References analysis of the Wikipedia article "Diels–Alder reaction" in the English version

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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.

Atilla Tasdelen, Mehmet (2011). "Diels–Alder "click" reactions: recent applications in polymer and material science". Polymer Chemistry. 2 (10): 2133–2145. doi:10.1039/C1PY00041A.

Dewar, M. J.; Olivella, S.; Stewart, J. J. (1986). "Mechanism of the Diels-Alder reaction: Reactions of butadiene with ethylene and cyanoethylenes". Journal of the American Chemical Society. 108 (19): 5771–5779. doi:10.1021/ja00279a018. PMID 22175326.

Gajewski, J. J.; Peterson, K. B.; Kagel, J. R. (1987). "Transition-state structure variation in the Diels–Alder reaction from secondary deuterium kinetic isotope effects: The reaction of a nearly symmetrical diene and dienophile is nearly synchronous". Journal of the American Chemical Society. 109 (18): 5545–5546. doi:10.1021/ja00252a052.

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.

Breslow, R.; Guo, T. (1988). "Diels-Alder reactions in nonaqueous polar solvents. Kinetic effects of chaotropic and antichaotropic agents and of β-cyclodextrin". Journal of the American Chemical Society. 110 (17): 5613–5617. doi:10.1021/ja00225a003.

Rideout, D. C.; Breslow, R. (1980). "Hydrophobic acceleration of Diels-Alder reactions". Journal of the American Chemical Society. 102 (26): 7816–7817. doi:10.1021/ja00546a048.

Breslow, R.; Rizzo, C. J. (1991). "Chaotropic salt effects in a hydrophobically accelerated Diels–Alder reaction". Journal of the American Chemical Society. 113 (11): 4340–4341. doi:10.1021/ja00011a052.

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.

Ashby, E. C.; Chao, L.-C.; Neumann, H. M. (1973). "Organometallic reaction mechanisms. XII. Mechanism of methylmagnesium bromide addition to benzonitrile". Journal of the American Chemical Society. 95 (15): 4896–4904. doi:10.1021/ja00796a022.

Kirmse, W.; Mönch, D. (1991). "Umlagerungen von 1,4,4- und 2,2,5-Trimethylbicyclo[3.2.1]oct-6-yl-Kationen". Chemische Berichte. 124 (1): 237–240. doi:10.1002/cber.19911240136.

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.

Wannere, Chaitanya S.; Paul, Ankan; Herges, Rainer; Houk, K. N.; Schaefer, Henry F.; Schleyer, Paul Von Ragué (2007). "The existence of secondary orbital interactions". Journal of Computational Chemistry. 28 (1): 344–361. doi:10.1002/jcc.20532. ISSN 1096-987X. PMID 17109435. S2CID 26096085.

Backer, H. J. (1939). "Le 2,3-Ditertiobutylbutadiène". Recueil des Travaux Chimiques des Pays-Bas. 58 (7): 643–661. doi:10.1002/recl.19390580712.

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.

Savard, J.; Brassard, P. (1979). "Regiospecific syntheses of quinones using vinylketene acetals derived from unsaturated esters". Tetrahedron Letters. 20 (51): 4911–4914. doi:10.1016/S0040-4039(01)86747-2.

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.

Ranganathan, S.; Ranganathan, D.; Mehrotra, A. K. (1977). "Ketene Equivalents". Synthesis. 1977 (5): 289–296. doi:10.1055/s-1977-24362. S2CID 260335918.

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.

Grieco, P. A.; Larsen, S. D. (1990). "Iminium Ion-Based Diels–Alder Reactions: N-Benzyl-2-Azanorborene" (PDF). Organic Syntheses. 68: 206. doi:10.15227/orgsyn.068.0206.

Houk, Kendall N. (1 November 1975). "Frontier molecular orbital theory of cycloaddition reactions". Accounts of Chemical Research. 8 (11): 361–369. doi:10.1021/ar50095a001. ISSN 0001-4842.

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.

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.

Corey, E. J.; Shibata, T.; Lee, T. W. (2002). "Asymmetric Diels-Alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine". Journal of the American Chemical Society. 124 (15): 3808–3809. doi:10.1021/ja025848x. PMID 11942799.

Ryu, D. H.; Corey, E. J. (2003). "Triflimide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition". Journal of the American Chemical Society. 125 (21): 6388–6390. doi:10.1021/ja035393r. PMID 12785777.

Johnson, J. S.; Evans, D. A. (2000). "Chiral bis(oxazoline) copper(II) complexes: Versatile catalysts for enantioselective cycloaddition, Aldol, Michael, and carbonyl Ene reactions". Accounts of Chemical Research. 33 (6): 325–335. doi:10.1021/ar960062n. PMID 10891050.

Ahrendt, K. A.; Borths, C. J.; MacMillan, D. W. C. (2000). "New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction". Journal of the American Chemical Society. 122 (17): 4243–4244. doi:10.1021/ja000092s.

Hoye, T. R.; Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P. (2012). "The hexadehydro-Diels–Alder reaction". Nature. 490 (7419): 208–212. doi:10.1038/nature11518. PMC 3538845. PMID 23060191.

Fluegel, Lucas L.; Hoye, Thomas R. (2021). "Hexadehydro-Diels–Alder Reaction: Benzyne Generation via Cycloisomerization of Tethered Triynes". Chem. Rev. 121 (4): 2413–2444. doi:10.1021/acs.chemrev.0c00825. PMC 8008985. PMID 33492939.

Minami, Atsushi; Oikawa, Hideaki (2016). "Recent advances of Diels–Alderases involved in natural product biosynthesis". The Journal of Antibiotics. 69 (7): 500–506. doi:10.1038/ja.2016.67. PMID 27301662. S2CID 30482282.

Behr, Arno (2000). "Organometallic Compounds and Homogeneous Catalysis". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a18_215. ISBN 978-3527306732.

Diels, O.; Alder, K. (1928). "Synthesen in der hydroaromatischen Reihe, I. Mitteilung: Anlagerungen von "Di-en"-kohlenwasserstoffen". Justus Liebigs Annalen der Chemie. 460: 98–122. doi:10.1002/jlac.19284600106.
Woodward, R. B.; Sondheimer, F.; Taub, D.; Heusler, K.; McLamore, W. M. (1952). "The Total Synthesis of Steroids". Journal of the American Chemical Society. 74 (17): 4223–4251. doi:10.1021/ja01137a001.
Corey, E. J.; Weinshenker, N. M.; Schaaf, T. K.; Huber, W. (1969). "Stereo-controlled synthesis of prostaglandins F-2a and E-2 (dl)". Journal of the American Chemical Society. 91 (20): 5675–7. doi:10.1021/ja01048a062. PMID 5808505.
Danishefsky, S.; Hirama, M.; Fritsch, N.; Clardy, J. (1979). "Synthesis of disodium prephenate and disodium epiprephenate. Stereochemistry of prephenic acid and an observation on the base-catalyzed rearrangement of prephenic acid to p-hydroxyphenyllactic acid". Journal of the American Chemical Society. 101 (23): 7013–7018. doi:10.1021/ja00517a039.
Wender, P. A.; Schaus, J. M.; White, A. W. (1980). "General methodology for cis-hydroisoquinoline synthesis: Synthesis of reserpine". Journal of the American Chemical Society. 102 (19): 6157–6159. doi:10.1021/ja00539a038.
Martin, S. F.; Rueger, H.; Williamson, S. A.; Grzejszczak, S. (1987). "General strategies for the synthesis of indole alkaloids. Total synthesis of (±)-reserpine and (±)-α-yohimbine". Journal of the American Chemical Society. 109 (20): 6124–6134. doi:10.1021/ja00254a036.
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.
Narasaka, K.; Shimada, S.; Osoda, K.; Iwasawa, N. (1991). "Phenylboronic Acid as a Template in the Diels-Alder Reaction". Synthesis. 1991 (12): 1171–1172. doi:10.1055/s-1991-28413.
Smith, A. B.; Sestelo, J. P.; Dormer, P. G. (1995). "Total Synthesis of (−)-Furaquinocin C". Journal of the American Chemical Society. 117 (43): 10755–10756. doi:10.1021/ja00148a023.
Kozmin, S. A.; Rawal, V. H. (1998). "A General Strategy to Aspidosperma Alkaloids: Efficient, Stereocontrolled Synthesis of Tabersonine". Journal of the American Chemical Society. 120 (51): 13523–13524. doi:10.1021/ja983198k.
Gibbs, R. A.; Okamura, W. H. (1988). "A short enantioselective synthesis of (+)-sterpurene: Complete intramolecular transfer of central to axial to central chiral elements". Journal of the American Chemical Society. 110 (12): 4062–4063. doi:10.1021/ja00220a069.
Charest, M. G.; Siegel, D. R.; Myers, A. G. (2005). "Synthesis of (-)-tetracycline". Journal of the American Chemical Society. 127 (23): 8292–3. doi:10.1021/ja052151d. PMID 15941256.
Dauben, W. G.; Kessel, C. R.; Takemura, K. H. (1980). "Simple, efficient total synthesis of cantharidin via a high-pressure Diels–Alder reaction". Journal of the American Chemical Society. 102 (22): 6893–6894. doi:10.1021/ja00542a060.
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.
Butz, L. W.; Rytina, A. W. (1949). "The Diels–Alder Reaction Quinones and Other Cyclenones". Organic Reactions. Vol. 5. pp. 136–192. doi:10.1002/0471264180.or005.03. ISBN 978-0471264187.
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.
Heintzelman, G. R.; Meigh, I. R.; Mahajan, Y. R.; Weinreb, S. W. (2005). "Diels-Alder Reactions of Imino Dienophiles". Organic Reactions. Vol. 65. pp. 141–599. doi:10.1002/0471264180.or065.02. ISBN 978-0471264187.
Ciganek, E. (1984). "The Intramolecular Diels-Alder Reaction". Organic Reactions. Vol. 32. pp. 1–374. doi:10.1002/0471264180.or032.01. ISBN 978-0471264187.

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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

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Corey, E. J.; Weinshenker, N. M.; Schaaf, T. K.; Huber, W. (1969). "Stereo-controlled synthesis of prostaglandins F-2a and E-2 (dl)". Journal of the American Chemical Society. 91 (20): 5675–7. doi:10.1021/ja01048a062. PMID 5808505.

Charest, M. G.; Siegel, D. R.; Myers, A. G. (2005). "Synthesis of (-)-tetracycline". Journal of the American Chemical Society. 127 (23): 8292–3. doi:10.1021/ja052151d. PMID 15941256.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

Ranganathan, S.; Ranganathan, D.; Mehrotra, A. K. (1977). "Ketene Equivalents". Synthesis. 1977 (5): 289–296. doi:10.1055/s-1977-24362. S2CID 260335918.

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Woodward, R. B.; Hoffmann, R. (22 October 2013). The conservation of orbital symmetry. Weinheim. ISBN 9781483282046. OCLC 915343522.{{cite book}}: CS1 maint: location missing publisher (link)