Heck reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Heck reaction" in English language version.

refsWebsite

Global rank English rank

15doi.org

2^nd place

5nih.gov

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3harvard.edu

18^th place

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2arkat-usa.org

low place

1acs.org

1,248^th place

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1orgsyn.org

2,971^st place

2,826^th place

acs.org

pubs.acs.org

Drahl, Carmen (May 17, 2010). "In Names, History And Legacy". Chem. Eng. News. 88 (22): 31–33. doi:10.1021/cen-v088n020.p031. Retrieved June 4, 2011.

arkat-usa.org

Lorand Kiss; Tibor Kurtan; Sandor Antus; Henri Brunner (2003). "Further insight into the mechanism of Heck oxyarylation in the presence of chiral ligands". Arkivoc: GB–653J.
Mitsuru Kitamura; Daisuke Kudo; Koichi Narasaka (2005). "Palladium(0)-catalyzed synthesis of pyridines from β-acetoxy-γ,δ-unsaturated ketone oximes". Arkivoc: JC–1563E.

doi.org

Drahl, Carmen (May 17, 2010). "In Names, History And Legacy". Chem. Eng. News. 88 (22): 31–33. doi:10.1021/cen-v088n020.p031. Retrieved June 4, 2011.
Heck, R. F. (1982). "Palladium-catalyzed vinylation of organic halides". Org. React. 27: 345–390. doi:10.1002/0471264180.or027.02. ISBN 978-0471264187.
de Meijere, A.; Meyer, F. E. (1994). "Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb". Angew. Chem. Int. Ed. Engl. 33 (2324): 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 (8): 3009–3066. doi:10.1021/cr9903048. PMID 11749313.
Mc Cartney, Dennis; Guiry, Patrick J. (2011). "The asymmetric Heck and related reactions". Chem. Soc. Rev. 40 (10): 5122–5150. doi:10.1039/C1CS15101K. PMID 21677934.
Moritani, Ichiro; Fujiwara, Yuzo (1967). "Aromatic substitution of styrene-palladium chloride complex". Tetrahedron Lett. 8 (12): 1119–1122. doi:10.1016/S0040-4039(00)90648-8.
Fujiwara, Yuzo; Noritani, Ichiro; Danno, Sadao; Asano, Ryuzo; Teranishi, Shiichiro (1969). "Aromatic substitution of olefins. VI. Arylation of olefins with palladium(II) acetate". J. Am. Chem. Soc. 91 (25): 7166–9. Bibcode:1969JAChS..91.7166F. doi:10.1021/ja01053a047. PMID 27462934.
Richard F. Heck (1969). "Mechanism of Arylation and Carbomethoxylation of Olefins with Organopalladium Compounds". J. Am. Chem. Soc. 91 (24): 6707–6714. Bibcode:1969JAChS..91.6707H. doi:10.1021/ja01052a029.
Heck, R. F.; Nolley, 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.
Mizoroki, T.; Mori, K.; Ozaki, A. (1971). "Arylation of Olefin with Aryl Iodide Catalyzed by Palladium". Bull. Chem. Soc. Jpn. 44 (2): 581. doi:10.1246/bcsj.44.581.
Dieck, H. A.; Heck, R. F. (1974). "Organophosphinepalladium complexes as catalysts for vinylic hydrogen substitution reactions". J. Am. Chem. Soc. 96 (4): 1133. Bibcode:1974JAChS..96.1133D. 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 Letters. 21 (11): 2177–2180. doi:10.1246/cl.1992.2177.
Bradshaw, Michael; Zou, Jianli; Byrne, Lindsay; Swaminathan Iyer, K.; Stewart, Scott G.; Raston, Colin L. (2011). "Pd(II) conjugated chitosan nanofibre mats for application in Heck cross-coupling reactions". Chem. Commun. 47 (45): 12292–12294. doi:10.1039/C1CC14717J. PMID 22011792.
De Vries; Johannes G. (2001). "The Heck reaction in the production of fine chemicals". Can. J. Chem. 79 (5–6): 1086. doi:10.1139/cjc-79-5-6-1086.
Hagiwara, Hisahiro; Sugawara, Yoshitaka; Hoshi, Takashi; Suzuki, Toshio (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". Chem. Commun. (23): 2942–2944. doi:10.1039/b502528a. PMID 15957033.

harvard.edu

ui.adsabs.harvard.edu

Fujiwara, Yuzo; Noritani, Ichiro; Danno, Sadao; Asano, Ryuzo; Teranishi, Shiichiro (1969). "Aromatic substitution of olefins. VI. Arylation of olefins with palladium(II) acetate". J. Am. Chem. Soc. 91 (25): 7166–9. Bibcode:1969JAChS..91.7166F. doi:10.1021/ja01053a047. PMID 27462934.
Richard F. Heck (1969). "Mechanism of Arylation and Carbomethoxylation of Olefins with Organopalladium Compounds". J. Am. Chem. Soc. 91 (24): 6707–6714. Bibcode:1969JAChS..91.6707H. 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 (4): 1133. Bibcode:1974JAChS..96.1133D. doi:10.1021/ja00811a029.

nih.gov

pubmed.ncbi.nlm.nih.gov

Beletskaya, I. P.; Cheprakov, A. V. (2000). "The Heck Reaction as a Sharpening Stone of Palladium Catalysis". Chem. Rev. 100 (8): 3009–3066. doi:10.1021/cr9903048. PMID 11749313.
Mc Cartney, Dennis; Guiry, Patrick J. (2011). "The asymmetric Heck and related reactions". Chem. Soc. Rev. 40 (10): 5122–5150. doi:10.1039/C1CS15101K. PMID 21677934.
Fujiwara, Yuzo; Noritani, Ichiro; Danno, Sadao; Asano, Ryuzo; Teranishi, Shiichiro (1969). "Aromatic substitution of olefins. VI. Arylation of olefins with palladium(II) acetate". J. Am. Chem. Soc. 91 (25): 7166–9. Bibcode:1969JAChS..91.7166F. doi:10.1021/ja01053a047. PMID 27462934.
Bradshaw, Michael; Zou, Jianli; Byrne, Lindsay; Swaminathan Iyer, K.; Stewart, Scott G.; Raston, Colin L. (2011). "Pd(II) conjugated chitosan nanofibre mats for application in Heck cross-coupling reactions". Chem. Commun. 47 (45): 12292–12294. doi:10.1039/C1CC14717J. PMID 22011792.
Hagiwara, Hisahiro; Sugawara, Yoshitaka; Hoshi, Takashi; Suzuki, Toshio (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". Chem. Commun. (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-phenylacryacid butyl ester and (E)-4-(2-phenylethenyl)benzonitrile". Organic Syntheses. 81: 63.