Paal–Knorr synthesis (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Paal–Knorr synthesis" in English language version.

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13doi.org

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4zenodo.org

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1harvard.edu

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1nih.gov

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doi.org (Global: 2^nd place; English: 2^nd place)

Paal, C. (1884), "Ueber die Derivate des Acetophenonacetessigesters und des Acetonylacetessigesters", Berichte der deutschen chemischen Gesellschaft, 17 (2): 2756–2767, doi:10.1002/cber.188401702228
Knorr, L. (1884), "Synthese von Furfuranderivaten aus dem Diacetbernsteinsäureester", Berichte der deutschen chemischen Gesellschaft, 17 (2): 2863–2870, doi:10.1002/cber.188401702254
Amarnath, V.; Amarnath, K. (1995), "Intermediates in the Paal-Knorr Synthesis of Furans", The Journal of Organic Chemistry, 60 (2): 301–307, doi:10.1021/jo00107a006
Amarnath, V.; Anthony, D. C.; Amarnath, K.; Valentine, W. M.; Wetterau, L. A.; Graham, D. G. (1991), "Intermediates in the Paal-Knorr synthesis of pyrroles", The Journal of Organic Chemistry, 56 (24): 6924–6931, doi:10.1021/jo00024a040
Campaigne, E.; Foye, W. O. (1952), "The Synthesis of 2,5-Diarylthiophenes", The Journal of Organic Chemistry, 17 (10): 1405–1412, doi:10.1021/jo50010a023
Holman, R. W. (2005), "Strategic Applications of Named Reactions in Organic Synthesis: Background and Detailed Mechanisms (Kürti, László; Czakó, Barbara)", Journal of Chemical Education, 82 (12): 1780, Bibcode:2005JChEd..82S1780H, doi:10.1021/ed082p1780.3
Cormier, R. A.; Francis, M. D. (1981), "The Epoxyketone-Furan Rearrangement", Synthetic Communications, 11 (5): 365, doi:10.1080/00397918108064300
Ji, J.; Lu, X. (1993), "Facile synthesis of 2,5-disubstituted furans via palladium complex and perfluorinated resinsulfonic acid catalysed isomerization–dehydration of alkynediols", Journal of the Chemical Society, Chemical Communications (9): 764–765, doi:10.1039/C39930000764
Minetto, G.; Raveglia, L. F.; Taddei, M. (2004), "Microwave-Assisted Paal−Knorr Reaction. A Rapid Approach to Substituted Pyrroles and Furans", Organic Letters, 6 (3): 389–392, doi:10.1021/ol0362820, PMID 14748600
Knorr, L. (1884), "Synthese von Pyrrolderivaten", Berichte der deutschen chemischen Gesellschaft, 17 (2): 1635–1642, doi:10.1002/cber.18840170220
Knorr, L. (1883), "Einwirkung von Acetessigester auf Phenylhydrazin", Berichte der deutschen chemischen Gesellschaft, 16 (2): 2597–2599, doi:10.1002/cber.188301602194
Trost, B. M.; Doherty, G. A. (2000), "An Asymmetric Synthesis of the Tricyclic Core and a Formal Total Synthesis of Roseophilin via an Enyne Metathesis", Journal of the American Chemical Society, 122 (16): 3801–3810, doi:10.1021/ja9941781
Hart, H.; Takehira, Y. (1982), "Adducts derived from furan macrocycles and benzyne", The Journal of Organic Chemistry, 47 (22): 4370–4372, doi:10.1021/jo00143a049

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Holman, R. W. (2005), "Strategic Applications of Named Reactions in Organic Synthesis: Background and Detailed Mechanisms (Kürti, László; Czakó, Barbara)", Journal of Chemical Education, 82 (12): 1780, Bibcode:2005JChEd..82S1780H, doi:10.1021/ed082p1780.3

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Minetto, G.; Raveglia, L. F.; Taddei, M. (2004), "Microwave-Assisted Paal−Knorr Reaction. A Rapid Approach to Substituted Pyrroles and Furans", Organic Letters, 6 (3): 389–392, doi:10.1021/ol0362820, PMID 14748600

zenodo.org (Global: 621^st place; English: 380^th place)

Paal, C. (1884), "Ueber die Derivate des Acetophenonacetessigesters und des Acetonylacetessigesters", Berichte der deutschen chemischen Gesellschaft, 17 (2): 2756–2767, doi:10.1002/cber.188401702228
Knorr, L. (1884), "Synthese von Furfuranderivaten aus dem Diacetbernsteinsäureester", Berichte der deutschen chemischen Gesellschaft, 17 (2): 2863–2870, doi:10.1002/cber.188401702254
Knorr, L. (1884), "Synthese von Pyrrolderivaten", Berichte der deutschen chemischen Gesellschaft, 17 (2): 1635–1642, doi:10.1002/cber.18840170220
Knorr, L. (1883), "Einwirkung von Acetessigester auf Phenylhydrazin", Berichte der deutschen chemischen Gesellschaft, 16 (2): 2597–2599, doi:10.1002/cber.188301602194

Paal–Knorr synthesis (English Wikipedia)

doi.org (Global: 2nd place; English: 2nd place)

harvard.edu (Global: 18th place; English: 17th place)