Diels–Alder reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Diels–Alder reaction" in English language version.

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Zincke, Th.; Meyer, Kurt H. (1909). "Ueber die Umwandlung von Pentenderivaten in Indenderivate" (PDF). Justus Liebigs Annalen der Chemie (in German). 367 (1–2): 1–13. doi:10.1002/jlac.19093670102. ISSN 1099-0690.
Harries, C. (1905). "Zur Kenntniss der Kautschukarten: Ueber Abbau und Constitution des Parakautschuks" (PDF). Berichte der deutschen chemischen Gesellschaft. 38 (1): 1195–1203. doi:10.1002/cber.190503801220. ISSN 1099-0682.
v. Euler, H.; Josephson, K. O. (1920). "Über Kondensationen an Doppelbindungen. I.: Über die Kondensation von Isopren mit Benzochinon" (PDF). Berichte der deutschen chemischen Gesellschaft (A and B Series). 53 (5): 822–826. doi:10.1002/cber.19200530517. ISSN 1099-0682.
Albrecht, Walther (1906). "Additionsproducte von Cyklopentadiën und Chinonen" (PDF). Justus Liebigs Annalen der Chemie (in German). 348 (1–2): 31–49. doi:10.1002/jlac.19063480104. ISSN 1099-0690.

archive.org

Staudinger, Hermann (1912). Die ketene (in German). Stuttgart, F. Enke. p. 58.

books.google.com

Zincke, Th.; Günther, H. (1893). "Ueberführung von Pentenderivaten in Indenderivate". Justus Liebigs Annalen der Chemie (in German). 272 (3): 243–270. doi:10.1002/jlac.18932720302. ISSN 1099-0690.
Zincke, Th. (1897). "Ueber die Einwirkung von Chlor auf o-Amidophenole und o-Diamine". Justus Liebigs Annalen der Chemie (in German). 296 (2): 135–158. doi:10.1002/jlac.18972960202. ISSN 1099-0690.

doi.org

Kloetzel, M. C. (1948). "The Diels–Alder Reaction with Maleic Anhydride". Organic Reactions. Vol. 4. pp. 1–59. doi:10.1002/0471264180.or004.01. ISBN 978-0471264187.
Holmes, H. L. (1948). "The Diels-Alder Reaction Ethylenic and Acetylenic Dienophiles". Organic Reactions. Vol. 4. pp. 60–173. doi:10.1002/0471264180.or004.02. ISBN 978-0471264187.
Nicolaou, K. C.; Snyder, S. A.; Montagnon, T.; Vassilikogiannakis, G. (2002). "The Diels-Alder Reaction in Total Synthesis". Angewandte Chemie International Edition. 41 (10): 1668–1698. doi:10.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z. PMID 19750686.
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Houk, K. N.; Lin, Y. T.; Brown, F. K. (1986). "Evidence for the concerted mechanism of the Diels–Alder reaction of butadiene with ethylene". Journal of the American Chemical Society. 108 (3): 554–556. doi:10.1021/ja00263a059. PMID 22175504.
Goldstein, E.; Beno, B.; Houk, K. N. (1996). "Density Functional Theory Prediction of the Relative Energies and Isotope Effects for the Concerted and Stepwise Mechanisms of the Diels−Alder Reaction of Butadiene and Ethylene". Journal of the American Chemical Society. 118 (25): 6036–6043. doi:10.1021/ja9601494.
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Blokzijl, Wilfried; Engberts, Jan B. F. N. (1992). "Initial-State and Transition-State Effects on Diels–Alder Reactions in Water and Mixed Aqueous Solvents". Journal of the American Chemical Society. 114 (13): 5440–5442. doi:10.1021/ja00039a074.
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Houk, K. N.; Luskus, L. J. (1971). "Influence of steric interactions on endo stereoselectivity". Journal of the American Chemical Society. 93 (18): 4606–4607. doi:10.1021/ja00747a052.
Kobuke, Y.; Sugimoto, T.; Furukawa, J.; Fueno, T. (1972). "Role of attractive interactions in endo–exo stereoselectivities of Diels–Alder reactions". Journal of the American Chemical Society. 94 (10): 3633–3635. doi:10.1021/ja00765a066.
Williamson, K. L.; Hsu, Y.-F. L. (1970). "Stereochemistry of the Diels–Alder reaction. II. Lewis acid catalysis of syn-anti isomerism". Journal of the American Chemical Society. 92 (25): 7385–7389. doi:10.1021/ja00728a022.
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Craig, D.; Shipman, J. J.; Fowler, R. B. (1961). "The Rate of Reaction of Maleic Anhydride with 1,3-Dienes as Related to Diene Conformation". Journal of the American Chemical Society. 83 (13): 2885–2891. doi:10.1021/ja01474a023.
Danishefsky, S.; Kitahara, T. (1974). "Useful diene for the Diels–Alder reaction". Journal of the American Chemical Society. 96 (25): 7807–7808. doi:10.1021/ja00832a031.
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Kozmin, S. A.; Rawal, V. H. (1997). "Preparation and Diels−Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes". Journal of Organic Chemistry. 62 (16): 5252–5253. doi:10.1021/jo970438q.
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Roush, W. R. (1991). "Intramolecular Diels–Alder Reactions". In Trost, B. M.; Flemming, I. (eds.). Comprehensive Organic Synthesis. Vol. 5. pp. 513–550. doi:10.1016/B978-0-08-052349-1.00131-1. ISBN 978-0-08-052349-1.
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Vermeeren, Pascal; Hamlin, Trevor A.; Fernández, Israel; Bickelhaupt, F. Matthias (6 April 2020). "How Lewis Acids Catalyze Diels–Alder Reactions". Angewandte Chemie International Edition. 59 (15): 6201–6206. doi:10.1002/anie.201914582. PMC 7187354. PMID 31944503.
Vermeeren, Pascal; Hamlin, Trevor A.; Fernández, Israel; Bickelhaupt, F. Matthias (2020). "Origin of rate enhancement and asynchronicity in iminium catalyzed Diels–Alder reactions". Chemical Science. 11 (31): 8105–8112. doi:10.1039/D0SC02901G. PMC 8163289. PMID 34094173.
Vermeeren, Pascal; Hamlin, Trevor A.; Bickelhaupt, F. Matthias; Fernández, Israel (17 March 2021). "Bifunctional Hydrogen Bond Donor-Catalyzed Diels–Alder Reactions: Origin of Stereoselectivity and Rate Enhancement". Chemistry: A European Journal. 27 (16): 5180–5190. doi:10.1002/chem.202004496. PMC 8049058. PMID 33169912.
Vermeeren, Pascal; Tiezza, Marco Dalla; Dongen, Michelle; Fernández, Israel; Bickelhaupt, F. Matthias; Hamlin, Trevor A. (21 July 2021). "Lewis Acid-Catalyzed Diels-Alder Reactions: Reactivity Trends across the Periodic Table". Chemistry: A European Journal. 27 (41): 10610–10620. doi:10.1002/chem.202100522. PMC 8360170. PMID 33780068.
Vermeeren, Pascal; Hamlin, Trevor A.; Bickelhaupt, F. Matthias (2021). "Origin of asynchronicity in Diels–Alder reactions". Physical Chemistry Chemical Physics. 23 (36): 20095–20106. Bibcode:2021PCCP...2320095V. doi:10.1039/D1CP02456F. PMC 8457343. PMID 34499069.
Hamlin, Trevor A.; Bickelhaupt, F. Matthias; Fernández, Israel (20 April 2021). "The Pauli Repulsion-Lowering Concept in Catalysis" (PDF). Accounts of Chemical Research. 54 (8): 1972–1981. doi:10.1021/acs.accounts.1c00016. hdl:1871.1/a0090b38-9ab8-4c32-9d9a-b3d5de4e5ed3. ISSN 0001-4842. PMID 33759502. S2CID 232337915.
Vermeeren, Pascal; Brinkhuis, Francine; Hamlin, Trevor A.; Bickelhaupt, F. Matthias (April 2020). "How Alkali Cations Catalyze Aromatic Diels-Alder Reactions". Chemistry: An Asian Journal. 15 (7): 1167–1174. doi:10.1002/asia.202000009. PMC 7187256. PMID 32012430.
Hansen, Thomas; Vermeeren, Pascal; Yoshisada, Ryoji; Filippov, Dmitri V.; van der Marel, Gijsbert A.; Codée, Jeroen D. C.; Hamlin, Trevor A. (19 February 2021). "How Lewis Acids Catalyze Ring-Openings of Cyclohexene Oxide". The Journal of Organic Chemistry. 86 (4): 3565–3573. doi:10.1021/acs.joc.0c02955. PMC 7901664. PMID 33538169.
Tiekink, Eveline H.; Vermeeren, Pascal; Bickelhaupt, F. Matthias; Hamlin, Trevor A. (7 October 2021). "How Lewis Acids Catalyze Ene Reactions". European Journal of Organic Chemistry. 2021 (37): 5275–5283. doi:10.1002/ejoc.202101107. hdl:2066/241097. S2CID 239089361.
Vermeeren, Pascal; Hamlin, Trevor A.; Fernández, Israel; Bickelhaupt, F. Matthias (2020). "Origin of rate enhancement and asynchronicity in iminium catalyzed Diels–Alder reactions". Chemical Science. 11 (31): 8105–8112. doi:10.1039/D0SC02901G. PMC 8163289. PMID 34094173.
Vermeeren, Pascal; Hamlin, Trevor A.; Bickelhaupt, F. Matthias; Fernández, Israel (17 March 2021). "Bifunctional Hydrogen Bond Donor-Catalyzed Diels–Alder Reactions: Origin of Stereoselectivity and Rate Enhancement". Chemistry: A European Journal. 27 (16): 5180–5190. doi:10.1002/chem.202004496. PMC 8049058. PMID 33169912.
Vermeeren, Pascal; Tiezza, Marco Dalla; Dongen, Michelle; Fernández, Israel; Bickelhaupt, F. Matthias; Hamlin, Trevor A. (21 July 2021). "Lewis Acid-Catalyzed Diels-Alder Reactions: Reactivity Trends across the Periodic Table". Chemistry: A European Journal. 27 (41): 10610–10620. doi:10.1002/chem.202100522. PMC 8360170. PMID 33780068.
White, James D.; Shaw, Subrata (2011). "cis-2,5-Diaminobicyclo[2.2.2]octane, a New Scaffold for Asymmetric Catalysis via Salen−Metal Complexes". Org. Lett. 13 (9): 2488–91. doi:10.1021/ol2007378. PMID 21462988.
Evans, D. A.; Chapman, K. T.; Bisaha, J. (1988). "Asymmetric Diels–Alder cycloaddition reactions with chiral α,β-unsaturated N-acyloxazolidinones". Journal of the American Chemical Society. 110 (4): 1238–1256. doi:10.1021/ja00212a037.
Corey, E. J.; Loh, T. P. (1991). "First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels–Alder reactions". Journal of the American Chemical Society. 113 (23): 8966–8967. doi:10.1021/ja00023a066.
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- Zincke, Th.; Meyer, Kurt H. (1909). "Ueber die Umwandlung von Pentenderivaten in Indenderivate" (PDF). Justus Liebigs Annalen der Chemie (in German). 367 (1–2): 1–13. doi:10.1002/jlac.19093670102. ISSN 1099-0690.
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- v. Euler, H.; Josephson, K. O. (1920). "Über Kondensationen an Doppelbindungen. I.: Über die Kondensation von Isopren mit Benzochinon" (PDF). Berichte der deutschen chemischen Gesellschaft (A and B Series). 53 (5): 822–826. doi:10.1002/cber.19200530517. ISSN 1099-0682.
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e-heritage.ru

О полимеризации двуэтиленовых углеводородов

handle.net

hdl.handle.net

Hamlin, Trevor A.; Bickelhaupt, F. Matthias; Fernández, Israel (20 April 2021). "The Pauli Repulsion-Lowering Concept in Catalysis" (PDF). Accounts of Chemical Research. 54 (8): 1972–1981. doi:10.1021/acs.accounts.1c00016. hdl:1871.1/a0090b38-9ab8-4c32-9d9a-b3d5de4e5ed3. ISSN 0001-4842. PMID 33759502. S2CID 232337915.
Tiekink, Eveline H.; Vermeeren, Pascal; Bickelhaupt, F. Matthias; Hamlin, Trevor A. (7 October 2021). "How Lewis Acids Catalyze Ene Reactions". European Journal of Organic Chemistry. 2021 (37): 5275–5283. doi:10.1002/ejoc.202101107. hdl:2066/241097. S2CID 239089361.

harvard.edu

ui.adsabs.harvard.edu

Vermeeren, Pascal; Hamlin, Trevor A.; Bickelhaupt, F. Matthias (2021). "Origin of asynchronicity in Diels–Alder reactions". Physical Chemistry Chemical Physics. 23 (36): 20095–20106. Bibcode:2021PCCP...2320095V. doi:10.1039/D1CP02456F. PMC 8457343. PMID 34499069.
Nicolaou, K. C.; Yang, Z.; Liu, J. J.; Ueno, H.; Nantermet, P. G.; Guy, R. K.; Claiborne, C. F.; Renaud, J.; Couladouros, E. A.; Paulvannan, K.; Sorensen, E. J. (1994). "Total synthesis of taxol". Nature. 367 (6464): 630–4. Bibcode:1994Natur.367..630N. doi:10.1038/367630a0. PMID 7906395. S2CID 4371975.

nih.gov

pubmed.ncbi.nlm.nih.gov

Nicolaou, K. C.; Snyder, S. A.; Montagnon, T.; Vassilikogiannakis, G. (2002). "The Diels-Alder Reaction in Total Synthesis". Angewandte Chemie International Edition. 41 (10): 1668–1698. doi:10.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z. PMID 19750686.
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Vermeeren, Pascal; Hamlin, Trevor A.; Fernández, Israel; Bickelhaupt, F. Matthias (6 April 2020). "How Lewis Acids Catalyze Diels–Alder Reactions". Angewandte Chemie International Edition. 59 (15): 6201–6206. doi:10.1002/anie.201914582. PMC 7187354. PMID 31944503.
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