897.
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    • Campeau, L.-C.; Schipper, D; Fagnou, K. J. Am. Chem. Soc. 2008, 130, 3266. See also ref 4e.
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    • For transformations of nitrobiphenyl into carbazole. see selected examples: c
    • For transformations of nitrobiphenyl into carbazole. see selected examples: (c) Sanz, R.; Escribano, J.; Pedrosa, M. R.; Aguado, R.; Arnáiz, F. J. Adv. Synth. Catal. 2007, 349, 713.
    • (2007) Adv. Synth. Catal , vol.349 , pp. 713
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  • 55
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    • For transformation of nitrobiphenyl to 2-hyrdoxybiphenyl, see selected examples: e
    • For transformation of nitrobiphenyl to 2-hyrdoxybiphenyl, see selected examples: (e) Boldt, P.; Bruhnke, D.; Gerson, F.; Scholz, M.; Jones, J. G.; Bär, F. Helv. Chim. Acta 1993, 76, 1739.
    • (1993) Helv. Chim. Acta , vol.76 , pp. 1739
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  • 56
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    • For transformation of nitrobiphenyl into 2-aminobiphenyl. see selected examples: f
    • For transformation of nitrobiphenyl into 2-aminobiphenyl. see selected examples: (f) Tafesh, A. M.; Weiguny, J. Chem. Rev. 1996, 96, 2035.
    • (1996) Chem. Rev , vol.96 , pp. 2035
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  • 62
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    • For transformation of nitrobiphenyl into 2-cyanobiphenyl, 2-chlorobiphenyl and 2-bromobiphenyl, see selected examples: l
    • For transformation of nitrobiphenyl into 2-cyanobiphenyl, 2-chlorobiphenyl and 2-bromobiphenyl, see selected examples: (l) Suzuki, N.; Azuma, T.; Kaneko, Y.; Izawa, Y.; Tomioka, H.; Nomoto, T. J. Chem. Soc., Perkin Trans. I 1987, 3, 645.
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    • Suzuki, N.1    Azuma, T.2    Kaneko, Y.3    Izawa, Y.4    Tomioka, H.5    Nomoto, T.6
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    • Incompete peak separation of the meta and para isomers in the crude GCMS analysis prevents a more precise measure of these two isomers separately. In most cases, the meta/para ratio was ∼2:1
    • Incompete peak separation of the meta and para isomers in the crude GCMS analysis prevents a more precise measure of these two isomers separately. In most cases, the meta/para ratio was ∼2:1.
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    • Ehrenfreund, J.; Lamberth, C.; Tobler, H.; Walter, H. WO pat. 2004, 058723.
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    • See the Supporting Information for details
    • See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.