메뉴 건너뛰기




Volumn 132, Issue 40, 2010, Pages 14006-14008

Palladium-catalyzed intermolecular decarboxylative coupling of 2-phenylbenzoic acids with alkynes via C-H and C-C bond activation

Author keywords

[No Author keywords available]

Indexed keywords

C-C BOND ACTIVATION; GOOD YIELD; REACTION EFFICIENCY;

EID: 77957717041     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja106130r     Document Type: Article
Times cited : (262)

References (48)
  • 1
    • 77957706765 scopus 로고    scopus 로고
    • For reviews on the coupling via C-C bond cleavage, see
    • For reviews on the coupling via C-C bond cleavage, see
  • 10
    • 77957701176 scopus 로고    scopus 로고
    • For an excellent review, see
    • For an excellent review, see
  • 12
    • 77957709687 scopus 로고    scopus 로고
    • For leading references in decarboxylative Heck reactions, see
    • For leading references in decarboxylative Heck reactions, see
  • 14
    • 33746929476 scopus 로고    scopus 로고
    • For decarboxylative couplings of aromatic carboxylic acids, see
    • For decarboxylative couplings of aromatic carboxylic acids, see: Goossen, L. J., Deng, G., and Levy, L. M. Science 2006, 313, 662
    • (2006) Science , vol.313 , pp. 662
    • Goossen, L.J.1    Deng, G.2    Levy, L.M.3
  • 19
    • 77957700997 scopus 로고    scopus 로고
    • For recent examples using carboxylic acids as directing groups, see
    • For recent examples using carboxylic acids as directing groups, see
  • 33
    • 77957716888 scopus 로고    scopus 로고
    • For representative syntheses of phenanthrene dervatives using organohalides or organometallic reagents, see
    • For representative syntheses of phenanthrene dervatives using organohalides or organometallic reagents, see
  • 36
    • 77957718835 scopus 로고    scopus 로고
    • For more details, see Supporting Information
    • For more details, see Supporting Information.
  • 39
    • 77957698511 scopus 로고    scopus 로고
    • For mechanistically insightful examples, see
    • For mechanistically insightful examples, see
  • 46
    • 77957719165 scopus 로고    scopus 로고
    • 4 -3. Different levels of selectivity are reported for this kind of step: Unselective
    • 4 -3. Different levels of selectivity are reported for this kind of step: Unselective
  • 47
    • 0000913941 scopus 로고
    • Selectivity required for path a:, Org. Lett. 2010, 12, 2908 Selectivity required for path d: ref 10b., Org. Lett. 2010, 12, 1540 For Ni, see:, Org. Lett. 2010, 12, 3518 For Rh, see:, J. Am. Chem. Soc. 2010, 132, 9585
    • Larock, R. C., Doty, M. J., and Cacchi, S. J. Org. Chem. 1993, 58, 4579 Selectivity required for path a: Shi, Z., Cui, Y., and Jiao, N. Org. Lett. 2010, 12, 2908 Selectivity required for path d: ref 10b. Ding, S., Shi, Z., and Jiao, N. Org. Lett. 2010, 12, 1540 For Ni, see: Liu, C.-C., Parthasarathy, K., and Cheng, C.-H. Org. Lett. 2010, 12, 3518 For Rh, see: Rakshit, S., Patureau, F. W., and Glorius, F. J. Am. Chem. Soc. 2010, 132, 9585
    • (1993) J. Org. Chem. , vol.58 , pp. 4579
    • Larock, R.C.1    Doty, M.J.2    Cacchi, S.3    Shi, Z.4    Cui, Y.5    Jiao, N.6    Ding, S.7    Shi, Z.8    Jiao, N.9    Liu, C.-C.10    Parthasarathy, K.11    Cheng, C.-H.12    Rakshit, S.13    Patureau, F.W.14    Glorius, F.15


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.