Estar (Serbian Wikipedia)

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

Last modified: 02:00:55, 14 August 2026 (UTC)

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De Vos, Lobke; Van de Voorde, Babs; Van Daele, Lenny; Dubruel, Peter; Van Vlierberghe, Sandra (децембар 2021). „Poly(alkylene terephthalate)s: From current developments in synthetic strategies towards applications”. European Polymer Journal. 161: 110840. Bibcode:2021EurPJ.16110840D. doi:10.1016/j.eurpolymj.2021.110840. hdl:1854/LU-8730084 .
Ahmad, Shahbaz; Bühl, Michael (2021). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 2021-08-04 (30): 15869—15880. Bibcode:2021PCCP...2315869A. ISSN 1463-9084. PMID 34318843. S2CID 236472958. doi:10.1039/D1CP02426D . hdl:10023/23678 .
Offenhauer, Robert D. (1964). „The direct esterification of phenols”. 41 (1): 39. Bibcode:1964JChEd..41...39O. doi:10.1021/ed041p39.
Hocking, M.B. (1980). „Phenyl acetate preparation from phenol and acetic acid: Reassessment of a common textbook misconception”. 57 (7): 527. Bibcode:1980JChEd..57..527H. doi:10.1021/ed057p527.
Smith, David H. (1999). „Grignard Reactions in "Wet" Ether”. Journal of Chemical Education. 76 (10): 1427. Bibcode:1999JChEd..76.1427S. doi:10.1021/ed076p1427.

amazon.com (Global: 159^th place; Serbian: 246^th place)

Wiberg, Kenneth B. (1960). Laboratory Technique in Organic Chemistry. McGraw-Hill series in advanced chemistry. New York: McGraw Hill. ASIN B0007ENAMY.

archive.org (Global: 6^th place; Serbian: 8^th place)

Hunter G. K. (2000). Vital Forces. The discovery of the molecular basis of life. London: Academic Press. 2000. ISBN 978-0-12-361811-5.
Wiberg, Kenneth B. (1960). Laboratory Technique in Organic Chemistry. McGraw-Hill series in advanced chemistry. New York: McGraw Hill. ASIN B0007ENAMY.
Mitsunobu, O.; Yamada, Y. (1967). „Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium Salts”. Bulletin of the Chemical Society of Japan. 40 (10): 2380—2382. doi:10.1246/bcsj.40.2380.
Mitsunobu, O. (1981). „The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products”. Synthesis. 1981 (1): 1—28. doi:10.1055/s-1981-29317.
Swamy, K. C. K.; Kumar, N. N. B.; Balaraman, E.; Kumar, K. V. P. P. (2009). „Mitsunobu and Related Reactions: Advances and Applications”. Chemical Reviews. 109 (6): 2551—2651. PMID 19382806. doi:10.1021/cr800278z.
Seki, Tsunetake; Nakajo, Tetsuo; Onaka, Makoto (2006). „The Tishchenko Reaction: A Classic and Practical Tool for Ester Synthesis”. Chemistry Letters. 35 (8): 824—829. doi:10.1246/cl.2006.824.
Carey, Francis A.; Sundberg, Richard J. (2007). Advanced Organic Chemistry: Part B: Reactions and Synthesis (5th изд.). New York: Springer. стр. 1135. ISBN 978-0387683546.
Spessard, Gary O.; Miessler, Gary L. (2010). Organometallic Chemistry. Oxford University Press. стр. 285–289. ISBN 978-0-19-533099-1.
Harwood, Laurence M.; Moody, Christopher J. (1989). Experimental Organic Chemistry: Principles and Practice (Illustrated изд.). Wiley-Blackwell. стр. 55–57. ISBN 978-0632020171.
Sperry, Jeffrey B.; Wright, Dennis L. (2006). „The application of cathodic reductions and anodic oxidations in the synthesis of complex molecules”. Chem. Soc. Rev.. 35 (7): 605—621. PMID 16791332. doi:10.1039/b512308a.
Utley, James (1997). „Trends in Organic Electrosynthesis”. Chemical Society Reviews. 26 (3): 157. doi:10.1039/cs9972600157.
Furniss, Brian; Hannaford, Antony; Smith, Peter; Tatchell, Austin (1996). Vogel's Textbook of Practical Organic Chemistry 5th Ed.. London: Longman Science & Technical. стр. 695–697 & 699–704. ISBN 9780582462366.
Smith, David H. (1999). „Grignard Reactions in "Wet" Ether”. Journal of Chemical Education. 76 (10): 1427. Bibcode:1999JChEd..76.1427S. doi:10.1021/ed076p1427.
Yato, Michihisa; Homma, Koichi; Ishida, Akihiko (јун 2001). „Reduction of carboxylic esters to ethers with triethyl silane in the combined use of titanium tetrachloride and trimethylsilyl trifluoromethanesulfonate”. Tetrahedron. 57 (25): 5353—5359. doi:10.1016/S0040-4020(01)00420-3.
Carey, F. A. (2006). Organic Chemistry (6th изд.). New York, NY: McGraw-Hill. ISBN 0-07-111562-5.
Janice Gorzynski Smith (2007). Organic Chemistry (2nd изд.). McGraw-Hill. стр. 932–933. ISBN 978-0073327495.
Jain, P. K.; Makrandi, J. K. (1982). „A Facile Baker-Venkataraman Synthesis of Flavones using Phase Transfer Catalysis”. Synthesis. 1982 (3): 221—222. doi:10.1055/s-1982-29755.
Kalinin, A. V.; Da Silva, A. J. M.; Lopes, C. C.; Lopes, R. S. C.; Snieckus, V. (1998). „Directed ortho metalation – cross coupling links. Carbamoyl rendition of the Baker-Venkataraman rearrangement. Regiospecific route to substituted 4-hydroxycoumarins”. Tetrahedron Letters. 39 (28): 4995—4998. doi:10.1016/S0040-4039(98)00977-0.
Kalinin, A.V.; Sneckus, V. (1998). „4,6-Dimethoxy-3,7-dimethylcoumarin from Colchicum decaisnei. Total synthesis by carbamoyl Baker-Venkataraman rearrangement and structural revision to isoeugenetin methyl ether”. Tetrahedron Lett.. 39 (28): 4999. doi:10.1016/S0040-4039(98)00978-2.
Thasana, N.; Ruchirawat, S. (2002). „The application of the Baker–Venkataraman rearrangement to the synthesis of benz[b]indeno[2,1-e]pyran-10,11-dione”. Tetrahedron Lett.. 43 (25): 4515. doi:10.1016/S0040-4039(02)00818-3.
House, Herbert O. (1972). Modern Synthetic Reactions. Menlo Park, CA.: W. A. Benjamin. ISBN 0-8053-4501-9.

arquivo.pt (Global: 2,454^th place; Serbian: 1,926^th place)

W. Reusch. „Carboxyl Derivative Reactivity”. Virtual Textbook of Organic Chemistry. Архивирано из оригинала 2016-05-16. г..

bnf.fr (Global: 61^st place; Serbian: 598^th place)

gallica.bnf.fr

Bouveault, L.; Blanc, G. (1903). „Préparation des alcools primaires au moyen des acides correspondants” [Preparation of primary alcohols by means of the corresponding acids]. Compt. Rend. (на језику: French). 136: 1676—1678.
Bouveault, L.; Blanc, G. (1904). „Transformation des acides monobasiques saturés dans les alcools primaires correspondants” [Transforming saturated monobasic acids into the corresponding primary alcohols]. Bull. Soc. Chim. Fr. (на језику: French). 31: 666—672.
Bouveault, L.; Blanc, G. (1904). „Hydrogénation des éthers des acides possédant en outre les fonctions éther-oxyde ou acétal” [Hydrogenation of the ether of the acids furthermore possessing the ether-oxide or acetal functions]. Bull. Soc. Chim. Fr. (на језику: French). 31 (3): 1210—1213.
Claisen, L.; Claparede, A. (1881). „Condensationen von Ketonen mit Aldehyden”. Berichte der Deutschen Chemischen Gesellschaft. 14 (2): 2460—2468. doi:10.1002/cber.188101402192.
Bouveault, L.; Locquin, R. (1905). „Action du sodium sur les éthers des acides monobasiques à fonction simple de la série grasse” [Effect of sodium on the ethers of single-function monobasic acids of the fatty series] (на језику: француски). 140: 1593—1595.

books.google.com (Global: 3^rd place; Serbian: 10^th place)

Cameron Wright (1986). A worker's guide to solvent hazards. The Group. стр. 48. ISBN 9780969054542.
E. Richard Booser (21. 12. 1993). CRC Handbook of Lubrication and Tribology, Volume III: Monitoring, Materials, Synthetic Lubricants, and Applications. CRC. стр. 237. ISBN 978-1-4200-5045-5.
Leopold Gmelin (1848). Handbuch der Chemie, vol. 4: Handbuch der organischen Chemie. стр. 182. . (vol. 1) (Heidelberg, Baden. (Germany): Karl Winter), [1].
Original text:
b. Ester oder sauerstoffsäure Aetherarten.
Ethers du troisième genre.

Viele mineralische und organische Sauerstoffsäuren treten mit einer Alkohol-Art unter Ausscheidung von Wasser zu neutralen flüchtigen ätherischen Verbindungen zusammen, welche man als gepaarte Verbindungen von Alkohol und Säuren-Wasser oder, nach der Radicaltheorie, als Salze betrachten kann, in welchen eine Säure mit einem Aether verbunden ist.
Translation:
b. Ester or oxy-acid ethers.
Ethers of the third type.

Many mineral and organic acids containing oxygen combine with an alcohol upon elimination of water to [form] neutral, volatile ether compounds, which one can view as coupled compounds of alcohol and acid-water, or, according to the theory of radicals, as salts in which an acid is bonded with an ether.
Smith, Michael B.; March, Jerry (2007). Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th изд.). New York: Wiley-Interscience. ISBN 0-471-72091-7.
E. W. Dean and D. D. Stark (1920). „A convenient method for the determination of water in petroleum and other organic emulsions”. The Journal of Industrial & Engineering Chemistry. 12 (5): 486—490. doi:10.1021/ie50125a025.
Tingle, J. Bishop (1906). „Reports: Esterification”. American Chemical Journal. 35: 368—369. Приступљено 19. 1. 2016.
Philip E. Rakita (1996). „5. Safe Handling Practices of Industrial Scale Grignard Ragents” (Google Books excerpt). Ур.: Gary S. Silverman; Philip E. Rakita. Handbook of Grignard reagents. CRC Press. стр. 79—88. ISBN 0-8247-9545-8.

carnotcycle.wordpress.com (Global: low place; Serbian: low place)

Mander, Peter (2016-09-01). „Le Châtelier's principle”. carnotcycle (на језику: енглески). Приступљено 2024-09-29.

chem-ilp.net (Global: low place; Serbian: low place)

„Dean–Stark Apparatus”. University of Southampton, University of Birmingham, University of Nottingham and University of Sheffield. Архивирано из оригинала 8. 9. 2011. г. Приступљено 17. 11. 2011.

chemspider.com (Global: 6,145^th place; Serbian: low place)

„Trimethyltin acetate | C5H12O2Sn | ChemSpider”.

degruyter.com (Global: 927^th place; Serbian: 874^th place)

Kheilová, M.; Štrunc, M. (1995). „Is the Le Chatelier-Braun Principle Valid in General in Linear Nonequilibrium Thermodynamics?”. Journal of Non-Equilibrium Thermodynamics (на језику: енглески). 1995-01-01 (1): 19—38. ISSN 1437-4358. doi:10.1515/jnet.1995.20.1.19.
Ignatyev, Igor; Charlie Van Doorslaer; Pascal G.N. Mertens; Koen Binnemans; Dirk. E. de Vos (2011). „Synthesis of glucose esters from cellulose in ionic liquids”. Holzforschung. 66 (4): 417—425. S2CID 101737591. doi:10.1515/hf.2011.161.

doi.org (Global: 2^nd place; Serbian: 5^th place)

A. A. Yakovenko; J. H. Gallegos; M. Yu. Antipin; A. Masunov; T. V. Timofeeva (2011). „Crystal Morphology as an Evidence of Supramolecular Organization in Adducts of 1,2-Bis(chloromercurio)tetrafluorobenzene with Organic Esters”. Crystal Growth & Design. 11 (9): 3964—3978. doi:10.1021/cg200547k.
Diwakar M. Pawar; Abdelnaser A. Khalil; Denise R. Hooks; Kenneth Collins; Tijuana Elliott; Jefforey Stafford; Lucille Smith; Eric A. Noe (1998). „E and Z Conformations of Esters, Thiol Esters, and Amides”. Journal of the American Chemical Society. 120 (9): 2108—2112. doi:10.1021/ja9723848.
Christophe Dugave; Luc Demange (2003). „Cis−Trans Isomerization of Organic Molecules and Biomolecules: Implications and Applications”. Chemical Reviews. 103 (7): 2475—2932. PMID 12848578. doi:10.1021/cr0104375.
De Vos, Lobke; Van de Voorde, Babs; Van Daele, Lenny; Dubruel, Peter; Van Vlierberghe, Sandra (децембар 2021). „Poly(alkylene terephthalate)s: From current developments in synthetic strategies towards applications”. European Polymer Journal. 161: 110840. Bibcode:2021EurPJ.16110840D. doi:10.1016/j.eurpolymj.2021.110840. hdl:1854/LU-8730084 .
Takashi Ohara; Takahisa Sato; Noboru Shimizu; Günter Prescher; Helmut Schwind; Otto Weiberg; Klaus Marten; Helmut Greim (2003). „Acrylic Acid and Derivatives”. Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. ISBN 3527306730. doi:10.1002/14356007.a01_161.pub2.
„Esters, Organic”. Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. 2005. doi:10.1002/14356007.a09_565.pub2.
Williams, Roger J.; Gabriel, Alton; Andrews, Roy C. (1928). „The Relation Between the Hydrolysis Equilibrium Constant of Esters and the Strengths of the Corresponding Acids”. Journal of the American Chemical Society. 50 (5): 1267—1271. doi:10.1021/ja01392a005.
Kheilová, M.; Štrunc, M. (1995). „Is the Le Chatelier-Braun Principle Valid in General in Linear Nonequilibrium Thermodynamics?”. Journal of Non-Equilibrium Thermodynamics (на језику: енглески). 1995-01-01 (1): 19—38. ISSN 1437-4358. doi:10.1515/jnet.1995.20.1.19.
Kresge, Charles T.; Dhingra, Sandeep S. (2004). „Molecular Sieves”. Kirk-Othmer Encyclopedia of Chemical Technology. ISBN 978-0-471-48494-3. doi:10.1002/0471238961.1315120511210812.a01.pub2.
Mazur, Michal; Přech, Jan; Čejka, Jiří (2019). „Zeolites and Other Micro- and Mesoporous Molecular Sieves”. Kirk-Othmer Encyclopedia of Chemical Technology. стр. 1—36. ISBN 978-0-471-48494-3. doi:10.1002/0471238961.zeolcejk.a01.pub2.
Cohen, Alan P. (2003). „Desiccants”. Kirk-Othmer Encyclopedia of Chemical Technology. ISBN 978-0-471-48494-3. doi:10.1002/0471238961.0405190903150805.a01.pub2.
E. W. Dean and D. D. Stark (1920). „A convenient method for the determination of water in petroleum and other organic emulsions”. The Journal of Industrial & Engineering Chemistry. 12 (5): 486—490. doi:10.1021/ie50125a025.
B. Neises, W. Steglich (1978). „Simple Method for the Esterification of Carboxylic Acids”. Angew. Chem. Int. Ed.. 17 (7): 522—524. doi:10.1002/anie.197805221.
J. C. Sheehan, G. P. Hess (1955). „A New Method of Forming Peptide Bonds”. J. Am. Chem. Soc.. 77 (4): 1067—1068. doi:10.1021/ja01609a099.
W. König, R. Geiger (1970). „Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1-Hydroxy-benzotriazolen”. Chem. Ber.. 103 (3): 788—798. PMID 5436656. doi:10.1002/cber.19701030319.
Mitsunobu, O.; Yamada, Y. (1967). „Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium Salts”. Bulletin of the Chemical Society of Japan. 40 (10): 2380—2382. doi:10.1246/bcsj.40.2380.
Mitsunobu, O. (1981). „The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products”. Synthesis. 1981 (1): 1—28. doi:10.1055/s-1981-29317.
Castro, B. R. (1983). „Replacement of Alcoholic Hydroxyl Groups by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates”. Replacement of Alcoholic Hydroxy Groups by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates. Organic Reactions. 29. стр. 1—162. ISBN 9780471264187. doi:10.1002/0471264180.or029.01.
Hughes, D. L. (1992). „The Mitsunobu Reaction”. Organic Reactions. 42. стр. 335—656. ISBN 9780471264187. doi:10.1002/0471264180.or042.02.
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Swamy, K. C. K.; Kumar, N. N. B.; Balaraman, E.; Kumar, K. V. P. P. (2009). „Mitsunobu and Related Reactions: Advances and Applications”. Chemical Reviews. 109 (6): 2551—2651. PMID 19382806. doi:10.1021/cr800278z.
Raber, Douglas J.; Gariano, Jr, Patrick; Brod, Albert O.; Gariano, Anne L.; Guida, Wayne C. (1977). „Esterification of Carboxylic Acids with Trialkyloxonium Salts: Ethyl and Methyl 4-Acetoxybenzoates”. Organic Syntheses. 56: 59. doi:10.15227/orgsyn.056.0059.
Matsumoto, Kouichi; Shimazaki, Hayato; Miyamoto, Yu; Shimada, Kazuaki; Haga, Fumi; Yamada, Yuki; Miyazawa, Hirotsugu; Nishiwaki, Keiji; Kashimura, Shigenori (2014). „Simple and Convenient Synthesis of Esters from Carboxylic Acids and Alkyl Halides Using Tetrabutylammonium Fluoride”. Journal of Oleo Science (на језику: енглески). 63 (5): 539—544. ISSN 1345-8957. PMID 24770480. doi:10.5650/jos.ess13199 .
Katole, Dhiraj O.; Yadav, Ganapati D. (2019). „Process intensification and waste minimization using liquid-liquid-liquid tri-phase transfer catalysis for the synthesis of 2-((benzyloxy)methyl)furan”. Molecular Catalysis. 466: 112—21. doi:10.1016/j.mcat.2019.01.004.
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scribd.com (Global: 467^th place; Serbian: 82^nd place)

Hauser, C. R.; Hudson, B. E. Jr. (1942). „The Acetoacetic Ester Condensation and Certain Related Reactions”. Organic Reactions. 1: 266—302. ISBN 0471264180. doi:10.1002/0471264180.or001.09.

semanticscholar.org (Global: 15^th place; Serbian: 34^th place)

api.semanticscholar.org

Ahmad, Shahbaz; Bühl, Michael (2021). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 2021-08-04 (30): 15869—15880. Bibcode:2021PCCP...2315869A. ISSN 1463-9084. PMID 34318843. S2CID 236472958. doi:10.1039/D1CP02426D . hdl:10023/23678 .
Ignatyev, Igor; Charlie Van Doorslaer; Pascal G.N. Mertens; Koen Binnemans; Dirk. E. de Vos (2011). „Synthesis of glucose esters from cellulose in ionic liquids”. Holzforschung. 66 (4): 417—425. S2CID 101737591. doi:10.1515/hf.2011.161.

thoughtco.com (Global: 2,170^th place; Serbian: 1,149^th place)

Helmenstine, Anne Marie (2020). „Le Chatelier's Principle Definition”. ThoughtCo. Архивирано из оригинала 2021-04-20. г. Приступљено 2022-03-09.

ugent.be (Global: 3,681^st place; Serbian: 4,497^th place)

biblio.ugent.be

De Vos, Lobke; Van de Voorde, Babs; Van Daele, Lenny; Dubruel, Peter; Van Vlierberghe, Sandra (децембар 2021). „Poly(alkylene terephthalate)s: From current developments in synthetic strategies towards applications”. European Polymer Journal. 161: 110840. Bibcode:2021EurPJ.16110840D. doi:10.1016/j.eurpolymj.2021.110840. hdl:1854/LU-8730084 .

web.archive.org (Global: 1^st place; Serbian: 2^nd place)

„Chemistry of Enols and Enolates - Acidity of alpha-hydrogens”. Архивирано из оригинала 07. 01. 2018. г. Приступљено 25. 11. 2011.
Helmenstine, Anne Marie (2020). „Le Chatelier's Principle Definition”. ThoughtCo. Архивирано из оригинала 2021-04-20. г. Приступљено 2022-03-09.
„Dean–Stark Apparatus”. University of Southampton, University of Birmingham, University of Nottingham and University of Sheffield. Архивирано из оригинала 8. 9. 2011. г. Приступљено 17. 11. 2011.
T. L. Husum, L. S. Pedersen, P. M. Nielsen, M. W. Christensen, D. Kristensen, and H. C. Holm (2003): "Enzymatic interesterification: Process advantages and product benefits." Архивирано 2006-01-04 на сајту Wayback Machine . Palm Oil Information Online Service. Retrieved 2010-10-20.
Institute of Shortenings and Edible oils (2006). „Food Fats and oils” (PDF). Архивирано из оригинала (PDF) 2007-03-26. г. Приступљено 2009-02-19.

worldcat.org (Global: 4^th place; Serbian: 11^th place)

Kheilová, M.; Štrunc, M. (1995). „Is the Le Chatelier-Braun Principle Valid in General in Linear Nonequilibrium Thermodynamics?”. Journal of Non-Equilibrium Thermodynamics (на језику: енглески). 1995-01-01 (1): 19—38. ISSN 1437-4358. doi:10.1515/jnet.1995.20.1.19.
Matsumoto, Kouichi; Shimazaki, Hayato; Miyamoto, Yu; Shimada, Kazuaki; Haga, Fumi; Yamada, Yuki; Miyazawa, Hirotsugu; Nishiwaki, Keiji; Kashimura, Shigenori (2014). „Simple and Convenient Synthesis of Esters from Carboxylic Acids and Alkyl Halides Using Tetrabutylammonium Fluoride”. Journal of Oleo Science (на језику: енглески). 63 (5): 539—544. ISSN 1345-8957. PMID 24770480. doi:10.5650/jos.ess13199 .
Ahmad, Shahbaz; Bühl, Michael (2021). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 2021-08-04 (30): 15869—15880. Bibcode:2021PCCP...2315869A. ISSN 1463-9084. PMID 34318843. S2CID 236472958. doi:10.1039/D1CP02426D . hdl:10023/23678 .
Poon, Po. S.; Banerjee, Ajoy K.; Laya, Manuel S. (2011). „Advances in the Krapcho Decarboxylation”. Journal of Chemical Research (на језику: енглески) (2): 67—73. ISSN 1747-5198. doi:10.3184/174751911X12964930076403.
Hansen, Thomas; Roozee, Jasper C.; Bickelhaupt, F. Matthias; Hamlin, Trevor A.. „How Solvation Influences the S N 2 versus E2 Competition”. The Journal of Organic Chemistry (на језику: енглески). 2022-02-04 (3): 1805—1813. ISSN 0022-3263. PMC 8822482 . PMID 34932346. doi:10.1021/acs.joc.1c02354.
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