Estar (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Estar" in Serbian language version.
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amazon.com
- Wiberg, Kenneth B. (1960). Laboratory Technique in Organic Chemistry. McGraw-Hill series in advanced chemistry. New York: McGraw Hill. ASIN B0007ENAMY.
archive.org
- Wiberg, Kenneth B. (1960). Laboratory Technique in Organic Chemistry. McGraw-Hill series in advanced chemistry. New York: McGraw Hill. ASIN B0007ENAMY.
- Kürti, László; Czakó, Barbara (2005). Strategic Applications of Named Reactions in Organic Synthesis
. Burlington; San Diego; London: Elsevier Academic Press. стр. 28. ISBN 978-0-12-369483-6. - Harwood, Laurence M.; Moody, Christopher J. (1989). Experimental Organic Chemistry: Principles and Practice (Illustrated изд.). Wiley-Blackwell. стр. 55–57. ISBN 978-0632020171.
- 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.
- 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.). стр. 932–933. ISBN 978-0073327495.
- House, Herbert O. (1972). Modern Synthetic Reactions. Menlo Park, CA.: W. A. Benjamin. ISBN 0-8053-4501-9.
arquivo.pt
- W. Reusch. „Carboxyl Derivative Reactivity”. Virtual Textbook of Organic Chemistry. Архивирано из оригинала 2016-05-16. г.
bnf.fr
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]. Compt. Rend. (на језику: француски). 140: 1593—1595.
books.google.com
- 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, Handbuch der Chemie, vol. 4: Handbuch der organischen Chemie (vol. 1) (Heidelberg, Baden (Germany): Karl Winter, 1848), page 182.
Original text:
Translation: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.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
- Mander, Peter (2016-09-01). „Le Châtelier’s principle”. carnotcycle (на језику: енглески). Приступљено 2024-09-29.
chem-ilp.net
- „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
degruyter.com
- Kheilová, M.; Štrunc, M. (1995-01-01). „Is the Le Chatelier-Braun Principle Valid in General in Linear Nonequilibrium Thermodynamics?” (на језику: енглески). 20 (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
- 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. (1995-01-01). „Is the Le Chatelier-Braun Principle Valid in General in Linear Nonequilibrium Thermodynamics?” (на језику: енглески). 20 (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.
- Hughes, D. L. (1996). „Progress in the Mitsunobu Reaction. A Review”. Organic Preparations and Procedures International. 28 (2): 127—164. doi:10.1080/00304949609356516.
- 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 DO, Yadav GD. Process intensification and waste minimization using liquid-liquid-liquid triphase transfer catalysis for the synthesis of 2-((benzyloxy)methyl)furan. Molecular Catalysis 2019;466:112–21. https://doi.org/10.1016/j.mcat.2019.01.004
- J. O. Metzger (1998). „Solvent-Free Organic Syntheses”. Angewandte Chemie International Edition. 37 (21): 2975—2978. PMID 29711128. doi:10.1002/(SICI)1521-3773(19981116)37:21<2975::AID-ANIE2975>3.0.CO;2-A.
- Mieczyslaw Makosza (2000). „Phase-transfer catalysis. A general green methodology in organic synthesis”. Pure Appl. Chem. 72 (7): 1399—1403. doi:10.1351/pac200072071399 .
- Finkelstein, Hans (1910). „Darstellung organischer Jodide aus den entsprechenden Bromiden und Chloriden”. Ber. Dtsch. Chem. Ges. (на језику: German). 43 (2): 1528—1532. doi:10.1002/cber.19100430257.
- Ervithayasuporn, V. (2013). „One-pot synthesis of halogen exchanged silsesquioxanes: octakis(3-bromopropyl)octasilsesquioxane and octakis(3-iodopropyl)octasilsesquioxane”. Dalton Trans. 42 (37): 13747—13753. PMID 23907310. doi:10.1039/C3DT51373D.
- B. H. Lipshutz; M. R. Wood; R. Tirado (1999). „Copper-catalyzed Conjugate Addition of Functionalized Organozinc Reagents to α,β-Unsaturated Ketones: Ethyl 5-(3-oxocyclohexyl)pentanoate”. Org. Synth. 76: 252. doi:10.15227/orgsyn.076.0252.
- Streitwieser, A. (1956). „Solvolytic Displacement Reactions at Saturated Carbon Atoms”. Chem. Rev. 56 (4): 571—752. doi:10.1021/cr50010a001.
- Bordwell, F. G.; Brannen, W. T. (1964). „The Effect of the Carbonyl and Related Groups on the Reactivity of Halides in SN2 Reactions”. J. Am. Chem. Soc. 86 (21): 4645—4650. doi:10.1021/ja01075a025.
- Otera, Junzo. (јун 1993). „Transesterification”. Chemical Reviews. 93 (4): 1449—1470. doi:10.1021/cr00020a004.
- Ahmad, Shahbaz; Bühl, Michael (2021-08-04). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 23 (30): 15869—15880. Bibcode:2021PCCP...2315869A. ISSN 1463-9084. PMID 34318843. S2CID 236472958. doi:10.1039/D1CP02426D . hdl:10023/23678 .
- Kiss, Gabor (2001). „Palladium-Catalyzed Reppe Carbonylation”. Chemical Reviews. 101 (11): 3435—3456. PMID 11840990. doi:10.1021/cr010328q.
- „Vinyl Esters”. Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. 2005. стр. 1—16. doi:10.1002/14356007.a27_419.pub2.
- 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.
- Mlynarski, Jacek (2006). „Direct Asymmetric Aldol-Tishchenko Reaction”. European Journal of Organic Chemistry. 2006 (21): 4779—4786. doi:10.1002/ejoc.200600258.
- Hattori, Hideshi (2001). „Solid base catalysts: Generation of basic sites and application to organic synthesis”. Applied Catalysis A: General. 222 (1–2): 247—259. doi:10.1016/S0926-860X(01)00839-0.
- Kamm, O.; Kamm, W. F. (1922). „Benzyl benzoate”. Organic Syntheses. 2: 5. doi:10.15227/orgsyn.002.0005.
- Cope, Arthur (1960). Organic Reaction Volume XI (1 изд.). New York: Wiley-Interscience. ISBN 9780471171270. doi:10.1002/jps.2600500225.
- Wohllebe, J.; Garbisch, E. W. (1977). „Ring Contraction via a Favorskii-Type Rearrangement: Cycloundecanone”. Org. Synth. 56: 107. doi:10.15227/orgsyn.056.0107.; Coll. Vol., 6, стр. 368
- Shioiri, Takayuki; Kawai, Nobutaka (1978). „New methods and reagents in organic synthesis. 2. A facile conversion of alkyl aryl ketones to α-arylalkanoic acids using diphenyl phosphorazidate. Its application to a new synthesis of ibuprofen and naproxen, nonsteroidal antiinflammatory agents”. J. Org. Chem. 43 (14): 2936—2938. doi:10.1021/jo00408a049.
- Hamada, Yasumasa; Shioiri, Takayuki (1982). „Cycloundecanecarboxylic Acid”. Org. Synth. 62: 191. doi:10.15227/orgsyn.062.0191.; Coll. Vol., 7, стр. 135
- Goheen, D. W.; Vaughan, W. R. (1963). „Cyclopentanecarboxylic acid, methyl ester”. Org. Synth. 39: 37. doi:10.15227/orgsyn.039.0037.; Coll. Vol., 4, стр. 594
- Krow, Grant R. (1993). „The Baeyer-Villiger Oxidation of Ketones and Aldehydes”. Organic Reactions. 43 (3): 251—798. ISBN 0471264180. doi:10.1002/0471264180.or043.03.
- „Pinner Reaction”. Comprehensive Organic Name Reactions and Reagents (504): 2237—2240. 2010. ISBN 9780470638859. doi:10.1002/9780470638859.conrr504.
- A. Pinner, F. Klein; Klein (1877). „Umwandlung der Nitrile in Imide”. Berichte der deutschen chemischen Gesellschaft. 10 (2): 1889—1897. doi:10.1002/cber.187701002154.
- A. Pinner, Fr. Klein; Klein (1878). „Umwandlung der Nitrile in Imide”. Berichte der deutschen chemischen Gesellschaft. 11 (2): 1475—1487. doi:10.1002/cber.18780110258.
- A. Pinner (1883). „Ueber die Umwandlung der Nitrile in Imide”. Berichte der deutschen chemischen Gesellschaft. 16 (2): 1643—1655. doi:10.1002/cber.18830160235.
- Roger, R.; Neilson, D. G. (1961). „The Chemistry of Imidates”. Chem. Rev. 61 (2): 179—211. doi:10.1021/cr60210a003.
- Adams, Roger; Thal, A. F. (1922). „Ethyl Phenylacetate”. Organic Syntheses. 2: 27. doi:10.15227/orgsyn.002.0027.
- Elvidge, J. A.; Linstead, R. P. (1954). „Heterocyclic imines and amines. Part III. Succinimidine”. Journal of the Chemical Society (Resumed): 442. doi:10.1039/JR9540000442.
- 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.
- Neumeister, Joachim; Keul, Helmut; Pratap Saxena, Mahendra; Griesbaum, Karl (1978). „Ozone Cleavage of Olefins with Formation of Ester Fragments”. Angewandte Chemie International Edition in English. 17 (12): 939—940. doi:10.1002/anie.197809392.
- 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.
- Yan, M.; Kawamata, Y.; Baran, P. S. (2017). „Synthetic Organic Electrochemistry: Calling All Engineers.”. Angewandte Chemie International Edition. 57 (16): 4149—4155. PMC 5823775 . PMID 28834012. doi:10.1002/anie.201707584.
- Utley, James (1997). „Trends in Organic Electrosynthesis”. Chemical Society Reviews. 26 (3): 157. doi:10.1039/cs9972600157.
- Makhova, Irina V.; Elinson, Michail N.; Nikishin, Gennady I. (1991). „Electrochemical oxidation of ketones in methanol in the presence of alkali metal bromides”. Tetrahedron. 47 (4–5): 895—905. doi:10.1016/S0040-4020(01)87078-2.
- Costales-Rodriquez, R.; Gibon, V.; Verhe, R.; De Greyt, W. (2009), „Chemical and Enzymatic Interesterification of a Blend of Palm Stearin: Soybean Oil for Low Trans-Margarine Formulation.”, J Am Oil Chem Soc, 86 (7): 681—697, doi:10.1007/s11746-009-1395-2
- Emil Fischer, Arthur Speier (1895). „Darstellung der Ester”. Chemische Berichte. 28 (3): 3252—3258. doi:10.1002/cber.189502803176.
- Offenhauer, Robert D. (1964). „The direct esterification of phenols”. Journal of Chemical Education. 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”. Journal of Chemical Education. 57 (7): 527. Bibcode:1980JChEd..57..527H. doi:10.1021/ed057p527.
- Munson, James W. (1992). „Hydroxamic acids”. Ур.: S. Patai. Acid Derivatives (1992), Volume 2. PATAI'S Chemistry of Functional Groups. стр. 849—873. ISBN 9780470772508. doi:10.1002/9780470772508.ch15.
- C. R. Hauser; W. B. Renfrow Jr (1939). „Benzohydroxamic Acid”. Org. Synth. 19: 15. doi:10.15227/orgsyn.019.0015.
- Yale, H. L. (1943). „The Hydroxamic Acids”. Chem. Rev. 33 (3): 209—256. doi:10.1021/cr60106a002.
- Bauer, L.; Exner, O. (1974). „The Chemistry of Hydroxamic Acids and N-Hydroxyimides”. Angew. Chem. Int. Ed. Engl. 13 (6): 376. doi:10.1002/anie.197403761.
- Shioiri, Takayuki (1991). „Degradation Reactions”. Comprehensive Organic Synthesis. 6: 795—828. ISBN 9780080359298. doi:10.1016/B978-0-08-052349-1.00172-4.
- Hauser, C. R.; Renfrow, Jr.., W. B. (1939). „Benzohydroxamic Acid”. Organic Syntheses. 19: 15. doi:10.15227/orgsyn.019.0015.
- Goebel, M. T.; Marvel, C. S. (1933). „The Oxidation of Grignard Reagents”. Journal of the American Chemical Society. 55 (4): 1693—1696. doi:10.1021/ja01331a065.
- Smith, David H. (1999). „Grignard Reactions in "Wet" Ether”. Journal of Chemical Education. 76 (10): 1427. Bibcode:1999JChEd..76.1427S. doi:10.1021/ed076p1427.
- Wang, Zerong, ур. (2009). „109. Bouveault–Blanc Reduction”. Comprehensive Organic Name Reactions and Reagents. стр. 493—496. ISBN 978-0-471-70450-8. doi:10.1002/9780470638859.conrr109.
- Reid, E. E.; Cockerille, F. O.; Meyer, J. D.; Cox, W. M.; Ruhoff, J. R. (1935). „Oleyl Alcohol”. Organic Syntheses. 15: 51. doi:10.15227/orgsyn.015.0051.
- Adkins, Homer; Gillespie, R. H. (1949). „Oleyl alcohol”. Organic Syntheses. 29: 80. doi:10.15227/orgsyn.029.0080.
- Ford, S. G.; Marvel, C. S. (1930). „Lauryl Alcohol”. Organic Syntheses. 10: 62. doi:10.15227/orgsyn.010.0062.
- 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.
- Sakai, Norio; Moriya, Toshimitsu; Konakahara, Takeo (јул 2007). „An Efficient One-Pot Synthesis of Unsymmetrical Ethers: A Directly Reductive Deoxygenation of Esters Using an InBr3/Et3SiH Catalytic System”. The Journal of Organic Chemistry. 72 (15): 5920—5922. PMID 17602594. doi:10.1021/jo070814z.
- Claisen, L.; Claparede, A. (1881). „Condensationen von Ketonen mit Aldehyden”. Berichte der Deutschen Chemischen Gesellschaft. 14 (2): 2460—2468. doi:10.1002/cber.188101402192.
- Claisen, L. (1887). „Ueber die Einführung von Säureradicalen in Ketone”. Berichte der Deutschen Chemischen Gesellschaft. 20 (1): 655—657. doi:10.1002/cber.188702001150.
- 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.
- Riemenschneider, Wilhelm; Bolt, Hermann M. (2005). „Esters, Organic”. Ullmann's Encyclopedia of Industrial Chemistry. ISBN 3527306730. doi:10.1002/14356007.a09_565.pub2.
- Kwart, Harold; King, Kenneth (1969). „Rearrangement and cyclization reactions of carboxylic acids and esters”. Ур.: S. Patai. PATAI'S Chemistry of Functional Groups: Carboxylic Acids and Esters (1969). стр. 341—373. ISBN 9780470771099. doi:10.1002/9780470771099.ch8.
- Schaefer, J. P.; Bloomfield, J. J. (1967). „The Dieckmann Condensation (Including the Thorpe-Ziegler Condensation)”. Organic Reactions. 15: 1—203. ISBN 0471264180. doi:10.1002/0471264180.or015.01.
- Baker, W. (1933). „Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones”. J. Chem. Soc.: 1381—1389. doi:10.1039/JR9330001381.
- Mahal, H. S.; Venkataraman, K. (1934). „Synthetical experiments in the chromone. group. XIV. Action of sodamide on 1-acyloxy-2-acetonaphthones”. J. Chem. Soc.: 1767—1769. doi:10.1039/JR9340001767.
- Wheeler, T. S. (1952). „Flavone”. Organic Syntheses. 32: 72. doi:10.15227/orgsyn.032.0072. (also in the Collective Volume (1963) 4: 478 (PDF)).
- 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.
- Kraus, G. A.; Fulton, B. S.; Wood, S.H. (1984). „Aliphatic acyl transfer in the Baker-Venkataraman reaction”. J. Org. Chem. 49 (17): 3212—3214. doi:10.1021/jo00191a033.
- Reddy, B.P.; Krupadanam, G.L.D. (1996). „The synthesis of 8-allyl-2-styrylchromones by the modified baker-venkataraman transformation”. J. Heterocycl. Chem. 33 (6): 1561. doi:10.1002/jhet.5570330602.
- 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.
- Santos, C.M.M.; Silva, A.M.S.; Cavaleiro, J.A.S. (2003). „Synthesis of New Hydroxy-2-styrylchromones”. Eur. J. Org. Chem. 2003 (23): 4575. doi:10.1002/ejoc.200300468. hdl:10198/3932 .
- Santos, Clementina M.; Silva, Artur M. S. (2017). „An Overview of 2-Styrylchromones: Natural Occurrence,Synthesis, Reactivity and Biological Properties”. Eur. J. Org. Chem. 2017 (22): 3115—3133. doi:10.1002/ejoc.201700003. hdl:10198/14517 — преко Reaxys.
- Rearrangement of α-acyloxyacetates into 2-hydroxy-3-ketoesters S. D. Lee, T. H. Chan, and K. S. Kwon Tetrahedron Lett. 1984, 25, 3399-3402. (doi:10.1016/S0040-4039(01)91030-5)
- First total synthesis of taxol 1. Functionalization of the B ring Robert A. Holton, Carmen Somoza, Hyeong Baik Kim, Feng Liang, Ronald J. Biediger, P. Douglas Boatman, Mitsuru Shindo, Chase C. Smith, Soekchan Kim, et al.; J. Am. Chem. Soc. 1994, 116(4), 1597-1598. (doi:10.1021/ja00083a066)
- Fráter, G.; Müller, U.; Günther, W. (1984). „The stereoselective α-alkylation of chiral β-hydroxy esters and some applications thereof”. Tetrahedron. 40 (8): 1269—1277. doi:10.1016/S0040-4020(01)82413-3.
- Seebach, Dieter; Wasmuth, Daniel (1980). „Herstellung von erythro-2-Hydroxybernsteinsäure-Derivaten aus Äpfelsäureester. Vorläufige Mitteilung”. Helvetica Chimica Acta (на језику: German). 63 (1): 197—200. doi:10.1002/hlca.19800630118.
- Crimmins, Michael; Vanier, Grace (2006). „Enantioselective Total Synthesis of (+)-SCH 351448”. Organic Letters. 8 (13): 2887—2890. PMID 16774282. doi:10.1021/ol061073b.
- Raghavan, Sadagopan; Rathore, Kailash (2009). „Asymmetric synthesis of (−)-tetrahydrolipstatin”. Tetrahedron. 65 (48): 10083—10092. doi:10.1016/j.tet.2009.09.062.
- Wood, J. L.; Khatri, N. A.; Weinreb, S. M. (1979). „A direct conversion of esters to nitriles”. Tetrahedron Letters. 20 (51): 4907. doi:10.1016/S0040-4039(01)86746-0.
- Poon, Po. S.; Banerjee, Ajoy K.; Laya, Manuel S. (2011). „Advances in the Krapcho Decarboxylation”. Journal of Chemical Research (на језику: енглески). 35 (2): 67—73. ISSN 1747-5198. doi:10.3184/174751911X12964930076403.
- Hansen, Thomas; Roozee, Jasper C.; Bickelhaupt, F. Matthias; Hamlin, Trevor A. (2022-02-04). „How Solvation Influences the S N 2 versus E2 Competition”. The Journal of Organic Chemistry (на језику: енглески). 87 (3): 1805—1813. ISSN 0022-3263. PMC 8822482 . PMID 34932346. doi:10.1021/acs.joc.1c02354.
- Olejar, Kenneth J.; Kinney, Chad A. (2021). „Evaluation of thermo-chemical conversion temperatures of cannabinoid acids in hemp (Cannabis sativa L.) biomass by pressurized liquid extraction”. Journal of Cannabis Research (на језику: енглески). 3 (1): 40. ISSN 2522-5782. PMC 8408919 . PMID 34465400. doi:10.1186/s42238-021-00098-6 .
- Dunn, Gerald E.; Thimm, Harald F. (1977-04-15). „Kinetics and mechanism of decarboxylation of some pyridinecarboxylic acids in aqueous solution. II”. Canadian Journal of Chemistry (на језику: енглески). 55 (8): 1342—1347. ISSN 0008-4042. doi:10.1139/v77-185.
- Krapcho, A. Paul; Weimaster, J. F.; Eldridge, J. M.; Jahngen, E. G. E.; Lovey, A. J.; Stephens, W. P. (1978-01-01). „Synthetic applications and mechanism studies of the decarbalkoxylations of geminal diesters and related systems effected in dimethyl sulfoxide by water and/or by water with added salts”. The Journal of Organic Chemistry. 43 (1): 138—147. ISSN 0022-3263. doi:10.1021/jo00395a032.
- Fries, K.; Finck, G. (1908). „Über Homologe des Cumaranons und ihre Abkömmlinge”. Chemische Berichte. 41 (3): 4271—4284. doi:10.1002/cber.190804103146.
- Fries, K.; Pfaffendorf, W. (1910). „Über ein Kondensationsprodukt des Cumaranons und seine Umwandlung in Oxindirubin”. Chemische Berichte. 43 (1): 212—219. doi:10.1002/cber.19100430131.
- Finley, K. T. (1964). „The Acyloin Condensation as a Cyclization Method”. Chem. Rev. 64 (5): 573—589. doi:10.1021/cr60231a004.
expasy.org
enzyme.expasy.org
- „ENZYME – 3.1.1.3 Triacylglycerol lipase”. enzyme.expasy.org. SIB Swiss Institute of Bioinformatics. Приступљено 2021-02-17.
handle.net
hdl.handle.net
- 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 (2021-08-04). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 23 (30): 15869—15880. Bibcode:2021PCCP...2315869A. ISSN 1463-9084. PMID 34318843. S2CID 236472958. doi:10.1039/D1CP02426D . hdl:10023/23678 .
- Santos, C.M.M.; Silva, A.M.S.; Cavaleiro, J.A.S. (2003). „Synthesis of New Hydroxy-2-styrylchromones”. Eur. J. Org. Chem. 2003 (23): 4575. doi:10.1002/ejoc.200300468. hdl:10198/3932 .
- Santos, Clementina M.; Silva, Artur M. S. (2017). „An Overview of 2-Styrylchromones: Natural Occurrence,Synthesis, Reactivity and Biological Properties”. Eur. J. Org. Chem. 2017 (22): 3115—3133. doi:10.1002/ejoc.201700003. hdl:10198/14517 — преко Reaxys.
harvard.edu
adsabs.harvard.edu
- 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 (2021-08-04). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 23 (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”. Journal of Chemical Education. 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”. Journal of Chemical Education. 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.
iastate.edu
lib.dr.iastate.edu
- Kraus, G. A.; Fulton, B. S.; Wood, S.H. (1984). „Aliphatic acyl transfer in the Baker-Venkataraman reaction”. J. Org. Chem. 49 (17): 3212—3214. doi:10.1021/jo00191a033.
iseo.org
- Institute of Shortenings and Edible oils (2006). „Food Fats and oils” (PDF). Архивирано из оригинала (PDF) 2007-03-26. г. Приступљено 2009-02-19.
jst.go.jp
jlc.jst.go.jp
- 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 .
mpob.gov.my
palmoilis.mpob.gov.my
- 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.
msu.edu
cem.msu.edu
- W. Reusch. „Carboxyl Derivative Reactivity”. Virtual Textbook of Organic Chemistry. Архивирано из оригинала 2016-05-16. г.
nih.gov
ncbi.nlm.nih.gov
- 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.
- 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.
- 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.
- 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 .
- J. O. Metzger (1998). „Solvent-Free Organic Syntheses”. Angewandte Chemie International Edition. 37 (21): 2975—2978. PMID 29711128. doi:10.1002/(SICI)1521-3773(19981116)37:21<2975::AID-ANIE2975>3.0.CO;2-A.
- Ervithayasuporn, V. (2013). „One-pot synthesis of halogen exchanged silsesquioxanes: octakis(3-bromopropyl)octasilsesquioxane and octakis(3-iodopropyl)octasilsesquioxane”. Dalton Trans. 42 (37): 13747—13753. PMID 23907310. doi:10.1039/C3DT51373D.
- Ahmad, Shahbaz; Bühl, Michael (2021-08-04). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 23 (30): 15869—15880. Bibcode:2021PCCP...2315869A. ISSN 1463-9084. PMID 34318843. S2CID 236472958. doi:10.1039/D1CP02426D . hdl:10023/23678 .
- Kiss, Gabor (2001). „Palladium-Catalyzed Reppe Carbonylation”. Chemical Reviews. 101 (11): 3435—3456. PMID 11840990. doi:10.1021/cr010328q.
- 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.
- Yan, M.; Kawamata, Y.; Baran, P. S. (2017). „Synthetic Organic Electrochemistry: Calling All Engineers.”. Angewandte Chemie International Edition. 57 (16): 4149—4155. PMC 5823775 . PMID 28834012. doi:10.1002/anie.201707584.
- Sakai, Norio; Moriya, Toshimitsu; Konakahara, Takeo (јул 2007). „An Efficient One-Pot Synthesis of Unsymmetrical Ethers: A Directly Reductive Deoxygenation of Esters Using an InBr3/Et3SiH Catalytic System”. The Journal of Organic Chemistry. 72 (15): 5920—5922. PMID 17602594. doi:10.1021/jo070814z.
- Crimmins, Michael; Vanier, Grace (2006). „Enantioselective Total Synthesis of (+)-SCH 351448”. Organic Letters. 8 (13): 2887—2890. PMID 16774282. doi:10.1021/ol061073b.
- Hansen, Thomas; Roozee, Jasper C.; Bickelhaupt, F. Matthias; Hamlin, Trevor A. (2022-02-04). „How Solvation Influences the S N 2 versus E2 Competition”. The Journal of Organic Chemistry (на језику: енглески). 87 (3): 1805—1813. ISSN 0022-3263. PMC 8822482 . PMID 34932346. doi:10.1021/acs.joc.1c02354.
- Olejar, Kenneth J.; Kinney, Chad A. (2021). „Evaluation of thermo-chemical conversion temperatures of cannabinoid acids in hemp (Cannabis sativa L.) biomass by pressurized liquid extraction”. Journal of Cannabis Research (на језику: енглески). 3 (1): 40. ISSN 2522-5782. PMC 8408919 . PMID 34465400. doi:10.1186/s42238-021-00098-6 .
pubchem.ncbi.nlm.nih.gov
nrcresearchpress.com
- Dunn, Gerald E.; Thimm, Harald F. (1977-04-15). „Kinetics and mechanism of decarboxylation of some pyridinecarboxylic acids in aqueous solution. II”. Canadian Journal of Chemistry (на језику: енглески). 55 (8): 1342—1347. ISSN 0008-4042. doi:10.1139/v77-185.
opentextbc.ca
- Ball, David W.; Key, Jessie A. (2014-09-16). „Shifting Equilibria: Le Chatelier’s Principle”. Introductory Chemistry – 1st Canadian edition (на језику: енглески). Victoria, B.C: BCcampus: OpenEd. ISBN 978-1-77420-003-2 — преко opentextbc.ca.
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.
- „Malonic Ester Synthesis”. Organic Chemistry Portal. Приступљено 2007-10-26.
orgsyn.org
- B. Neises; W. Steglich. „Esterification of Carboxylic Acids with Dicyclohexylcarbodiimide/4-Dimethylaminopyridine: tert-Butyl ethyl fumarate”. Org. Synth.; Coll. Vol., 7, стр. 93
- „Organic Syntheses Procedure”. orgsyn.org (на језику: енглески). Приступљено 2023-02-13.
- Wohllebe, J.; Garbisch, E. W. (1977). „Ring Contraction via a Favorskii-Type Rearrangement: Cycloundecanone”. Org. Synth. 56: 107. doi:10.15227/orgsyn.056.0107.; Coll. Vol., 6, стр. 368
- Hamada, Yasumasa; Shioiri, Takayuki (1982). „Cycloundecanecarboxylic Acid”. Org. Synth. 62: 191. doi:10.15227/orgsyn.062.0191.; Coll. Vol., 7, стр. 135
- Goheen, D. W.; Vaughan, W. R. (1963). „Cyclopentanecarboxylic acid, methyl ester”. Org. Synth. 39: 37. doi:10.15227/orgsyn.039.0037.; Coll. Vol., 4, стр. 594
- Bailey, P. S.; Erickson, R. E. (1973). „Diphenaldehyde”. Org. Synth.; Coll. Vol., 5, стр. 489
- Tietze, L. F.; Bratz, M. (1998). „Dialkyl Mesoxalates by Ozonolysis of Dialkyl Benzalmalonates”. Org. Synth.; Coll. Vol., 9, стр. 314
- Wheeler, T. S. (1952). „Flavone”. Organic Syntheses. 32: 72. doi:10.15227/orgsyn.032.0072. (also in the Collective Volume (1963) 4: 478 (PDF)).
- Organic Syntheses, Coll. Vol. 3, p.30 (1955); Vol. 29, p.2 (1949). Link
- Organic Syntheses, Coll. Vol. 4, p.746 (1963); Vol. 38, p.78 (1958). Link
- Organic Syntheses, Coll. Vol. 5, p.235 (1973); Vol. 43, p.17 (1963). Link
orgsynth.org
- Isolation of triglyceride from nutmeg: G. D. Beal "Trimyristen" Organic Syntheses, Coll. Vol. 1, p.538 (1941). Link
pharmaxchange.info
- „Chemistry of Enols and Enolates - Acidity of alpha-hydrogens”. Архивирано из оригинала 07. 01. 2018. г. Приступљено 25. 11. 2011.
rsc.org
- Andrea Sella (јун 2010). „Classic kit: Dean–Stark apparatus”. Chemistry World. Royal Society of Chemistry.
sagepub.com
journals.sagepub.com
- Poon, Po. S.; Banerjee, Ajoy K.; Laya, Manuel S. (2011). „Advances in the Krapcho Decarboxylation”. Journal of Chemical Research (на језику: енглески). 35 (2): 67—73. ISSN 1747-5198. doi:10.3184/174751911X12964930076403.
scribd.com
- 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
api.semanticscholar.org
- Ahmad, Shahbaz; Bühl, Michael (2021-08-04). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 23 (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
- Helmenstine, Anne Marie (2020). „Le Chatelier's Principle Definition”. ThoughtCo. Архивирано из оригинала 2021-04-20. г. Приступљено 2022-03-09.
ugent.be
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
- „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.
wikipedia.org
en.wikipedia.org
- 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 .
- Wiberg, Kenneth B. (1960). Laboratory Technique in Organic Chemistry. McGraw-Hill series in advanced chemistry. New York: McGraw Hill. ASIN B0007ENAMY.
- Ahmad, Shahbaz; Bühl, Michael (2021-08-04). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 23 (30): 15869—15880. Bibcode:2021PCCP...2315869A. ISSN 1463-9084. PMID 34318843. S2CID 236472958. doi:10.1039/D1CP02426D . hdl:10023/23678 .
- Santos, C.M.M.; Silva, A.M.S.; Cavaleiro, J.A.S. (2003). „Synthesis of New Hydroxy-2-styrylchromones”. Eur. J. Org. Chem. 2003 (23): 4575. doi:10.1002/ejoc.200300468. hdl:10198/3932 .
- Santos, Clementina M.; Silva, Artur M. S. (2017). „An Overview of 2-Styrylchromones: Natural Occurrence,Synthesis, Reactivity and Biological Properties”. Eur. J. Org. Chem. 2017 (22): 3115—3133. doi:10.1002/ejoc.201700003. hdl:10198/14517 — преко Reaxys.
fr.wikipedia.org
worldcat.org
- Kheilová, M.; Štrunc, M. (1995-01-01). „Is the Le Chatelier-Braun Principle Valid in General in Linear Nonequilibrium Thermodynamics?” (на језику: енглески). 20 (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 (2021-08-04). „Computational modelling of Pd-catalysed alkoxycarbonylation of alkenes and alkynes”. Physical Chemistry Chemical Physics (на језику: енглески). 23 (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). 35 (2): 67—73. ISSN 1747-5198. doi:10.3184/174751911X12964930076403.
- Hansen, Thomas; Roozee, Jasper C.; Bickelhaupt, F. Matthias; Hamlin, Trevor A. (2022-02-04). „How Solvation Influences the S N 2 versus E2 Competition”. The Journal of Organic Chemistry (на језику: енглески). 87 (3): 1805—1813. ISSN 0022-3263. PMC 8822482 . PMID 34932346. doi:10.1021/acs.joc.1c02354.
- Olejar, Kenneth J.; Kinney, Chad A. (2021). „Evaluation of thermo-chemical conversion temperatures of cannabinoid acids in hemp (Cannabis sativa L.) biomass by pressurized liquid extraction”. Journal of Cannabis Research (на језику: енглески). 3 (1): 40. ISSN 2522-5782. PMC 8408919 . PMID 34465400. doi:10.1186/s42238-021-00098-6 .
- Dunn, Gerald E.; Thimm, Harald F. (1977-04-15). „Kinetics and mechanism of decarboxylation of some pyridinecarboxylic acids in aqueous solution. II”. Canadian Journal of Chemistry (на језику: енглески). 55 (8): 1342—1347. ISSN 0008-4042. doi:10.1139/v77-185.
- Krapcho, A. Paul; Weimaster, J. F.; Eldridge, J. M.; Jahngen, E. G. E.; Lovey, A. J.; Stephens, W. P. (1978-01-01). „Synthetic applications and mechanism studies of the decarbalkoxylations of geminal diesters and related systems effected in dimethyl sulfoxide by water and/or by water with added salts”. The Journal of Organic Chemistry. 43 (1): 138—147. ISSN 0022-3263. doi:10.1021/jo00395a032.
zenodo.org
- Finkelstein, Hans (1910). „Darstellung organischer Jodide aus den entsprechenden Bromiden und Chloriden”. Ber. Dtsch. Chem. Ges. (на језику: German). 43 (2): 1528—1532. doi:10.1002/cber.19100430257.
- A. Pinner, F. Klein; Klein (1877). „Umwandlung der Nitrile in Imide”. Berichte der deutschen chemischen Gesellschaft. 10 (2): 1889—1897. doi:10.1002/cber.187701002154.
- A. Pinner, Fr. Klein; Klein (1878). „Umwandlung der Nitrile in Imide”. Berichte der deutschen chemischen Gesellschaft. 11 (2): 1475—1487. doi:10.1002/cber.18780110258.
- A. Pinner (1883). „Ueber die Umwandlung der Nitrile in Imide”. Berichte der deutschen chemischen Gesellschaft. 16 (2): 1643—1655. doi:10.1002/cber.18830160235.
- Claisen, L. (1887). „Ueber die Einführung von Säureradicalen in Ketone”. Berichte der Deutschen Chemischen Gesellschaft. 20 (1): 655—657. doi:10.1002/cber.188702001150.
- Fries, K.; Finck, G. (1908). „Über Homologe des Cumaranons und ihre Abkömmlinge”. Chemische Berichte. 41 (3): 4271—4284. doi:10.1002/cber.190804103146.
- Fries, K.; Pfaffendorf, W. (1910). „Über ein Kondensationsprodukt des Cumaranons und seine Umwandlung in Oxindirubin”. Chemische Berichte. 43 (1): 212—219. doi:10.1002/cber.19100430131.