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Volumn 46, Issue 24, 2010, Pages 4291-4293

Palladium-catalyzed unsymmetrical aryl couplings in sequence leading to o-teraryls: Dramatic olefin effect on selectivity

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ARYL BORONIC ACID; ARYL BROMIDE; ARYL IODIDE; BORONIC ACID DERIVATIVE; BROMINE DERIVATIVE; CARBON; HYDROGEN; IODIDE; MALEIC ACID DIETHYL ESTER; PALLADIUM; UNCLASSIFIED DRUG;

EID: 77953306387     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c000526f     Document Type: Article
Times cited : (45)

References (42)
  • 24
    • 0042388114 scopus 로고    scopus 로고
    • Yield and selectivity decrease using a higher or lower amount of diethyl maleate. The latter was recovered together with ca. 20% of the corresponding E isomer (fumarate)
    • E. Motti A. Mignozzi M. Catellani J. Mol. Catal. A: Chem. 2003 204-205 115
    • (2003) J. Mol. Catal. A: Chem. , vol.204-205 , pp. 115
    • Motti, E.1    Mignozzi, A.2    Catellani, M.3
  • 37
    • 0034699894 scopus 로고    scopus 로고
    • Norbornene thus acts as catalyst. However, to favor its insertion into the arylpalladium bond of complex 7, norbornene must be present in sufficient concentration to counteract the Suzuki coupling11 at this stage. The best results were achieved using half the stoichiometric amount of norbornene
    • M. Catellani E. Motti S. Ghelli Chem. Commun. 2000 2003
    • (2000) Chem. Commun. , pp. 2003
    • Catellani, M.1    Motti, E.2    Ghelli, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.