赫克反应 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "赫克反应" in Chinese language version.

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11doi.org

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Lorand Kiss, Tibor Kurtan, Sandor Antus, Henri Brunner. Further insight into the mechanism of Heck oxyarylation in the presence of chiral ligands (free fulltext). Arkivoc. 2003: GB–653J [2010-10-07]. （原始内容存档于2006-05-18）.
Mitsuru Kitamura, Daisuke Kudo, and Koichi Narasaka. Palladium(0)-catalyzed synthesis of pyridines from β-acetoxy-γ,δ-unsaturated ketone oximes (free fulltext). Arkivoc. 2005: JC–1563E.

doi.org

Heck, R. F.; Nolley, Jr., J. P. Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides. J. Org. Chem. 1972, 37(14): 2320–2322. doi:10.1021/jo00979a024.
Mizoroki, T.; Mori, K.; Ozaki, A. Arylation of Olefin with Aryl Iodide Catalyzed by Palladium. Bull. Chem. Soc. Jap. 1971, 44: 581. doi:10.1246/bcsj.44.581.
Heck, R. F. Palladium-catalyzed vinylation of organic halides. Org. React. 1982, 27: 345–390. ISBN 978-0471264187. doi:10.1002/0471264180.or027.02.
A. de Meijere, F. E. Meyer, Jr.;. Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb. Angew. Chem. Int. Ed. Engl. 1994, 33: 2379–2411. doi:10.1002/anie.199423791.
Beletskaya, I. P.; Cheprakov, A. V. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chem. Rev. 2000, 100: 3009–3066. doi:10.1021/cr9903048.
Motitani, Ichiro; Fujiwara, Yuzo. Aromatic substitution of styrene-palladium chloride complex. Tetrahedron Letters. 1967, 8: 1119. doi:10.1016/S0040-4039(00)90648-8.
Heck, Richard F. Mechanism of arylation and carbomethoxylation of olefins with organopalladium compounds. Journal of the American Chemical Society. 1969, 91: 6707. doi:10.1021/ja01052a029.
Dieck, H. A.; Heck, R. F. Organophosphinepalladium complexes as catalysts for vinylic hydrogen substitution reactions. Journal of the American Chemical Society. 1974, 96: 1133. doi:10.1021/ja00811a029.
Ozawa, F.; Kubo, A.; Hayashi, T. Generation of Tertiary Phosphine-Coordinated Pd(0) Species from Pd(OAc)2 in the Catalytic Heck Reaction. Chemistry Lett. 1992: 2177–2180. doi:10.1246/cl.1992.2177.
De Vries, Johannes G. The Heck reaction in the production of fine chemicals. Canadian Journal of Chemistry. 2001, 79: 1086. doi:10.1139/cjc-79-5-6-1086.
Hagiwara, Hisahiro; Sugawara, Yoshitaka; Hoshi, Takashi; Suzuki, Toshio. 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, (23): 2942–2944. PMID 15957033. doi:10.1039/b502528a.

nih.gov

ncbi.nlm.nih.gov

Hagiwara, Hisahiro; Sugawara, Yoshitaka; Hoshi, Takashi; Suzuki, Toshio. 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, (23): 2942–2944. PMID 15957033. doi:10.1039/b502528a.

orgsyn.org

Littke, A. F.; Fu, G. C. (2005). "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. 81: 63.

web.archive.org

Lorand Kiss, Tibor Kurtan, Sandor Antus, Henri Brunner. Further insight into the mechanism of Heck oxyarylation in the presence of chiral ligands (free fulltext). Arkivoc. 2003: GB–653J [2010-10-07]. （原始内容存档于2006-05-18）.