메뉴 건너뛰기




Volumn 42, Issue 1, 2003, Pages 112-114

The catalytic intermolecular orthoarylation of phenols

Author keywords

Arylation; Homogeneous catalysis; P ligands; Phenols; Rhodium

Indexed keywords

LIGANDS;

EID: 0347296197     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200390037     Document Type: Article
Times cited : (308)

References (22)
  • 3
    • 0025164652 scopus 로고
    • b) G. Bringmann, R. Walter, R. Weirich, Angew. Chem. 1990, 102, 1006; Angew. Chem. Int. Ed. Engl. 1990, 29, 977-991.
    • (1990) Angew. Chem. Int. Ed. Engl. , vol.29 , pp. 977-991
  • 12
    • 0030776292 scopus 로고    scopus 로고
    • a) T. Satoh, Y. Kawamura, M. Miura, M. Nomura, Angew. Chem. 1997, 109, 1820-1822; Angew. Chem. Int. Ed. Engl. 1997, 36, 1740-1742;
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1740-1742
  • 14
    • 0345971566 scopus 로고    scopus 로고
    • note
    • Miura and co-workers have demonstrated the 1-arylation of 2-naphthols. This pattern of reactivity presumably results from the high susceptibility of the 1-position to electrophilic attack rather than the formation of a highly strained four-membered palladacycle. See references [4].
  • 17
    • 0037167002 scopus 로고    scopus 로고
    • Very recently Yamaguchi and co-workers reported the gallium-catalyzed orthoalkynylation of phenols with haloalkynes: K. Kobayashi, M. Arisawa, M. Yamaguchi. J. Am. Chem. Soc. 2002, 124, 8528-8529.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 8528-8529
    • Kobayashi, K.1    Arisawa, M.2    Yamaguchi, M.3
  • 22
    • 0347862995 scopus 로고    scopus 로고
    • note
    • CCDC-192419 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB21EZ, UK; fax: (+44)1223-336-033; or deposit@ccdc.cam.ac.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.