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Volumn 15, Issue 18, 2013, Pages 4690-4693

Iron-catalyzed homocoupling of aryl halides and derivatives in the presence of alkyllithiums

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EID: 84884550802     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol401987s     Document Type: Article
Times cited : (45)

References (33)
  • 28
    • 19544373479 scopus 로고    scopus 로고
    • From the same starting 2-bomobenzyl bromide, 20 was also obtained by the magnesium way in three steps via the following: (i) homocoupling of an in situ formed benzyl Grignard; (ii) iodination of two aromatic bromide positions and iron catalyzed homocoupling of an in situ formed aryl magnesium (global yield: 19%)
    • From the same starting 2-bomobenzyl bromide, 20 was also obtained by the magnesium way in three steps via the following: (i) homocoupling of an in situ formed benzyl Grignard; (ii) iodination of two aromatic bromide positions and iron catalyzed homocoupling of an in situ formed aryl magnesium (global yield: 19%): Cahiez, G.; Chaboche, C.; Mahuteau-Betzer, F.; Ahr, M. Org. Lett. 2005, 7, 1943
    • (2005) Org. Lett. , vol.7 , pp. 1943
    • Cahiez, G.1    Chaboche, C.2    Mahuteau-Betzer, F.3    Ahr, M.4
  • 33
    • 84881110170 scopus 로고    scopus 로고
    • During the preparation of this manuscript the Pd-catalyzed cross-coupling of aryl halides with organolithium derivatives was published. This Palladium variant of the nickel system we described in ref 12 involves a strategy based on preformed aryllithiums, on halogen-lithium exchanges, and on direct metalations (as in the Fe-catalytic system descibed in this paper for the homocoupling)
    • During the preparation of this manuscript the Pd-catalyzed cross-coupling of aryl halides with organolithium derivatives was published. This Palladium variant of the nickel system we described in ref 12 involves a strategy based on preformed aryllithiums, on halogen-lithium exchanges, and on direct metalations (as in the Fe-catalytic system descibed in this paper for the homocoupling): Giannerini, M.; Fananas-Mastal, M.; Feringa Ben, L. Nat. Chem. 2013, 5, 667
    • (2013) Nat. Chem. , vol.5 , pp. 667
    • Giannerini, M.1    Fananas-Mastal, M.2    Feringa Ben, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.