메뉴 건너뛰기




Volumn 48, Issue 33, 2009, Pages 6097-6100

Palladium(II)-catalyzed ortho alkylation of benzoic acids with alkyl halides

Author keywords

Alkylation; Benzoic acid; Benzolactones; C H activation

Indexed keywords

ALKYL HALIDES; ALKYLATION REACTIONS; BENZOIC ACID; BENZOLACTONES; C - H ACTIVATION; C-H BOND; CARBOXYLATE ANIONS; CATALYZED REACTIONS; INTRAMOLECULAR LACTONIZATION;

EID: 70349777759     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200902262     Document Type: Article
Times cited : (238)

References (64)
  • 1
    • 0000683502 scopus 로고
    • For the arylation of heterocycles see: a
    • For the arylation of heterocycles see: a) N. Nakamura, Y. Tajima, K. Sakai, Heterocycles 1982, 17, 235;
    • (1982) Heterocycles , vol.17 , pp. 235
    • Nakamura, N.1    Tajima, Y.2    Sakai, K.3
  • 10
    • 0031013608 scopus 로고    scopus 로고
    • 0-catalyzed arylation of arenes see: a D. D. Hennings, S. Iwasa, V. H. Rawal, J. Org. Chem. 1997, 62, 2;
    • 0-catalyzed arylation of arenes see: a) D. D. Hennings, S. Iwasa, V. H. Rawal, J. Org. Chem. 1997, 62, 2;
  • 13
    • 70349900132 scopus 로고    scopus 로고
    • 0-catalyzed intramolecular arylation of arenes see;
    • 0-catalyzed intramolecular arylation of arenes see;
  • 19
    • 0034620911 scopus 로고    scopus 로고
    • 2)-H bonds see: a) Y. Kametani, T. Satoh, M. Miura, M. Nomura, Tetrahedron Lett. 2000, 41. 2655;
    • 2)-H bonds see: a) Y. Kametani, T. Satoh, M. Miura, M. Nomura, Tetrahedron Lett. 2000, 41. 2655;
  • 24
    • 70349934869 scopus 로고    scopus 로고
    • 3)-H bonds see: a) G. Dyker, Angew. Chem. 1992, 104, 1079;
    • 3)-H bonds see: a) G. Dyker, Angew. Chem. 1992, 104, 1079;
  • 34
    • 35248816863 scopus 로고    scopus 로고
    • For recent reviews on the arylation of C, H bonds catalyzed by other transition metals see: a
    • For recent reviews on the arylation of C - H bonds catalyzed by other transition metals see: a) L. Ackermann, Top. Organomet. Chem. 2007, 24, 35;
    • (2007) Top. Organomet. Chem , vol.24 , pp. 35
    • Ackermann, L.1
  • 40
    • 0033961226 scopus 로고    scopus 로고
    • 2IX see: M. Xia, Z.-C. Chen, Synth. Commun. 2000, 30, 531.
    • 2IX see: M. Xia, Z.-C. Chen, Synth. Commun. 2000, 30, 531.
  • 47
    • 30744445455 scopus 로고    scopus 로고
    • For the Pd-catalyzed alkylation of C, H bonds with organometallic reagents see
    • For the Pd-catalyzed alkylation of C - H bonds with organometallic reagents see: X. Chen, J.-J. Li, X.-S. Hao, C. E. Goodhue, J.-Q. Yu, J. Am. Chem. Soc. 2006, 128. 78.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 78
    • Chen, X.1    Li, J.-J.2    Hao, X.-S.3    Goodhue, C.E.4    Yu, J.-Q.5
  • 48
    • 0141988949 scopus 로고    scopus 로고
    • For seminal work on Negishi cross-couplings with alkyl halides see
    • For seminal work on Negishi cross-couplings with alkyl halides see: J. Zhou, G. C. Fu, J. Am. Chem. Soc. 2003, 125, 12527.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 12527
    • Zhou, J.1    Fu, G.C.2
  • 51
    • 70349931785 scopus 로고    scopus 로고
    • 0-catalyzed alkylations using norbornene as the mediator see: a M. Catellani, F. Frignani, A. Rangoni, Angew. Chem. 1997, 109, 142;
    • 0-catalyzed alkylations using norbornene as the mediator see: a) M. Catellani, F. Frignani, A. Rangoni, Angew. Chem. 1997, 109, 142;
  • 54
    • 54849420705 scopus 로고    scopus 로고
    • and references therein. For detailed discussion and evidence for cation-promoted Pd insertion into C, H bonds see
    • For detailed discussion and evidence for cation-promoted Pd insertion into C - H bonds see: R. Giri, J.-Q. Yu, J. Am. Chem. Soc. 2008, 130, 14082, and references therein.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 14082
    • Giri, R.1    Yu, J.-Q.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.