Heckova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Heckova reakce" in Czech language version.

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acs.org

Carmen Drahl. In Names, History And Legacy. Chemical & Engineering News. 2010-05-17, s. 31–33. Dostupné online [cit. 2011-06-04].

Lorand Kiss; Tibor Kurtan; Sandor Antus; Henri Brunner. Further insight into the mechanism of Heck oxyarylation in the presence of chiral ligands. Arkivoc. 2003, s. GB–653J. Dostupné online. PMID 15957033.

Dennis Mc Cartney; Patrick J. Guiry. The asymmetric Heck and related reactions. Chemical Society Reviews. 2011, s. 5122–5150. PMID 21677934.
Yuzo Fujiwara; Ichiro Moritani; Sadao Danno; Ryuzo Asano; Shiichiro Teranishi. Aromatic substitution of olefins. VI. Arylation of olefins with palladium(II) acetate. Journal of the American Chemical Society. 1969, s. 7166–7169. PMID 27462934.
Michael Bradshaw; Jianli Zou; Lindsay Byrne; K. Swaminathan Iyer; Scott G. Stewart; Colin L. Raston. Pd(II) conjugated chitosan nanofibre mats for application in Heck cross-coupling reactions. Chemical Communications. 2011, s. 12 292 – 12 294. PMID 22011792.
Isahiro Hagiwara; Yoshitaka Sugawara; Takashi Hoshi; Toshio Suzuki. Sustainable Mizoroki–Heck reaction in water: remarkably high activity of Pd(OAc)₂ immobilized on reversed phase silica gel with the aid of an ionic liquid. Chemical Communications. 2005, s. 2942–2944. PMID 15957033.
Lorand Kiss; Tibor Kurtan; Sandor Antus; Henri Brunner. Further insight into the mechanism of Heck oxyarylation in the presence of chiral ligands. Arkivoc. 2003, s. GB–653J. Dostupné online. PMID 15957033.

LITTKE, A. F.; FU, G. C. Heck reactions of aryl chlorides catalyzed by palladium/tri-tert-butylphosphine: (E)-2-Methyl-3-phenylacrylic acid butyl ester and (E)-4-(2-phenylethenyl)benzonitrile. Org. Synth.. 2005, s. 63. Dostupné online.