Indol (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Indol" in Serbian language version.

refsWebsite

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1sciencedirect.com

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1organic-chemistry.org

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doi.org

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
Gribble G. W. (2000). „Recent developments in indole ring synthesis—methodology and applications”. J. Chem. Soc. Perkin Trans. 1 (7): 1045. doi:10.1039/a909834h.
Cacchi, S.; Fabrizi, G. (2005). „Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions”. Chem. Rev. 105 (7): 2873. PMID 16011327. doi:10.1021/cr040639b.
Humphrey, G. R.; Kuethe, J. T. (2006). „Practical Methodologies for the Synthesis of Indoles”. Chem. Rev. 106 (7): 2875. PMID 16836303. doi:10.1021/cr0505270.
Gerd Collin and Hartmut Höke “Indole” Ullmann's Encyclopedia of Industrial Chemistry 2002, . Weinheim: Wiley-VCH. doi:10.1002/14356007.a14_167. Недостаје или је празан параметар |title= (помоћ).

google.ca

books.google.ca

Katritzky A.R.; Pozharskii A.F. (2000). Handbook of Heterocyclic Chemistry (Second изд.). Academic Press. ISBN 0080429882.

leffingwell.com

„Recent Events in Olfactory Understanding”.

nih.gov

ncbi.nlm.nih.gov

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Cacchi, S.; Fabrizi, G. (2005). „Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions”. Chem. Rev. 105 (7): 2873. PMID 16011327. doi:10.1021/cr040639b.
Humphrey, G. R.; Kuethe, J. T. (2006). „Practical Methodologies for the Synthesis of Indoles”. Chem. Rev. 106 (7): 2875. PMID 16836303. doi:10.1021/cr0505270.

organic-chemistry.org

Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (I изд.). Oxford University Press. ISBN 978-0-19-850346-0.

orgsyn.org

James, P. N.; Snyder, H. R. (1959). „Indole-3-aldehyde”. Organic Syntheses. 39: 30—.
Heaney, H.; Ley, S. V. (1974). „1-Benzylindole”. Organic Syntheses. 54: 58—.

sciencedirect.com

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

wikipedia.org

sr.wikipedia.org

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

wiley.com

onlinelibrary.wiley.com

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.