References analysis of the Wikipedia article "Oxazolin" in the Czech version

doi.org (Global: 2^nd place; Czech: 4^th place)

WENKER, H. Syntheses from Ethanolamine. V. Synthesis of Δ2-Oxazoline and of 2,2'-Δ2-Dioxazoline. Journal of the American Chemical Society. 1938, s. 2152–2153. doi:10.1021/ja01276a036.Je zde použita šablona {{Cite journal}} označená jako k „pouze dočasnému použití“.

E. Vedejs; J. W. Grissom. 4-Oxazoline route to stabilized azomethine ylides. Controlled reduction of oxazolium salts. Journal of the American Chemical Society. 1988, s. 3238–3246. doi:10.1021/ja00218a038.

Diego Armesto; Maria J. Ortiz; Rafael Pérez-Ossorio; William M. Horspool. A novel photochemical 1,2-acyl migration in an enol ester. The synthesis of 3-oxazoline derivatives. Tetrahedron Letters. 1983, s. 1197–1200. doi:10.1016/S0040-4039(00)86403-5.

Marcus C. M. Sá; Albert Kascheres. Electronically Mediated Selectivity in Ring Opening of 1-Azirines. The 3-X Mode: Convenient Route to 3-Oxazolines. The Journal of Organic Chemistry. 1996, s. 3749–3752. doi:10.1021/jo9518866. PMID 11667224.

Richard H. Wiley; Leonard L. Bennett. The Chemistry of the Oxazolines. Chemical Reviews. 1949, s. 447–476. doi:10.1021/cr60139a002.

John A. Frump. Oxazolines. Their preparation, reactions, and applications. Chemical Reviews. 1971, s. 483–505. doi:10.1021/cr60273a003.

Thomas G. Gant; A. I. Meyers. The chemistry of 2-oxazolines (1985–present). Tetrahedron. 1994, s. 2297–2360. doi:10.1016/S0040-4020(01)86953-2.

Marian N. Holerca; Virgil Percec. ¹H NMR Spectroscopic Investigation of the Mechanism of 2-Substituted-2-Oxazoline Ring Formation and of the Hydrolysis of the Corresponding Oxazolinium Salts. European Journal of Organic Chemistry. 2000, s. 2257–2263. doi:10.1002/1099-0690(200006)2000:12<2257::AID-EJOC2257>3.0.CO;2-2.

David Evans; Gretchen S. Peterson; Jeffrey S. Johnson; David M. Barnes; Kevin R. Campos; Keith A. Woerpel. n Improved Procedure for the Preparation of 2,2-Bis[2-[4(S)- tert-butyl-1,3-oxazolinylpropane [(S,S)-tert-Butylbis(oxazoline)] and Derived Copper(II) Complexes. The Journal of Organic Chemistry. 1998, s. 4541–4544. doi:10.1021/jo980296f.

Albert I. Meyers; Mark E. Flanagan. 2,2'-Dimethoxy-6-Formylbiphenyl. Organic Syntheses. 1993, s. 107. doi:10.15227/orgsyn.071.0107.

Stephen R. Sardini; Brian M. Stoltz. Discussion Addendum for: Preparation of (S)-tert-ButylPy Ox and Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids. Organic Syntheses. 2021, s. 117–130. doi:10.15227/orgsyn.098.0117. PMID 36247231.

Helmut Vorbrüggen; Konrad Krolikiewicz. A simple synthesis of Δ2-oxazines, Δ2-oxazines, Δ2-thiazolines and 2-substituted benzoxazoles. Tetrahedron. 1993, s. 9353–9372. doi:10.1016/0040-4020(93)80021-K.

Kirsten Schwekendiek; Frank Glorius. Efficient Oxidative Synthesis of 2-Oxazolines. Synthesis. 2006, s. 2996–3002. doi:10.1055/s-2006-950198.

Midori Ishihara; Hideo Togo. Direct oxidative conversion of aldehydes and alcohols to 2-imidazolines and 2-oxazolines using molecular iodine. Tetrahedron. 2007, s. 1474–1480. doi:10.1016/j.tet.2006.11.077.

Helmut Witte; Wolfgang Seeliger. Simple Synthesis of 2-Substituted 2-Oxazolines and 5,6-Dihydro-4H-1,3-oxazines. Angewandte Chemie International Edition in English. 1972, s. 287–288. doi:10.1002/anie.197202871.

Helmut Witte; Wolfgang Seeliger. Cyclische Imidsäureester aus Nitrilen und Aminoalkoholen. Justus Liebigs Annalen der Chemie. 1974, s. 996–1009. doi:10.1002/jlac.197419740615.

Carsten Bolm; Konrad Weickhardt; Margareta Zehnder; Tobias Ranf. Synthesis of Optically Active Bis(2-oxazolines): Crystal Structure of a 1,2-Bis(2-oxazolinyl)benzene ZnCl₂ Complex. Chemische Berichte. 1991, s. 1173–1180. doi:10.1002/cber.19911240532.

A. V. Makarycheva-Mikhailova, V. Y. Kukushkin, A. A. Nazarov, D. A. Garnovskii, A. J. L. Pombeiro, M. Haukka, B. K. Keppler, M. Galanski. Amidines Derived from Pt(IV)-Mediated Nitrile−Amino Alcohol Coupling and Their Zn(II)-Catalyzed Conversion into Oxazolines. Inorganic Chemistry. 2003, s. 2805–2813. doi:10.1021/ic034070t. PMID 12691592.

A. I. Meyers; M. Ann Hanagan; A. L. Mazzu. 2-Oxazolines from Amides via Imidates. Heterocycles. 1981, s. 361. doi:10.3987/S-1981-01-0361.

A. Cornejo, J. M. Fraile, J. I. García, M. J. Gil, V. Martínez-Merino, J. A. Mayoral, E. Pires, I. Villalba. An Efficient and General One-Pot Method for the Synthesis of Chiral Bis(oxazoline) and Pyridine Bis(oxazoline) Ligands. Synlett. 2005, s. 2321–2324. doi:10.1055/s-2005-872672.

Helen C. Aspinall, John Bacsa, Oliver D. Beckingham, Edward G. B. Eden, Nicholas Greeves, Matthew D. Hobbs, Frances Potjewyd, Marc Schmidtmann, Christopher D. Thomas. Adding the right (or left) twist to tris-chelate complexes – coordination chemistry of chiral oxazolylphenolates with M3+ ions (M = Al or lanthanide). Dalton Transactions. 2014, s. 1434–1442. Dostupné online. doi:10.1039/C3DT52366G. PMID 24201227.

Helen A. McManus; Patrick J. Guiry. Recent Developments in the Application of Oxazoline-Containing Ligands in Asymmetric Catalysis. Chemical Reviews. 2004, s. 4151–4202. doi:10.1021/cr040642v. PMID 15352789.

Gráinne C. Hargaden; Patrick J. Guiry. Recent Applications of Oxazoline-Containing Ligands in Asymmetric Catalysis. Chemical Reviews. 2009, s. 2505–2550. doi:10.1021/cr800400z. PMID 19378971.

Yim Fun Loo, Ruairi O'Kane, Anthony C. Jones, Helen C. Aspinall, Richard J. Potter, Paul R. Chalker, Jamie F. Bickley, Stephen Taylor, Lesley M. Smith. Deposition of HfO₂ and ZrO₂ films by liquid injection MOCVD using new monomeric alkoxide precursors. Journal of Materials Chemistry. 2005, s. 1896. doi:10.1039/B417389A.

T. W. Greene. Protective groups in organic synthesis, 2nd ed.. New York: [s.n.], 1991. Dostupné online. doi:10.1039/B417389A. S. 265–266, 433–436.

Shiro Kobayashi; Hiroshi Uyama. Polymerization of cyclic imino ethers: From its discovery to the present state of the art. Journal of Polymer Science Part A: Polymer Chemistry. 2002-01-15, s. 192–209. doi:10.1002/pola.10090. Bibcode 2002JPoSA..40..192K.

Richard Hoogenboom. Poly(2-oxazoline)s: A Polymer Class with Numerous Potential Applications. Angewandte Chemie International Edition. 2009-10-12, s. 7978–7994. doi:10.1002/anie.200901607. PMID 19768817.

Nico Adams; Ulrich S. Schubert. Poly(2-oxazolines) in biological and biomedical application contexts. Advanced Drug Delivery Reviews. 2007, s. 1504–1520. Dostupné online. doi:10.1016/j.addr.2007.08.018. PMID 17904246.

Andrew M. Kelly; Frank Wiesbrock. Strategies for the Synthesis of Poly(2-Oxazoline)-Based Hydrogels. Macromolecular Rapid Communications. 2012-10-15, s. 1632–1647. doi:10.1002/marc.201200333. PMID 22811405.

nih.gov (Global: 4^th place; Czech: 8^th place)

ncbi.nlm.nih.gov

Gráinne C. Hargaden; Patrick J. Guiry. Recent Applications of Oxazoline-Containing Ligands in Asymmetric Catalysis. Chemical Reviews. 2009, s. 2505–2550. doi:10.1021/cr800400z. PMID 19378971.

rsc.org (Global: 2,020^th place; Czech: 1,556^th place)

Oxazolin (Czech Wikipedia)

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cam.ac.uk (Global: 670^th place; Czech: 1,800^th place)

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doi.org (Global: 2^nd place; Czech: 4^th place)

harvard.edu (Global: 18^th place; Czech: 99^th place)

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nih.gov (Global: 4^th place; Czech: 8^th place)

ncbi.nlm.nih.gov

rsc.org (Global: 2,020^th place; Czech: 1,556^th place)

Oxazolin (Czech Wikipedia)

archive.org (Global: 6th place; Czech: 10th place)

cam.ac.uk (Global: 670th place; Czech: 1,800th place)

dspace.cam.ac.uk

doi.org (Global: 2nd place; Czech: 4th place)

harvard.edu (Global: 18th place; Czech: 99th place)

adsabs.harvard.edu

nih.gov (Global: 4th place; Czech: 8th place)

ncbi.nlm.nih.gov

rsc.org (Global: 2,020th place; Czech: 1,556th place)

archive.org (Global: 6^th place; Czech: 10^th place)

cam.ac.uk (Global: 670^th place; Czech: 1,800^th place)

doi.org (Global: 2^nd place; Czech: 4^th place)

harvard.edu (Global: 18^th place; Czech: 99^th place)

nih.gov (Global: 4^th place; Czech: 8^th place)

rsc.org (Global: 2,020^th place; Czech: 1,556^th place)