메뉴 건너뛰기




Volumn 2, Issue 2, 2011, Pages 312-315

Amine directed Pd(II)-catalyzed C-H bond functionalization under ambient conditions

Author keywords

[No Author keywords available]

Indexed keywords

AMBIENT CONDITIONS; ARYLATIONS; BUILDING BLOCKES; C-H BOND; CHEMICAL SYNTHESIS; COMPLEX ARCHITECTURES; FUNCTIONALIZATIONS; MOLECULAR FRAMEWORKS;

EID: 79952638920     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c0sc00367k     Document Type: Article
Times cited : (193)

References (51)
  • 1
    • 32644440329 scopus 로고    scopus 로고
    • For reviews of transition-metal-catalyzed C-H activation of arenes, see
    • For reviews of transition-metal-catalyzed C-H activation of arenes, see:A. R. Dick and M. S. Sanford, Tetrahedron, 2006, 62, 2439;
    • (2006) Tetrahedron , vol.62 , pp. 2439
    • Dick, A.R.1    Sanford, M.S.2
  • 12
    • 74949097467 scopus 로고    scopus 로고
    • For selected examples of C-H activation at room temperature, see
    • For selected examples of C-H activation at room temperature, see: B. Xiao, Y. Fu, J. Xu, T.J. Gong, J.J. Dai, J. Yi and L. Liu, J. Am. Chem. Soc., 2010, 132, 468;
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 468
    • Xiao, B.1    Fu, Y.2    Xu, J.3    Gong, T.J.4    Dai, J.J.5    Yi, J.6    Liu, L.7
  • 24
    • 52049102506 scopus 로고    scopus 로고
    • For Pd(II)-catalyzed C-H bond functionalizations on N-triflyl b-arylethylamines, see
    • For Pd(II)-catalyzed C-H bond functionalizations on N-triflyl b-arylethylamines, see J.-J. Li, T.-S. Mei and J.-Q. Yu, Angew. Chem., Int. Ed., 2008, 47, 6452-6455;
    • (2008) Angew. Chem., Int. Ed , vol.47 , pp. 6452-6455
    • Li, J.-J.1    Mei, T.-S.2    Yu, J.-Q.3
  • 28
    • 33845260504 scopus 로고    scopus 로고
    • For other examples of amine directed Pd-catalyzed C-H activation reactions, see
    • See also ref. 4, 5, 7a, 7c, and 10a
    • For other examples of amine directed Pd-catalyzed C-H activation reactions, see; A. Lazareva and O. Daugulis, Org. Lett., 2006, 8, 5211-5213. See also ref. 4, 5, 7a, 7c, and 10a.
    • (2006) Org. Lett , vol.8 , pp. 5211-5213
    • Lazareva, A.1    Daugulis, O.2
  • 29
    • 27144450136 scopus 로고    scopus 로고
    • For examples of Pd-catalyzed amination of aromatic C-H bonds see
    • For examples of Pd-catalyzed amination of aromatic C-H bonds see: W. C. P. Tsang, N. Zheng and S. L. Buchwald, J. Am. Chem. Soc., 2005, 127, 14560;
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 14560
    • Tsang, W.C.P.1    Zheng, N.2    Buchwald, S.L.3
  • 41
    • 74949120125 scopus 로고    scopus 로고
    • For examples of Pd-catalyzed C-H carbonylation
    • For examples of Pd-catalyzed C-H carbonylation, see R. Giri, J. K. Lam and J.-Q. Yu, J. Am. Chem. Soc., 2010, 132, 686-693;
    • (2010) Am. Chem. Soc , vol.132 , pp. 686-693
    • Giri, R.1    Lam, J.K.2    Yu, J.3
  • 42
    • 54849420705 scopus 로고    scopus 로고
    • See also ref. 2d
    • R. Giri and J.-Q. Yu, J. Am. Chem. Soc, 2008,130, 14082-14083. See also ref. 2d.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 14082-14083
    • Giri, R.1    Yu, J.-Q.2
  • 43
    • 79955584826 scopus 로고    scopus 로고
    • Isoquinolones can be accessed via applications of the Bischler-Napieralski reactions Strategic applications of named reactions in organic synthesis
    • Isoquinolones can be accessed via applications of the Bischler-Napieralski reactions. L. Kurti, B. Czako, in Strategic applications of named reactions in organic synthesis, Elsevier, 2005, pp. 62-63.
    • (2005) L. Kurti and B. Czako , pp. 62-63
    • Kurti, L.1    Czako, B.2
  • 44
    • 79955630205 scopus 로고    scopus 로고
    • Supporting Information For Stoichiometric Reactions From Palladacycle la
    • See supporting information for stoichiometric reactions from palladacycle 1a Pd.
  • 45
    • 58849130239 scopus 로고    scopus 로고
    • For Pd(II)-catalyzed ortho-directed C-H arylation with aryl boronic acids, see
    • For Pd(II)-catalyzed ortho-directed C-H arylation with aryl boronic acids, see: D.H.Wang, T.-S.Mei and J.Q. Yu, J. Am. Chem. Soc, 2008, 130, 17676-17677;
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 17676-17677
    • Wang, D.H.1    Mei, T.-S.2    Yu, J.Q.3
  • 47
    • 44949166937 scopus 로고    scopus 로고
    • For iterative metal-catalyzed C-H bond functionalizations in complex molecule synthesis, see
    • For iterative metal-catalyzed C-H bond functionalizations in complex molecule synthesis, see: E. M. Beck, R. Hatley and M. J. Gaunt, Angew. Chem., Int. Ed., 2008, 47, 3004.
    • (2008) Angew. Chem., Int. Ed , vol.47 , pp. 3004
    • Beck, E.M.1    Hatley, R.2    Gaunt, M.J.3
  • 48
    • 74849140130 scopus 로고    scopus 로고
    • The PMP group can be removed from isoquinolone 2a by oxidative cleavage using cerium ammonium nitrate in 75% yield. See SI for details
    • The PMP group can be removed from isoquinolone 2a by oxidative cleavage using cerium ammonium nitrate in 75% yield. See SI for details. M. Yamauchi, M. Masao, T. Miuara and M. Murakami, J. Am. Chem. Soc., 2010, 132, 54-55.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 54-55
    • Yamauchi, M.1    Masao, M.2    Miuara, T.3    Murakami, M.4
  • 49
    • 33845938814 scopus 로고    scopus 로고
    • For a discussion on the role of PivOH in Pd-catalyzed C-H bond functionalization, see
    • For a discussion on the role of PivOH in Pd-catalyzed C-H bond functionalization, see: M. LaFrance and K. J. Fagnou, J. Am. Chem. Soc., 2006, 128, 16496;
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 16496
    • Lafrance, M.1    Fagnou, K.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.