Pirol (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Pirol" in Serbian language version.
Last modified:
Ref.Un. Ref.Website
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Serbian rank
6th place
8th place
137th place
172nd place
821st place
451st place
low place
571st place
low place
low place
archive.org (Global: 6th place; Serbian: 8th place)
- Loudon, Marc G. (2002). „Chemistry of Naphthalene and the Aromatic Heterocycles.”. Organic Chemistry (Fourth изд.). New York: Oxford University Press. стр. 1135-1136. ISBN 978-0-19-511999-2.
- Robinson, Gertrude Maud; Robinson, Robert (1918). „LIV.—A new synthesis of tetraphenylpyrrole”. J. Chem. Soc.. 113: 639—645. doi:10.1039/CT9181300639.
books.google.ca (Global: 821st place; Serbian: 451st place)
- Katritzky A.R.; Pozharskii A.F. (2000). Handbook of Heterocyclic Chemistry (Second изд.). Academic Press. ISBN 0080429882.
doi.org (Global: 2nd place; Serbian: 5th place)
- 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.
- 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.
- Harreus, Albrecht Ludwig (2000). „Pyrrole”. Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. ISBN 978-3-527-30385-4. doi:10.1002/14356007.a22_453.
- Oskar Piloty (1910). „Synthese von Pyrrolderivaten: Pyrrole aus Succinylobernsteinsäureester, Pyrrole aus Azinen”. Chem. Ber.. 43: 489—498. doi:10.1002/cber.19100430182.
- Robinson, Gertrude Maud; Robinson, Robert (1918). „LIV.—A new synthesis of tetraphenylpyrrole”. J. Chem. Soc.. 113: 639—645. doi:10.1039/CT9181300639.
- Milgram, Benjamin C.; Eskildsen, Katrine; Richter, Steven M.; W. Robert Scheidt; Karl A. Scheidt (2007). „Microwave-Assisted Piloty-Robinson Synthesis of 3,4-Disubstituted Pyrroles” (Note). J. Org. Chem.. 72 (10): 3941—3944. PMC 1939979
. PMID 17432915. doi:10.1021/jo070389. Непознати параметар |name-list-style=игнорисан (помоћ) - Jose R. Garabatos-Perera; Rotstein, Benjamin H. & Thompson, Alison (2007). „Comparison of Benzene, Nitrobenzene, and Dinitrobenzene 2-Arylsulfenylpyrroles”. J. Org. Chem.. 72 (19): 7382—7385. PMID 17705533. doi:10.1021/jo070493r.
nih.gov (Global: 5th place; Serbian: 7th place)
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.
- Milgram, Benjamin C.; Eskildsen, Katrine; Richter, Steven M.; W. Robert Scheidt; Karl A. Scheidt (2007). „Microwave-Assisted Piloty-Robinson Synthesis of 3,4-Disubstituted Pyrroles” (Note). J. Org. Chem.. 72 (10): 3941—3944. PMC 1939979 . PMID 17432915. doi:10.1021/jo070389. Непознати параметар
|name-list-style=игнорисан (помоћ) - Jose R. Garabatos-Perera; Rotstein, Benjamin H. & Thompson, Alison (2007). „Comparison of Benzene, Nitrobenzene, and Dinitrobenzene 2-Arylsulfenylpyrroles”. J. Org. Chem.. 72 (19): 7382—7385. PMID 17705533. doi:10.1021/jo070493r.
sciencedirect.com (Global: 137th place; Serbian: 172nd place)
- 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.
sciencemadness.org (Global: low place; Serbian: low place)
- Practical Organic Chemistry, Vogel, 1956, Page 837, Link (12 MB)
whfreeman.com (Global: low place; Serbian: 571st place)
- David L. Nelson; Michael M. Cox (2005). Principles of Biochemistry (IV изд.). New York: W. H. Freeman. ISBN 0-7167-4339-6.