ヘック反応 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ヘック反応" in Japanese language version.

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13doi.org

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2arkat-usa.org

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arkat-usa.org

Kiss, L.; Kurtan, T.; Antus, S.; Brunner, H. (2003). “Further insight into the mechanism of Heck oxyarylation in the presence of chiral ligands” (PDF). Arkivoc: GB–653J.
Kitamura, M.; Kudo, D.; Narasaka, K. (2005). “Palladium(0)-catalyzed synthesis of pyridines from β-acetoxy-γ,δ-unsaturated ketone oximes” (PDF). Arkivoc: JC–1563E.

doi.org

Mizoroki, T.; Mori, K.; Ozaki, A. (1971). “Arylation of Olefin with Aryl Iodide Catalyzed by Palladium”. Bull. Chem. Soc. Jap. 44: 581. doi:10.1246/bcsj.44.581.
Heck, R. F.; Nolley, Jr., J. P. (1972). “Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides”. J. Org. Chem. 37 (14): 2320–2322. doi:10.1021/jo00979a024.
Heck, R. F. (1982). “Palladium-Catalyzed Vinylation of Organic Halides”. Org. React. 27: 345–390. doi:10.1002/0471264180.or027.02.
A. de Meijere, F. E. Meyer, Jr.; (1994). “Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb”. Angew. Chem. Int. Ed. Engl. 33: 2379–2411. doi:10.1002/anie.199423791.
Beletskaya, I. P.; Cheprakov, A. V. (2000). “The Heck Reaction as a Sharpening Stone of Palladium Catalysis”. Chem. Rev. 100: 3009–3066. doi:10.1021/cr9903048.
Fujiwara, Y.; Noritani, I.; Danno, S.; Asano, R.; Teranishi, S. (1969). “Aromatic substitution of olefins. VI. Arylation of olefins with palladium(II) acetate”. J. Am. Chem. Soc. 91: 7166. doi:10.1021/ja01053a047.
Heck, R. F. (1969). “Mechanism of arylation and carbomethoxylation of olefins with organopalladium compounds”. J. Am. Chem. Soc. 91: 6707. doi:10.1021/ja01052a029.
Dieck, H. A.; Heck, R. F. (1974). “Organophosphinepalladium complexes as catalysts for vinylic hydrogen substitution reactions”. J. Am. Chem. Soc. 96: 1133. doi:10.1021/ja00811a029.
Ozawa, F.; Kubo, A.; Hayashi, T. (1992). “Generation of Tertiary Phosphine-Coordinated Pd(0) Species from Pd(OAc)2 in the Catalytic Heck Reaction”. Chemistry Lett.: 2177–2180. doi:10.1246/cl.1992.2177.
De Vries, J. G. (2001). “The Heck reaction in the production of fine chemicals”. Can. J. Chem. 79: 1086. doi:10.1139/cjc-79-5-6-1086.
Dounay, A. B.; Overman, L. E. (2003). “The asymmetric intramolecular Heck reaction in natural product total synthesis”. Chem. Rev. 103 (8): 2945–2964. doi:10.1021/cr020039h.
Shibasaki, M.; Vogl, E. M.; Ohshima, T. (2004). “Asymmetric Heck reaction”. Adv. Synth. Catal. 346: 1533–1552. doi:10.1002/adsc.200404203.
Hagiwara, H.; Sugawara, Y.; Hoshi, T.; Suzuki, T. (2005). “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 (23): 2942–2944. doi:10.1039/b502528a. PMID 15957033.

nih.gov

pubmed.ncbi.nlm.nih.gov

Hagiwara, H.; Sugawara, Y.; Hoshi, T.; Suzuki, T. (2005). “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 (23): 2942–2944. doi:10.1039/b502528a. PMID 15957033.

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". Organic Syntheses (英語). 81: 63.

wikipedia.org

en.wikipedia.org

Beletskaya, I. P.; Cheprakov, A. V. (2000). “The Heck Reaction as a Sharpening Stone of Palladium Catalysis”. Chem. Rev. 100: 3009–3066. doi:10.1021/cr9903048.
Kitamura, M.; Kudo, D.; Narasaka, K. (2005). “Palladium(0)-catalyzed synthesis of pyridines from β-acetoxy-γ,δ-unsaturated ketone oximes” (PDF). Arkivoc: JC–1563E.