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Volumn 121, Issue 7, 1999, Pages 1473-1478

Simple, highly active palladium catalysts for ketone and malonate arylation: Dissecting the importance of chelation and steric hindrance

Author keywords

[No Author keywords available]

Indexed keywords

MALONIC ACID; PALLADIUM;

EID: 0033599339     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja983378u     Document Type: Article
Times cited : (451)

References (51)
  • 14
    • 37049107355 scopus 로고
    • Malononitrile has been shown to react with aryl iodides with palladium catalysts to form the less readily hydrolyzed aryl malononitriles: Uno, M.; Seto, K.; Takahashi, S. J. Chem. Soc., Chem. Commun. 1984, 932-933.
    • (1984) J. Chem. Soc., Chem. Commun. , pp. 932-933
    • Uno, M.1    Seto, K.2    Takahashi, S.3
  • 27
    • 0344024538 scopus 로고    scopus 로고
    • 2 did not catalyze the ketone arylation and slowly gave biaryl product. One can understand the activity of this Pd/bisphosphine ratio in terms of the mechanistic data and results with the 1:1 Pd/monophosphine ratio described below
    • 2 did not catalyze the ketone arylation and slowly gave biaryl product. One can understand the activity of this Pd/bisphosphine ratio in terms of the mechanistic data and results with the 1:1 Pd/monophosphine ratio described below.
  • 28
    • 0344024536 scopus 로고    scopus 로고
    • This ligand is commercially available from Strem
    • This ligand is commercially available from Strem.
  • 32
    • 0344024534 scopus 로고    scopus 로고
    • To be submitted for publication
    • 2 in toluene and precipitation by addition of pentane. Mann, G.; Hartwig, J.F. To be submitted for publication.
    • Mann, G.1    Hartwig, J.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.