Journal articles on the topic 'Diels-Alder cycloaddition reactions'
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Grygorenko, Oleksandr O., Viktoriia S. Moskvina, Oleksandr V. Hryshchuk, and Andriy V. Tymtsunik. "Cycloadditions of Alkenylboronic Derivatives." Synthesis 52, no. 19 (June 24, 2020): 2761–80. http://dx.doi.org/10.1055/s-0040-1707159.
Full textBurnell, D. Jean, and Zdenek Valenta. "π-Facial stereoselectivity in the Diels–Alder reactions of a rigid carbocyclic diene: spiro(bicyclo[2.2.1]heptane-2,1′-[2,4]cyclopentadiene)." Canadian Journal of Chemistry 69, no. 1 (January 1, 1991): 179–84. http://dx.doi.org/10.1139/v91-028.
Full textSoares, Maria I. L., Ana L. Cardoso, and Teresa M. V. D. Pinho e Melo. "Diels–Alder Cycloaddition Reactions in Sustainable Media." Molecules 27, no. 4 (February 15, 2022): 1304. http://dx.doi.org/10.3390/molecules27041304.
Full textZhou, You-Yun, and Christopher Uyeda. "Catalytic reductive [4 + 1]-cycloadditions of vinylidenes and dienes." Science 363, no. 6429 (February 21, 2019): 857–62. http://dx.doi.org/10.1126/science.aau0364.
Full textZezula, Josef, Tomáš Hudlický, and Ion Ghiviriga. "Intramolecular Diels-Alder Cycloadditions of cis-Cyclohexadienediols Derived Enzymatically from (2-Azidoethyl)benzene. Construction of Highly Functionalized Bridged Isoquinoline Synthons." Collection of Czechoslovak Chemical Communications 66, no. 8 (2001): 1269–86. http://dx.doi.org/10.1135/cccc20011269.
Full textPratt, Andrew J., Phillip M. Rendle, and Peter J. Steel. "Anticancer Prodrug Studies: Diels - Alder Chemistry of 1-Methylthio-1-(p-tolylsulfonyl)ethene." Australian Journal of Chemistry 64, no. 7 (2011): 945. http://dx.doi.org/10.1071/ch10450.
Full textCarlini, Rina, Kerianne Higgs, Nicholas Taylor, and Russell Rodrigo. "Diels–Alder adducts of ortho-benzoquinones: rearrangements and further transformations." Canadian Journal of Chemistry 75, no. 6 (June 1, 1997): 805–16. http://dx.doi.org/10.1139/v97-097.
Full textAyadi, Sameh, and Manef Abderrabba. "Étude DFT des réactions de cycloaddition de type Diels–Alder sur le 4-aza-6-nitrobenzofuroxane." Canadian Journal of Chemistry 85, no. 5 (May 1, 2007): 331–35. http://dx.doi.org/10.1139/v07-026.
Full textPiers, Edward, Richard W. Friesen, Paul Kao, Steven J. Rettig, and James Trotter. "Synthesis of functionalized hexahydro-, octahydro-, and decahydro-1H-phenalenes via Diels–Alder reactions of 1-methylene-4a-methoxycarbonyl-1,2,3,4,4a,5,6,7-octahydronaphthalene and related dienes." Canadian Journal of Chemistry 71, no. 9 (September 1, 1993): 1463–83. http://dx.doi.org/10.1139/v93-188.
Full textKotha, Sambasivarao, Milind Meshram, and Nageswara Panguluri. "Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions." Synthesis 51, no. 09 (March 25, 2019): 1913–22. http://dx.doi.org/10.1055/s-0037-1612418.
Full textCabrera-Trujillo, Jorge Juan, and Israel Fernández. "Understanding exo-selective Diels–Alder reactions involving Fischer-type carbene complexes." Organic & Biomolecular Chemistry 17, no. 11 (2019): 2985–91. http://dx.doi.org/10.1039/c9ob00132h.
Full textFallis, Alex G. "1998 Alfred Bader Award Lecture Tangents and targets: The synthetic highway from natural products to medicine." Canadian Journal of Chemistry 77, no. 2 (February 1, 1999): 159–77. http://dx.doi.org/10.1139/v98-233.
Full textCantín, Ángel, M. Victoria Gomez, and Antonio de la Hoz. "Diels–Alder reactions in confined spaces: the influence of catalyst structure and the nature of active sites for the retro-Diels–Alder reaction." Beilstein Journal of Organic Chemistry 12 (October 13, 2016): 2181–88. http://dx.doi.org/10.3762/bjoc.12.208.
Full textAronica, Laura, and Gianluigi Albano. "Cyclization Reactions for the Synthesis of Phthalans and Isoindolines." Synthesis 50, no. 06 (January 31, 2018): 1209–27. http://dx.doi.org/10.1055/s-0037-1609175.
Full textSu, Zhishan, and Chan Kyung Kim. "Trienamine catalysis for asymmetric Diels–Alder reactions of 2,4-dienones: a theoretical investigation." Organic & Biomolecular Chemistry 13, no. 22 (2015): 6313–24. http://dx.doi.org/10.1039/c5ob00797f.
Full textEscalante, Carlos H., Eder I. Martínez-Mora, Carlos Espinoza-Hicks, Alejandro A. Camacho-Dávila, Fernando R. Ramos-Morales, Francisco Delgado, and Joaquín Tamariz. "Highly selective Diels–Alder and Heck arylation reactions in a divergent synthesis of isoindolo- and pyrrolo-fused polycyclic indoles from 2-formylpyrrole." Beilstein Journal of Organic Chemistry 16 (June 17, 2020): 1320–34. http://dx.doi.org/10.3762/bjoc.16.113.
Full textYang, Zhongyue, Song Yang, Peiyuan Yu, Yanwei Li, Charles Doubleday, Jiyong Park, Ashay Patel, et al. "Influence of water and enzyme SpnF on the dynamics and energetics of the ambimodal [6+4]/[4+2] cycloaddition." Proceedings of the National Academy of Sciences 115, no. 5 (January 18, 2018): E848—E855. http://dx.doi.org/10.1073/pnas.1719368115.
Full textBreton, Gary W., and Kenneth L. Martin. "Exploring the Limits of Reactivity of N-Methyl-1,2,4-triazoline-3,5-dione (MeTAD) with Disubstituted Bicycloalkadienes in the Homo-Diels–Alder Reaction." Organics 4, no. 1 (December 31, 2022): 41–48. http://dx.doi.org/10.3390/org4010002.
Full textFulton, Brandon B., Alexia J. Hartzell, H. V. Rasika Dias, and Carl J. Lovely. "Room Temperature Diels–Alder Reactions of 4-Vinylimidazoles." Molecules 29, no. 8 (April 22, 2024): 1902. http://dx.doi.org/10.3390/molecules29081902.
Full textRao, Nagaraj. "ASYMMETRIC ORGANOCATALYSIS." INDIAN DRUGS 58, no. 10 (December 16, 2021): 5–6. http://dx.doi.org/10.53879/id.58.10.p0005.
Full textTejero, Alvaro G., María Carmona, Ricardo Rodríguez, Fernando Viguri, Fernando J. Lahoz, Pilar García-Orduña, and Daniel Carmona. "Synthesis of chiral-at-metal rhodium complexes from achiral tripodal tetradentate ligands: resolution and application to enantioselective Diels–Alder and 1,3-dipolar cycloadditions." RSC Advances 12, no. 53 (2022): 34704–14. http://dx.doi.org/10.1039/d2ra06982b.
Full textCharlton, James L., Guy L. Plourde, and Glenn H. Penner. "Asymmetric induction in Diels–Alder reactions of α-alkoxyorthoquinodimethanes." Canadian Journal of Chemistry 67, no. 6 (June 1, 1989): 1010–14. http://dx.doi.org/10.1139/v89-153.
Full textWilliams, C. Luke, Katherine P. Vinter, Chun-Chih Chang, Ruichang Xiong, Sara K. Green, Stanley I. Sandler, Dionisios G. Vlachos, Wei Fan, and Paul J. Dauenhauer. "Kinetic regimes in the tandem reactions of H-BEA catalyzed formation of p-xylene from dimethylfuran." Catalysis Science & Technology 6, no. 1 (2016): 178–87. http://dx.doi.org/10.1039/c5cy01320h.
Full textBădoiu, Andrei, Yasmin Brinkmann, Florian Viton, and E. Peter Kündig. "Asymmetric Lewis acid-catalyzed 1,3-dipolar cycloadditions." Pure and Applied Chemistry 80, no. 5 (January 1, 2008): 1013–18. http://dx.doi.org/10.1351/pac200880051013.
Full textDuret, Guillaume, Vincent Le Fouler, Philippe Bisseret, Vincent Bizet, and Nicolas Blanchard. "Diels-Alder and Formal Diels-Alder Cycloaddition Reactions of Ynamines and Ynamides." European Journal of Organic Chemistry 2017, no. 46 (September 8, 2017): 6816–30. http://dx.doi.org/10.1002/ejoc.201700986.
Full textBoger, Dale L., and Christine E. Brotherton. "Diels-alder cycloaddition reactions of cyclopropenone ketals." Tetrahedron 42, no. 11 (January 1986): 2777–85. http://dx.doi.org/10.1016/s0040-4020(01)90567-8.
Full textLaurent, Alain, Nidia P. Villalva-Servín, Pat Forgione, Peter D. Wilson, David V. Smil, and Alex G. Fallis. "Part 1: Efficient strategies for the construction of variably substituted bicyclo[5.3.1]undecenones (AB taxane ring systems)." Canadian Journal of Chemistry 82, no. 2 (February 1, 2004): 215–26. http://dx.doi.org/10.1139/v03-200.
Full textTomé, Augusto C., Maria G. P. M. S. Neves, and José A. S. Cavaleiro. "Porphyrins and other pyrrolic macrocycles in cycloaddition reactions." Journal of Porphyrins and Phthalocyanines 13, no. 04n05 (April 2009): 408–14. http://dx.doi.org/10.1142/s1088424609000619.
Full textHou, Ji-Qin, Jiang-Hong Yu, Heng Zhao, Ying-Ying Dong, Qiu-Shi Peng, Bao-Bao Zhang, and Hao Wang. "Biomimetic total syntheses of baefrutones A–D, baeckenon B, and frutescones A, D–F." Organic & Biomolecular Chemistry 18, no. 6 (2020): 1135–39. http://dx.doi.org/10.1039/c9ob02490e.
Full textBednarek, Melania, and Przemysław Kubisa. "Reversible networks of degradable polyesters containing weak covalent bonds." Polymer Chemistry 10, no. 15 (2019): 1848–72. http://dx.doi.org/10.1039/c8py01731j.
Full textBauer, John B., Fatima Diab, Cäcilia Maichle-Mössmer, Hartmut Schubert, and Holger F. Bettinger. "Synthesis of the [11]Cyclacene Framework by Repetitive Diels–Alder Cycloadditions." Molecules 26, no. 10 (May 20, 2021): 3047. http://dx.doi.org/10.3390/molecules26103047.
Full textPetko, Dina, Matthew Stratton, and William Tam. "Ruthenium-catalyzed Bis-Homo-Diels-Alder reaction: searching for commercially available catalysts and expanding the scope of reaction." Canadian Journal of Chemistry 96, no. 12 (December 2018): 1115–21. http://dx.doi.org/10.1139/cjc-2018-0117.
Full textHamzehloueian, Mahshid, Saeid Yeganegi, Yaghoub Sarrafi, Kamal Alimohammadi, and Marzieh Sadatshahabi. "A theoretical investigation on the regioselectivity of the intramolecular hetero Diels-Alder and 1,3-dipolar cycloaddition of 2-vinyloxybenzaldehyde derivatives." Journal of the Serbian Chemical Society 79, no. 8 (2014): 911–24. http://dx.doi.org/10.2298/jsc140121012h.
Full textJursic, Branko S. "AM1 semiempirical study of benzopyrroles as dienes for Diels-Alder reaction." Canadian Journal of Chemistry 74, no. 1 (January 1, 1996): 114–20. http://dx.doi.org/10.1139/v96-015.
Full textBrossard, Dominique, Pascal Retailleau, Vincent Dumontet, Philippe Breton, Sandy Desrat, and Fanny Roussi. "Fast & easy preparation of 3D scaffolds from methyl benzoate by a diversity oriented synthesis strategy based on Diels–Alder and ene-reactions." Organic & Biomolecular Chemistry 15, no. 26 (2017): 5585–92. http://dx.doi.org/10.1039/c7ob01236e.
Full textKoçak, Ramazan, and Arif Daştan. "Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles." Beilstein Journal of Organic Chemistry 17 (March 15, 2021): 719–29. http://dx.doi.org/10.3762/bjoc.17.61.
Full textGribble, G. W. "Novel chemistry of indole in the synthesis of heterocycles." Pure and Applied Chemistry 75, no. 10 (January 1, 2003): 1417–32. http://dx.doi.org/10.1351/pac200375101417.
Full textÇapan, İrfan, and Süleyman Servi. "Synthesis of New C2-Symmetric Chiral Benzimidazole Derivatives Having Norbornene/Dibenzobarrelene Skeletons." Letters in Organic Chemistry 17, no. 10 (November 17, 2020): 801–5. http://dx.doi.org/10.2174/1570178616666190731105327.
Full textMlostoń, Grzegorz, Yuriy Shermolovich, and Heinz Heimgartner. "Synthesis of Fluorinated and Fluoroalkylated Heterocycles Containing at Least One Sulfur Atom via Cycloaddition Reactions." Materials 15, no. 20 (October 17, 2022): 7244. http://dx.doi.org/10.3390/ma15207244.
Full textKorol, Nataliya, Mikhailo Slivka, and Oksana Holovko-Kamoshenkova. "Cycloaddition reactions of 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione (PTAD) and 4-methyl-3H-1,2,4-triazole-3,5(4H)-dione (MTAD): A short review." Organic Communications 13, no. 4 (December 26, 2020): 146–54. http://dx.doi.org/10.25135/acg.oc.88.20.11.1870.
Full textBeck, Janina, Olaf Fuhr, Martin Nieger, and Stefan Bräse. "A versatile Diels–Alder approach to functionalized hydroanthraquinones." Royal Society Open Science 7, no. 11 (November 2020): 200626. http://dx.doi.org/10.1098/rsos.200626.
Full textSpino, Claude, and Jason Crawford. "2-Carbomethoxy-1,3-butadiene: an electronically activated diene in [4 + 2] cycloadditions with electron-deficient dienophiles." Canadian Journal of Chemistry 71, no. 7 (July 1, 1993): 1094–97. http://dx.doi.org/10.1139/v93-145.
Full textBates, Robert W., Andrew J. Pratt, Phillip M. Rendle, and Ward T. Robinson. "Diels - Alder Reactions of 1,1-Bis(methylthio)ethene with Pyran-2-ones." Australian Journal of Chemistry 51, no. 5 (1998): 383. http://dx.doi.org/10.1071/c97128.
Full textMoore, Jonathan C., E. Stephen Davies, Darren A. Walsh, Pallavi Sharma, and John E. Moses. "Formal synthesis of kingianin A based upon a novel electrochemically-induced radical cation Diels–Alder reaction." Chem. Commun. 50, no. 83 (2014): 12523–25. http://dx.doi.org/10.1039/c4cc05906a.
Full textde Sousa, Andrea L. F., José E. P. Cardoso Filho, Blanka Wladislaw, Liliana Marzorati, and Claudio Di Vitta. "Studies on chemo- and diastereo-selectivity of the Diels–Alder reactions of sulfinyltoluquinones with cyclopentadiene." Canadian Journal of Chemistry 87, no. 8 (August 2009): 1135–43. http://dx.doi.org/10.1139/v09-070.
Full textCharlton, James L., and Shawn Maddaford. "The mechanism of stereoselectivity in the cycloaddition reactions of α-hydroxy-ortho-quinodimethanes with the fumarate of methyl lactate and mandelate." Canadian Journal of Chemistry 71, no. 6 (June 1, 1993): 827–33. http://dx.doi.org/10.1139/v93-110.
Full textZeller, Matthias, Allen D. Hunter, Paul Sampson, and Nataliya Chumachenko. "1-[(E)-Butadienylsulfonyl]-3,3-dimethylbut-2-yl methacrylate." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 15, 2006): o1369—o1370. http://dx.doi.org/10.1107/s1600536806008014.
Full textGillard, James R., Michael J. Newlands, John N. Bridson, and D. Jean Burnell. "π-Facial stereoselectivity in the Diels–Alder reactions of benzene oxides." Canadian Journal of Chemistry 69, no. 9 (September 1, 1991): 1337–43. http://dx.doi.org/10.1139/v91-199.
Full textJasiński, Radomir. "On the Question of Stepwise [4+2] Cycloaddition Reactions and Their Stereochemical Aspects." Symmetry 13, no. 10 (October 11, 2021): 1911. http://dx.doi.org/10.3390/sym13101911.
Full textWard, Dale E., Thomas E. Nixey, Yuanzhu Gai, Matthew J. Hrapchak, and M. Saeed Abaee. "Intramolecular Diels–Alder reactions of 2H-thiopyran dienes." Canadian Journal of Chemistry 74, no. 7 (July 1, 1996): 1418–36. http://dx.doi.org/10.1139/v96-160.
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