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Volumn 54, Issue 43, 1998, Pages 13079-13086

Synthesis of biaryls via nickel-catalyzed cross-coupling reaction of arylboronic acids and aryl mesylates

Author keywords

[No Author keywords available]

Indexed keywords

BORONIC ACID DERIVATIVE; MESYLIC ACID DERIVATIVE; NICKEL; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 0032558595     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00809-6     Document Type: Article
Times cited : (80)

References (19)
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    • Miyaura, N.1
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    • (1996) Tetrahedron Lett. , vol.37 , pp. 2993
    • Saito, S.1    Sakai, M.2    Miyaura, N.3
  • 6
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    • 4 Saito, S.; Sakai, M.; Miyaura, N. Tetrahedron Lett. 1996, 37, 2993. Saito, S.; Oh-tani, S.; Miyaura, N. J. Org. Chem. 1997, 62, 8024. Indolese, A. F. Tetrahedron Lett. 1997, 38, 3513.
    • (1997) J. Org. Chem. , vol.62 , pp. 8024
    • Saito, S.1    Oh-tani, S.2    Miyaura, N.3
  • 7
    • 0030921405 scopus 로고    scopus 로고
    • 4 Saito, S.; Sakai, M.; Miyaura, N. Tetrahedron Lett. 1996, 37, 2993. Saito, S.; Oh-tani, S.; Miyaura, N. J. Org. Chem. 1997, 62, 8024. Indolese, A. F. Tetrahedron Lett. 1997, 38, 3513.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 3513
    • Indolese, A.F.1
  • 8
    • 0001322607 scopus 로고
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    • Kong, K.-C.1    Cheng, C.-H.2
  • 11
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    • 7 Stille, J. K. Angew. Chem. Int. Ed. Engl. 1986, 25, 508. Farina, V.; Roth, G. P. Advances in Metal-Organic Chemistry, Liebeskind, L. S. Ed.: JAI Press: London, 1996; Vol. 5, pp 1-53.
    • (1986) Angew. Chem. Int. Ed. Engl. , vol.25 , pp. 508
    • Stille, J.K.1
  • 12
    • 0002079003 scopus 로고    scopus 로고
    • Liebeskind, L. S. Ed.: JAI Press: London
    • 7 Stille, J. K. Angew. Chem. Int. Ed. Engl. 1986, 25, 508. Farina, V.; Roth, G. P. Advances in Metal-Organic Chemistry, Liebeskind, L. S. Ed.: JAI Press: London, 1996; Vol. 5, pp 1-53.
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  • 14
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    • note
    • 2O did not further accelerate the coupling.
  • 15
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    • 10 Kuvilla, H. G.; Nahabedian, K. V. J. Am. Chem. Soc. 1961, 83, 2159, 2164, and 2167. Kuvila, H. G.; Reuwer, J. F.; Mangravite, J. A. J. Am. Chem. Soc. 1964, 86, 2666.
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    • Kuvilla, H.G.1    Nahabedian, K.V.2
  • 18
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    • Academic: New York
    • 3. The highly dry boronic acids containing the boroxine more than 90% were used for the reaction. The preparation of arylboronic acids, see; Onak, T. Organoborane Chemistry; Academic: New York, 1975. Nesmeyanov, A. N.; Sokolik, R. A. Methods of Elemento-Organic Chemistry; North-Holland: Amsterdam, 1967; Vol. 1.
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    • Onak, T.1
  • 19
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    • North-Holland: Amsterdam
    • 3. The highly dry boronic acids containing the boroxine more than 90% were used for the reaction. The preparation of arylboronic acids, see; Onak, T. Organoborane Chemistry; Academic: New York, 1975. Nesmeyanov, A. N.; Sokolik, R. A. Methods of Elemento-Organic Chemistry; North-Holland: Amsterdam, 1967; Vol. 1.
    • (1967) Methods of Elemento-Organic Chemistry , vol.1
    • Nesmeyanov, A.N.1    Sokolik, R.A.2


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