Nitrálás (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Nitrálás" in Hungarian language version.

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2web.archive.org

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1^st place

1tankonyvtar.hu

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1chemguide.co.uk

9,416^th place

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1warren-wilson.edu

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chemguide.co.uk

https://www.chemguide.co.uk/organicprops/arenes/nitration.html

doi.org

dx.doi.org

Gerald Booth. Nitro Compounds, Aromatic, Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. DOI: 10.1002/14356007.a17_411 (2007)
(2003) „Unified Mechanism Concept of Electrophilic Aromatic Nitration Revisited: Convergence of Computational Results and Experimental Data”. J. Am. Chem. Soc. 125 (16), 4836–49. o. DOI:10.1021/ja021307w. PMID 12696903.
(2006) „Electrophilic Aromatic Nitration: Understanding Its Mechanism and Substituent Effects”. J. Org. Chem. 71 (16), 6192–203. o. DOI:10.1021/jo0609475. PMID 16872205.
(2010) „Ipso-Nitration of Arenes”. Angewandte Chemie International Edition in English 49 (10), 1726–1728. o. DOI:10.1002/anie.200906940. PMID 20146295.
(1971) „Directive effects in electrophilic aromatic substitution ("ipso factors"). Nitration of haloanisoles”. Journal of the American Chemical Society 93 (14), 3389. o. DOI:10.1021/ja00743a015.
(2009) „Pd-Catalyzed Conversion of Aryl Chlorides, Triflates, and Nonaflates to Nitroaromatics”. DOI:10.1021/ja905768k. PMID 19737014. PMC 2773681.

nih.gov

pubmed.ncbi.nlm.nih.gov

(2003) „Unified Mechanism Concept of Electrophilic Aromatic Nitration Revisited: Convergence of Computational Results and Experimental Data”. J. Am. Chem. Soc. 125 (16), 4836–49. o. DOI:10.1021/ja021307w. PMID 12696903.
(2006) „Electrophilic Aromatic Nitration: Understanding Its Mechanism and Substituent Effects”. J. Org. Chem. 71 (16), 6192–203. o. DOI:10.1021/jo0609475. PMID 16872205.
(2010) „Ipso-Nitration of Arenes”. Angewandte Chemie International Edition in English 49 (10), 1726–1728. o. DOI:10.1002/anie.200906940. PMID 20146295.
(2009) „Pd-Catalyzed Conversion of Aryl Chlorides, Triflates, and Nonaflates to Nitroaromatics”. DOI:10.1021/ja905768k. PMID 19737014. PMC 2773681.

ncbi.nlm.nih.gov

(2009) „Pd-Catalyzed Conversion of Aryl Chlorides, Triflates, and Nonaflates to Nitroaromatics”. DOI:10.1021/ja905768k. PMID 19737014. PMC 2773681.

orgsyn.org

George A. Olah and Stephen J. Kuhn. „Benzonitrile, 2-methyl-3,5-dinitro-”. Org. Synth.. ; Coll. Vol. 5: 480
E. O. Woolfolk and Milton Orchin. „2,4,7-Trinitrofluorenone”. Org. Synth.. ; Coll. Vol. 3: 837
Melvin S. Newman and H. Boden. „2,4,5,7-Tetranitrofluorenone”. Org. Synth.. ; Coll. Vol. 5: 1029

tankonyvtar.hu

regi.tankonyvtar.hu

Antus Sándor, Mátyus Péter. Szerves kémia II. ^{[halott link]}

warren-wilson.edu

Web resource: warren-wilson.edu Archiválva 2012. március 20-i dátummal a Wayback Machine-ben

web.archive.org

Antus Sándor, Mátyus Péter. Szerves kémia II. ^{[halott link]}
Web resource: warren-wilson.edu Archiválva 2012. március 20-i dátummal a Wayback Machine-ben