메뉴 건너뛰기




Volumn 10, Issue 16, 2008, Pages 3607-3609

Copper-mediated C-H bond arylation of arenes with arylboronic acids

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROCARBON; BORONIC ACID DERIVATIVE; COPPER; ORGANOMETALLIC COMPOUND;

EID: 54049087464     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol8013717     Document Type: Article
Times cited : (146)

References (45)
  • 1
    • 0036589259 scopus 로고    scopus 로고
    • An extensive review on aryl-aryl bond formation including Cu-mediated and Pd-catalyzed processes: Hassan, J, Sévignon, M, Gozzi, C, Schulz, E, Leraaire, M. Chem. Rev 2002, 102, 1359
    • An extensive review on aryl-aryl bond formation including Cu-mediated and Pd-catalyzed processes: Hassan, J.; Sévignon, M.; Gozzi, C.; Schulz, E.; Leraaire, M. Chem. Rev 2002, 102, 1359.
  • 2
    • 61349154023 scopus 로고    scopus 로고
    • Reviews on catalytic C-H bond functionalization: (a) Dyker, G., Ed. Handbook of C-H Transformations; Wiley-VCH: Weinheim, Germany, 2005.
    • Reviews on catalytic C-H bond functionalization: (a) Dyker, G., Ed. Handbook of C-H Transformations; Wiley-VCH: Weinheim, Germany, 2005.
  • 8
    • 33744801400 scopus 로고    scopus 로고
    • Recent progress in C-H bond functionlization catalyzed or mediated by Cu: (a) Li, C.-J.; Li, Z. Pure Appl. Chem. 2006, 78, 935.
    • Recent progress in C-H bond functionlization catalyzed or mediated by Cu: (a) Li, C.-J.; Li, Z. Pure Appl. Chem. 2006, 78, 935.
  • 24
    • 34249936878 scopus 로고    scopus 로고
    • Oxidative cross-coupling of two arenes catalyzed by Pd and mediated by Cu or Ag: (a) Stuart, D. R.; Fagnou, K. Science 2007, 316, 1172.
    • Oxidative cross-coupling of two arenes catalyzed by Pd and mediated by Cu or Ag: (a) Stuart, D. R.; Fagnou, K. Science 2007, 316, 1172.
  • 41
    • 61349111197 scopus 로고    scopus 로고
    • Under current conditions, efficient cross-coupling proceeds only with electron-rich benzene derivatives; simple substrates such as benzene or toluene are unreactive. A full scope of applicable arenes and arylboronic acids will be reported in due course
    • Under current conditions, efficient cross-coupling proceeds only with electron-rich benzene derivatives; simple substrates such as benzene or toluene are unreactive. A full scope of applicable arenes and arylboronic acids will be reported in due course.
  • 42
    • 34250029481 scopus 로고    scopus 로고
    • Selected recent examples: (a) Kuo, W.-J.; Chen, Y.-H.; Jeng, R.-J.; Chan, L.-H.; Lin, W.-P.; Yang, Z.-M. Tetrahedron 2007, 63, 7086.
    • Selected recent examples: (a) Kuo, W.-J.; Chen, Y.-H.; Jeng, R.-J.; Chan, L.-H.; Lin, W.-P.; Yang, Z.-M. Tetrahedron 2007, 63, 7086.
  • 43
    • 61349163449 scopus 로고    scopus 로고
    • Jpn. Kokai Tokkyo Koho JP2005232159;, 266809
    • (b) Yabe, M.; Fugono, M. Jpn. Kokai Tokkyo Koho JP2005232159; Chem. Abstr. 143, 266809.
    • Chem. Abstr , vol.143
    • Yabe, M.1    Fugono, M.2
  • 45
    • 11844268057 scopus 로고    scopus 로고
    • To completely rule out catalysis by ultra-low levels of Pd would be precocious. A cautionary report: Arvela, R. K.; Leadbeater, N. E.; Sangi, M. S.; Williams, V. A.; Granados, P.; Singer, R. D. J. Org. Chem. 2005, 70, 161.
    • To completely rule out catalysis by ultra-low levels of Pd would be precocious. A cautionary report: Arvela, R. K.; Leadbeater, N. E.; Sangi, M. S.; Williams, V. A.; Granados, P.; Singer, R. D. J. Org. Chem. 2005, 70, 161.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.